{"title":"Molecular \u0026 Immunodiagnostics","description":"","products":[{"product_id":"sera-mag-select-60ml","title":"Sera-Mag Select 60ml","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nCombines the exceptional binding characteristics of Sera-Mag Carboxyl Speedbeads with an optimized binding solution in a ready-to-use formulation.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Use a single reagent for PCR clean-up and size selection.\u003cbr\u003e\r\n•Easily control what size DNA is retained or eliminated by adding various ratios of Sera-Mag Select to your sample. This enables NGS library and PCR fragment clean-up, as well as dual size selection of libraries.\u003cbr\u003e\r\n•Uses the same protocols as existing reagents so can be directly integrated into existing workflows with minimal disruption.\u003cbr\u003e\r\n•Sera-Mag Select delivers tight distribution in size selection for high yield recovery of specific fragment sizes.\u003cbr\u003e\r\n•Suitable for manual, high throughput, and automated workflows.\u003cbr\u003e\r\n•Sera-Mag Select should be stored in the refrigerator between 2°C to 8°C. Do not freeze. Store upright and keep bottle tightly sealed.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is a Sample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775944446243,"sku":"CYTI29343052","price":987.7,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29453302.jpg?v=1789945814"},{"product_id":"amersham-hot-start-master-mix","title":"Amersham Hot Start Master Mix","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nHot Start Master Mix is a 2X premixed formulation that can effectively reduce nonspecific priming and primer-dimer formation during PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\nRecombinant hot start activator protein sequesters primers prior to PCR, effectively reducing nonspecific priming and primer-dimer formation.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Quick hot start activation preserves sample integrity by avoiding extensive precycling heat treatment.\u003cbr\u003e\r\n•Avoids the risk of contamination from a mammalian source associated with hot start antibodies.\u003cbr\u003e\r\n•Convenient, ready-to-use mix saves time and reduces experimental variability.\u003cbr\u003e\r\n•Confidence in downstream applications; increased read length in sequencing applications.\u003cbr\u003e\r\n•For any standard PCR reaction, such as multiplex PCR, and reactions exhibiting nonspecific amplification or primer-dimer formation.\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription\u003cbr\u003e\r\nHot Start Master Mix uses a novel hot start method called primer sequestration.\u003cbr\u003e\r\n\u003cbr\u003e\r\nHot Start Master Mix combines high-quality recombinant Taq DNA Polymerase, a recombinant hot start activator protein, and nucleotides in a proprietary reaction buffer. This ready-to-use mix provides robust and reliable performance for demanding PCR applications in which high specificity and high sensitivity are essential to success. The mix does not contain Taq antibody and this eliminates the risk of contamination from a mammalian source. Also, since the polymerase is not chemically inactivated, there is no extensive precycling heating step necessary; this reduces the chance of damaging precious DNA samples from heat-induced depurination. The net result from using Hot Start Master Mix is a more robust and reliable amplification of the target amplicons with increased yield when compared to conventional hot start master mix products.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775944577315,"sku":"CYTI25150001","price":229.6,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/25150001.jpg?v=1789940416"},{"product_id":"amersham-microspin-s-300-hr-columns","title":"Amersham MicroSpin S-300 HR Columns","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nMicroSpin S-300 HR spin columns for DNA purification from unincorporated primers (\u0026lt;20-mers) and nucleotides using spin-column chromatography in applications including desalting, buffer exchange, and primer removal.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAccommodates 25 to 50 µL: for post-PCR cleanup prior to sequencing\u003cbr\u003e\r\n•Useful for purification: for example, alkaline-denatured plasmid DNA prior to sequencing\u003cbr\u003e\r\n•Convenient: prepacked with Sephacryl™ S-300 HR pre-equilibrated in TE (Tris\/EDTA) buffer\u003cbr\u003e\r\n•Ready to use: requires less than 4 minutes from sample application through to collection of purified product\u003cbr\u003e\r\n•Tested in assays: nickase, single- and double-stranded exonuclease, and RNase\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin columns are designed for rapid nucleic acid purification for use in a wide range of applications, including desalting, buffer exchange and primer removal. Good product yield and purity are obtained with sample volumes from 25-100 µL, and from nanogram to milligram quantities of DNA.\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin S-200, S-300 and S-400 HR spin columns contain Sephacryl resin of differing pore sizes. They allow DNA purification via gel filtration. Molecules larger than the largest pores in the Sephacryl are excluded from the gel and elute first. Intermediate size molecules penetrate the matrix to varying extents, depending on their size and the resin used. Penetration of the matrix retards progress through the spin column; very small molecules elute last. The volume required to elute these small molecules is dependent on the volume available both inside and outside the pores, i.e. the bed volume.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775944839459,"sku":"CYTI27513001","price":367.8,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27513001.jpg?v=1789940716"},{"product_id":"amersham-microspin-s-400-hr-columns","title":"Amersham MicroSpin S-400 HR Columns","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nMicroSpin S-300 HR spin columns for DNA purification from unincorporated primers (\u0026lt;20-mers) and nucleotides using spin-column chromatography in applications including desalting, buffer exchange, and primer removal.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Accommodates 25 to 50 µL: for post-PCR cleanup prior to sequencing\u003cbr\u003e\r\n•Useful for purification: for example, alkaline-denatured plasmid DNA prior to sequencing\u003cbr\u003e\r\n•Convenient: prepacked with Sephacryl™ S-300 HR pre-equilibrated in TE (Tris\/EDTA) buffer\u003cbr\u003e\r\n•Ready to use: requires less than 4 minutes from sample application through to collection of purified product\u003cbr\u003e\r\n•Tested in assays: nickase, single- and double-stranded exonuclease, and RNase\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin columns are designed for rapid nucleic acid purification for use in a wide range of applications, including desalting, buffer exchange and primer removal. Good product yield and purity are obtained with sample volumes from 25-100 µL, and from nanogram to milligram quantities of DNA.\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin S-200, S-300 and S-400 HR spin columns contain Sephacryl resin of differing pore sizes. They allow DNA purification via gel filtration. Molecules larger than the largest pores in the Sephacryl are excluded from the gel and elute first. Intermediate size molecules penetrate the matrix to varying extents, depending on their size and the resin used. Penetration of the matrix retards progress through the spin column; very small molecules elute last. The volume required to elute these small molecules is dependent on the volume available both inside and outside the pores, i.e. the bed volume.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775944937763,"sku":"CYTI27514001","price":391.3,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27514001.jpg?v=1789940718"},{"product_id":"templiphi-500-amplification-kit-500-reactions","title":"TempliPhi 500 amplification kit, 500 reactions","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nTempliPhi™, based on Phi29 DNA polymerase, is used to exponentially amplify single- or double-stranded circular DNA by rolling circle amplification (RCA).\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Prepare templates for cycle sequencing, cloning, and transformation from circular DNA starting material efficiently, in 4 to 6 hours\u003cbr\u003e\r\n•Generate microgram quantities of template DNA from picogram amounts of circular DNA\u003cbr\u003e\r\n•Use amplified DNA directly for cycle sequencing without purification\u003cbr\u003e\r\n•Amplify DNA from bacterial or M13 liquid cultures, colonies, plaques, glycerol stocks, or purified circular (plasmid or M13) DNA\u003cbr\u003e\r\n•Reduces time, labor, and quantity of consumables needed for sequencing template preparation\u003cbr\u003e\r\n•Allows easy automation of workflow for efficient low- to medium-throughput small DNA vector preparation\u003cbr\u003e\r\n\u003cbr\u003e\r\nTrends in rolling circle amplification: Capabilities for manipulation, error free production and assembly of nucleic acids are advancing. \u003cbr\u003e\r\n\u003cbr\u003e\r\nOne-tube, one-temperature format\u003cbr\u003e\r\nTempliPhi™ kits use a unique kind of circular DNA amplification to efficiently prepare micrograms of DNA from picogram circular DNA starting material. TempliPhi™ kits use isothermal rolling circle amplification (RCA) for the exponential amplification of circular DNA using bacteriophage Phi29 DNA polymerase. The amplification used is often called multiple strand displacement amplification, or MDA. Phi29 DNA polymerase is active at 30°C, and isothermal amplification is performed at this temperature without the need for thermal cycling. The TempliPhi™ protocol allows amplification of 96 samples from bacterial colonies with less than 20 min of hands-on time.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTwo different types of TempliPhi™ DNA Amplification Kits are available to meet different throughput requirements. TempliPhi™ DNA Amplification Kit for 2000 reactions, designed for automation, contains pre-mixed components and requires overnight incubation. TempliPhi™ 100 and TempliPhi™ 500 reaction kits contain separate, unmixed components for enhanced stability and preparations are ready in 4 to 6 hours.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945003299,"sku":"CYTI25640050","price":1869.6,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/25640050.jpg?v=1789940721"},{"product_id":"autoseq-g-50-250-columns","title":"AutoSeq G-50, 250 columns","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nAutoSeq G-50 columns are specifically designed to remove fluorescent dye-terminators from cycle sequencing reactions prior to analysis on automated sequencers.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For rapid removal of unincorporated fluorescent dye-terminators from cycle sequencing reactions prior to automated DNA sequencing\u003cbr\u003e\r\n•Columns are prepacked with Sephadex G-50 DNA Grade F\u003cbr\u003e\r\n•Columns are pre-equilibrated in double-distilled water with 0.05% Kathon CG\/ICP Biocide added as a preservative\u003cbr\u003e\r\n•Ready-to-use columns enable sample application through to collection of purified product in less than 4 min\u003cbr\u003e\r\n•4 minutes\u003cbr\u003e\r\n\u003cbr\u003e\r\nEffective DNA purification is essential for high-quality results on automated DNA sequencing since residual dye-terminators can obscure data.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAutoSeq G-50 consists of MicroSpin columns containing Sephadex G-50 DNA Grade F, pre-equilibrated in double-distilled water. This is important because even the small amount of salt in traditional buffers (such as TE buffer) can cause electrophoretic artefacts on salt-sensitive automated DNA sequencers.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is a Sample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945101603,"sku":"CYTI27534002","price":1247.9,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27534003.jpg?v=1789940724"},{"product_id":"amersham-ready-to-go-rt-pcr-beads-0-2-ml-hinged-tube-with-cap-96-reactions","title":"Amersham Ready-To-Go RT-PCR Beads (0.2ml Hinged Tube with Cap), 96 reactions","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nPre-dispensed, freeze-dried beads that include the reagents necessary for one-step reverse transcription-PCR with high sensitivity and reproducibility.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Preformulated, predispensed, single-dose, ambient-temperature-stable beads ensure greater reproducibility between reactions, minimize pipetting steps, and reduce the potential for pipetting errors and contamination.\u003cbr\u003e\r\n•Optimized as a one-tube, one-step RT-PCR reaction for both cDNA synthesis and PCR.\u003cbr\u003e\r\n•Each lot of RT-PCR Beads is function tested for its ability to generate highly specific PCR products to ensure lot-to-lot reproducibility\u003cbr\u003e\r\n•For highly reproducible one-step reverse transcription-PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription\u003cbr\u003e\r\nReady-To-Go RT-PCR Beads are stable at room temperature and designed for performing single-tube one-step reverse transcription-PCR. Each room-temperature-stable bead contains M-MuLV Reverse Transcriptase, RNase Inhibitor, buffer, nucleotides, and Taq DNA Polymerase. The only additional reagents required are water, template RNA, and primers. The reagents are optimized for full-length cDNA synthesis to \u0026gt;7.5 kb and optimal sensitivity from PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe Ready-To-Go Bead format significantly reduces the number of pipetting steps, thereby increasing reproducibility of the RT-PCR technique and minimizing risk of contamination and RNA degradation. Ready-To-Go RT-PCR Beads are provided in either thin walled 0.5 ml or 0.2 ml tubes compatible with most thermocyclers. The 0.2 ml tubes come assembled in a 96-well (8 × 12) plate format that allows individual strips of eight tubes to be easily removed. This flexibility allows use of either the entire 96-well plate, strips of eight or individual 0.2 ml tubes. Each package of Ready-To-Go RT-PCR Beads contains: RT-PCR beads, control reactions and pd(N)6 and oligo(dT) cDNA primers.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945199907,"sku":"CYTI27925901","price":659.7,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27925901.jpg?v=1789940726"},{"product_id":"exoprostar-5000-reactions","title":"ExoProStar, 5000 reactions (US78225)","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nEnzymatic PCR clean up technology with Exonuclease I and Alkaline Phosphatase to remove unincorporated primers and dNTPs. For maximum flexibility comes in two separate tubes.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Enzymes optimized to work together for high efficiency removal of unincorporated primers and nucleotides.\u003cbr\u003e\r\n•Enzymes provided in two separate tubes; just two simple pipetting steps are needed to prepare the reaction.\u003cbr\u003e\r\n•Fast 30 min protocol.\u003cbr\u003e\r\n•Scalable for different reaction sizes.\u003cbr\u003e\r\n•No loss of PCR product.\u003cbr\u003e\r\n•Easy to automate.\u003cbr\u003e\r\n•Complete heat inactivation of the enzymes within 15 min.\u003cbr\u003e\r\n\u003cbr\u003e\r\nExoProStar is our new name for this PCR clean-up technology. No change in the formulation, so you get the same great product, and same great benefits!\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe ExoProStar PCR and Sequence Reaction Clean-Up Kit updates existing enzymatic PCR clean up technology with Exonuclease I and Alkaline Phosphatase to remove unincorporated primers and dNTPs. ExoProStar improves digestion efficiency with no degradation of the target PCR product. Your sample is completely intact and ready for immediate use in manual or automated processes.\u003cbr\u003e\r\n\u003cbr\u003e\r\nFor the convenience of a single, stable enzyme mix with just one pipetting step we also offer the ExoProStar 1-Step (not sold in the USA, Canada or Japan).\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945298211,"sku":"CYTI29002101","price":3674.1,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29002090_9494bc2f-3d37-47cc-9d7a-170a8a91b0af.jpg?v=1789945514"},{"product_id":"amersham-microspin-s-200-hr-columns","title":"Amersham MicroSpin S-200 HR Columns","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nMicroSpin S-200 HR spin columns for rapid DNA purification of labeled single-stranded or double-stranded DNA fragments =50 bases in length in applications including desalting, buffer exchange, and primer removal using spin-column chromatography.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Prepacked with Sephacryl™ S-200 HR resin pre-equilibrated in TE (Tris\/EDTA) buffer\u003cbr\u003e\r\n•\u0026gt;80% sample recovery\u003cbr\u003e\r\n•Tested in nickase, single- and double-stranded exonuclease, and RNase assays\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin columns are designed for rapid nucleic acid purification for use in a wide range of applications, including desalting, buffer exchange and removal of primers. Good product yield and purity are obtained with sample volumes from 25-100 µL, and from nanogram to milligram quantities of DNA.\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin S-200, S-300 and S-400 HR spin columns contain Sephacryl resin of differing pore sizes. They allow DNA purification by the process of gel filtration. Molecules larger than the largest pores in the Sephacryl are excluded from the gel and elute first. Intermediate size molecules penetrate the matrix to varying extents, depending on their size and the resin used. Penetration of the matrix retards progress through the column; very small molecules elute last. The volume required to elute these small molecules is dependent on the volume available both inside and outside the pores i.e. the bed volume.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945429283,"sku":"CYTI27512001","price":567.5,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27512001.jpg?v=1789940729"},{"product_id":"sera-xtracta-virus-pathogen-kit","title":"Sera-Xtracta Virus\/Pathogen Kit","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nSera-Xtracta™ Virus\/Pathogen Kit for high-throughput total nucleic acid (DNA\/RNA) isolation from bacteria and viruses including Adenovirus (Type 14), Influenza A (H3N2) and COVID-19.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Offers the advantages of solid phase extraction (using magnetic beads) and reproducible yields.\u003cbr\u003e\r\n•Simplified protocol can be adapted for both manual and automated high-throughput processing.\u003cbr\u003e\r\n•Scalable up to 400 µL of sample.\u003cbr\u003e\r\n•Rapid extraction procedure can be completed in less than 30 minutes.\u003cbr\u003e\r\n•For use with respiratory biological matrices, blood and universal transport media to support the sensitive downstream detection of viruses and other pathogens found in low concentrations.\u003cbr\u003e\r\n•Compatible with molecular biology techniques, including quantitative polymerase chain reaction (qPCR, RT-qPCR), droplet digital PCR (ddPCR), and next-generation sequencing (NGS).\u003cbr\u003e\r\n\u003cbr\u003e\r\nSera-Xtracta Virus\/Pathogen Kit provides a simple and rapid method to optimize the workflow for sensitive detection of viruses and other pathogens found in low concentrations.\u003cbr\u003e\r\n\u003cbr\u003e\r\nInfectious diseases affect millions of people every year. Particularly virulent and multi-drug resistant agents are increasingly responsible for infections with ever-expanding complexities. The design, manufacture and validation of assays for these pathogenic agents requires the successful purification of high-quality nucleic acid. This is essential to any molecular research and testing workflow. The nucleic acid purification process can be a bottleneck because sufficient nucleic acid from biological samples is required to meet a sensitivity threshold for assays which are designed to help identify, map or make informed decisions on latent and active infections.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe Sera-Xtracta Virus\/Pathogen kit is for research use only (RUO).\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945494819,"sku":"CYTI29506009","price":491.6,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29506009.jpg?v=1789946115"},{"product_id":"amersham-nick-columns","title":"Amersham NICK Columns","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\n\u003cbr\u003e\r\nNICK Columns are used for the purification of nick-translated DNA fragments and for separation of any labeled probe from unincorporated labeled nucleotides.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For rapid purification of labeled DNA (= 20 bases in length) from unincorporated radiolabeled nucleotides using gravity-flow chromatography.\u003cbr\u003e\r\n•Prepacked with Sephadex G-50 DNA Grade (see Sephadex G-50 DNA Grade and Sephadex G-100 DNA Grade) in distilled water with 0.15% Kathon CG\/ICP Biocide\u003cbr\u003e\r\n•Can accommodate sample volumes up to 100 µl\u003cbr\u003e\r\n\u003cbr\u003e\r\nNICK columns are ready for immediate use and operate by gravity flow. Tests show that at least 97% of radioactivity applied in a nick-translated mixture elutes in two well-separated peaks, corresponding to labeled DNA molecules and unincorporated nucleotides, respectively. At least 90% of the applied DNA is recovered and can then be used in DNA hybridization protocols. Maximum sample volume is 100 µL.\u003cbr\u003e\r\n\u003cbr\u003e\r\nNick translation is a technique in which DNA Polymerase I is used to replace some of the nucleotides of a DNA sequence with their labeled analogues, creating a tagged DNA sequence which can be used as a probe in fluorescent in situ hybridization (FISH) or blotting techniques. It can also be used for radioactive labeling in techniques such as Southern blotting.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThis process is called nick translation because the DNA to be labelled is treated with DNase to produce single-stranded \"nicks.\" This is followed by replacement in nicked sites by DNA polymerase I, which elongates the 3' end, removing nucleotides by 5'-3' exonuclease activity, and replacing them with dNTPs. To label a DNA fragment for use as a probe in blotting one of the incorporated nucleotides provided in the reaction is radiolabeled, or a fluorophore can be attached instead for fluorescent labelling, or is used as an antigen for immunodetection.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-50 DNA Grade can be used in a wide range of applications, including desalting DNA, buffer exchange, and removal of unincorporated nucleotides from end-labelled oligonucleotides. Sephadex G-50 can be packed into empty MicroSpin columns for use in these applications.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-50 is one of five different G-types ranging from G-10 for small molecules to G-75 for larger molecules. Sephadex G-50 is a well-established gel filtration resin for desalting and buffer exchange of biomolecules \u0026gt; 30 000 molecular weight, and with a spin protocol can be used for DNA and oligo purification of molecules greater than 20 bases in length. Alternatively, Sephadex G-25 can be used. Sephadex G-25 has an exclusion limit of approximately Mr 5000, and with a spin protocol this means it can be used for any DNA greater than 10 bases in length.\u003cbr\u003e\r\n\u003cbr\u003e\r\nBoth types of Sephadex are therefore highly suitable for the purification of oligonucleotides or very small DNA fragments following synthesis or in radioactive labeling.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-25 DNA Grade and Sephadex G-50 DNA Grade are sold separately.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945593123,"sku":"CYTI17085502","price":668.7,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/17085502.png?v=1781219539"},{"product_id":"sera-mag-select-450ml","title":"Sera-Mag Select 450ml","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nCombines the exceptional binding characteristics of Sera-Mag Carboxyl Speedbeads with an optimized binding solution in a ready-to-use formulation.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Use a single reagent for PCR clean-up and size selection.\u003cbr\u003e\r\n•Easily control what size DNA is retained or eliminated by adding various ratios of Sera-Mag Select to your sample. This enables NGS library and PCR fragment clean-up, as well as dual size selection of libraries.\u003cbr\u003e\r\n•Uses the same protocols as existing reagents so can be directly integrated into existing workflows with minimal disruption.\u003cbr\u003e\r\n•Sera-Mag Select delivers tight distribution in size selection for high yield recovery of specific fragment sizes.\u003cbr\u003e\r\n•Suitable for manual, high throughput, and automated workflows.\u003cbr\u003e\r\n•Sera-Mag Select should be stored in the refrigerator between 2°C to 8°C. Do not freeze. Store upright and keep bottle tightly sealed.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is a Sample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945658659,"sku":"CYTI29343057","price":5609.7,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29453302_c63e7a0a-44c7-48f1-a833-71104de5baf7.jpg?v=1789945817"},{"product_id":"exonuclease-i-2500-units","title":"Exonuclease I, 2500 Units","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nExonuclease I is used to selectively digest excess single stranded DNA in a mixture also containing double-stranded DNA, such as removing unused primers after PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•3''-5'' single-stranded exonuclease.\u003cbr\u003e\r\n•Monomeric 54.5 kDa bacterial exonuclease I recombinantly expressed in E. coli.\u003cbr\u003e\r\n•Inactivated by heating at 80°C for 15 minutes.\u003cbr\u003e\r\n•Active in PCR buffers.\u003cbr\u003e\r\n\u003cbr\u003e\r\nExonuclease I, used together with Alkaline Phosphatase for inactivation of dNTPs, provides effective cleanup of PCR reactions for subsequent use in DNA sequencing.\u003cbr\u003e\r\n\u003cbr\u003e\r\nDigestion of single stranded DNA by Exonuclease I releases dNTPs leaving 5''-terminal dinucleotides intact. DNA strands with terminal 3''-OH groups blocked by phosphoryl or acetyl groups are not removed.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945756963,"sku":"CYTI25003930","price":187.5,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27700734.jpg?v=1789940418"},{"product_id":"amersham-ready-to-go-rt-pcr-beads-0-2-ml-tubes-96-reactions","title":"Amersham Ready-To-Go RT-PCR Beads (0.2ml Tubes), 96 reactions","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nPre-dispensed, freeze-dried beads that include the reagents necessary for one-step reverse transcription-PCR with high sensitivity and reproducibility.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Preformulated, predispensed, single-dose, ambient-temperature-stable beads ensure greater reproducibility between reactions, minimize pipetting steps, and reduce the potential for pipetting errors and contamination.\u003cbr\u003e\r\n•Optimized as a one-tube, one-step RT-PCR reaction for both cDNA synthesis and PCR.\u003cbr\u003e\r\n•Each lot of RT-PCR Beads is function tested for its ability to generate highly specific PCR products to ensure lot-to-lot reproducibility\u003cbr\u003e\r\n•For highly reproducible one-step reverse transcription-PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription\u003cbr\u003e\r\nReady-To-Go RT-PCR Beads are stable at room temperature and designed for performing single-tube one-step reverse transcription-PCR. Each room-temperature-stable bead contains M-MuLV Reverse Transcriptase, RNase Inhibitor, buffer, nucleotides, and Taq DNA Polymerase. The only additional reagents required are water, template RNA, and primers. The reagents are optimized for full-length cDNA synthesis to \u0026gt;7.5 kb and optimal sensitivity from PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe Ready-To-Go Bead format significantly reduces the number of pipetting steps, thereby increasing reproducibility of the RT-PCR technique and minimizing risk of contamination and RNA degradation. Ready-To-Go RT-PCR Beads are provided in either thin walled 0.5 ml or 0.2 ml tubes compatible with most thermocyclers. The 0.2 ml tubes come assembled in a 96-well (8 × 12) plate format that allows individual strips of eight tubes to be easily removed. This flexibility allows use of either the entire 96-well plate, strips of eight or individual 0.2 ml tubes. Each package of Ready-To-Go RT-PCR Beads contains: RT-PCR beads, control reactions and pd(N)6 and oligo(dT) cDNA primers.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945888035,"sku":"CYTI27926701","price":666.0,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27925901_070126ea-dc0b-4928-863f-968fc9278835.jpg?v=1789940732"},{"product_id":"amersham-ready-to-go-rapd-analysis-kit-100-reactions-and-6-primers","title":"Amersham Ready-To-Go RAPD Analysis Kit (100 reactions and 6 primers)","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nRAPD analysis is a technique for rapidly detecting genomic polymorphisms. A single short oligonucleotide primer of arbitrary sequence is used under low stringency conditions in PCR to generate a reproducible array of strain-specific products.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For performing DNA profiling experiments using the randomly amplified polymorphic DNA [RAPD (1)] technique.\u003cbr\u003e\r\n•Preformulated, predispensed, single-dose reaction beads are provided as ambient-temperature-stable beads to ensure greater reproducibility between reactions, minimize pipetting steps and reduce the potential for pipetting errors and contamination.\u003cbr\u003e\r\n•RAPD* reactions are simple to perform—simply add genomic DNA solution and primer to a tube of RAPD Analysis Beads to a final reaction volume of 25 µl and cycle the reaction.\u003cbr\u003e\r\nEach lot of RAPD Analysis Beads is function-tested to ensure its ability to generate a differential banding pattern between the two control E. coli strains using RAPD Analysis Primer 2 included with the RAPD beads.\u003cbr\u003e\r\n•RAPD reactions are pre-optimized for use with a wide variety of organisms.\u003cbr\u003e\r\n\u003cbr\u003e\r\n\u003cbr\u003e\r\nReady-To-Go RAPD Analysis Beads are designed as premixed , predispensed reactions for performing random amplified polymorphic DNA (RAPD) analysis. With RAPD analysis, genomic polymorphisms can be detected at multiple loci using only nanogram quantities of DNA. The RAPD reactions are provided as room-temperature-stable dried beads that contain all the necessary reagents, except primer, for performing RAPD analysis.\u003cbr\u003e\r\n\u003cbr\u003e\r\nRAPD analysis is a technique for rapidly detecting genomic polymorphisms. A single, short oligonucleotide primer of arbitrary sequence is used under low stringency conditions in PCR to generate a reproducible array of strain-specific products that are analyzed by gel electrophoresis. Under these conditions, genomic polymorphisms can be detected at multiple loci using only nanogram quantities of DNA. RAPD analysis has been used in numerous applications, including gene mapping, detection of strain diversity, population analysis, epidemiology and the analysis of phylogenetic and taxonomic relationships (2).\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe RAPD reactions are provided as dried beads that contain all the necessary PCR components, except primer, in concentrations optimized for RAPD analysis. Beads are provided in thin-walled 0.5 ml tubes compatible with most thermal cyclers. Each package of Ready-To-Go RAPD Analysis Beads contains sufficient reagents for 100 individual RAPD reactions: RAPD analysis beads, control E. coli BL21 DNA, control E. coli C1a DNA, RAPD analysis primer 2, and instruction booklet (DNA from two E. coli strains and RAPD analysis primer 2 are provided as controls to assay the ability of the RAPD beads to amplify DNA and identify polymorphisms).\u003cbr\u003e\r\n\u003cbr\u003e\r\nRAPD Analysis Kit consists of Ready-To-Go RAPD Analysis Beads and six primers that can be used with RAPD Analysis Beads. Each primer in the set is an arbitrary 10-mer that is specifically designed for use in RAPD analysis. The primers are supplied lyophilized and can be reconstituted with 500 µl of sterile distilled water to give a final concentration of 5 pmol\/µl.\u003cbr\u003e\r\n\u003cbr\u003e\r\nReferences\u003cbr\u003e\r\n1. Williams, J. G. et al. Nucl. Acids Res. 18, 6531 (1990). 2. Welsh, J. et al. PCR 2: A Practical Approach, McPherson, M. J., Hames. B. D. and Taylor, G. R., eds., Chapter 11, IRL Press (1995).\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775945986339,"sku":"CYTI27950201","price":2315.1,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27950001.jpg?v=1789943429"},{"product_id":"amersham-ready-to-go-rapd-analysis-beads","title":"Amersham Ready-To-Go RAPD Analysis Beads (100 reactions)","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nRAPD analysis is a technique for rapidly detecting genomic polymorphisms. A single short oligonucleotide primer of arbitrary sequence is used under low stringency conditions in PCR to generate a reproducible array of strain-specific products.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For performing DNA profiling experiments using the randomly amplified polymorphic DNA [RAPD (1)] technique.\u003cbr\u003e\r\n•Preformulated, predispensed, single-dose reaction beads are provided as ambient-temperature-stable beads to ensure greater reproducibility between reactions, minimize pipetting steps and reduce the potential for pipetting errors and contamination.\u003cbr\u003e\r\n•RAPD* reactions are simple to perform—simply add genomic DNA solution and primer to a tube of RAPD Analysis Beads to a final reaction volume of 25 µl and cycle the reaction.\u003cbr\u003e\r\nEach lot of RAPD Analysis Beads is function-tested to ensure its ability to generate a differential banding pattern between the two control E. coli strains using RAPD Analysis Primer 2 included with the RAPD beads.\u003cbr\u003e\r\n•RAPD reactions are pre-optimized for use with a wide variety of organisms.\u003cbr\u003e\r\n\u003cbr\u003e\r\n\u003cbr\u003e\r\nReady-To-Go RAPD Analysis Beads are designed as premixed , predispensed reactions for performing random amplified polymorphic DNA (RAPD) analysis. With RAPD analysis, genomic polymorphisms can be detected at multiple loci using only nanogram quantities of DNA. The RAPD reactions are provided as room-temperature-stable dried beads that contain all the necessary reagents, except primer, for performing RAPD analysis.\u003cbr\u003e\r\n\u003cbr\u003e\r\nRAPD analysis is a technique for rapidly detecting genomic polymorphisms. A single, short oligonucleotide primer of arbitrary sequence is used under low stringency conditions in PCR to generate a reproducible array of strain-specific products that are analyzed by gel electrophoresis. Under these conditions, genomic polymorphisms can be detected at multiple loci using only nanogram quantities of DNA. RAPD analysis has been used in numerous applications, including gene mapping, detection of strain diversity, population analysis, epidemiology and the analysis of phylogenetic and taxonomic relationships (2).\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe RAPD reactions are provided as dried beads that contain all the necessary PCR components, except primer, in concentrations optimized for RAPD analysis. Beads are provided in thin-walled 0.5 ml tubes compatible with most thermal cyclers. Each package of Ready-To-Go RAPD Analysis Beads contains sufficient reagents for 100 individual RAPD reactions: RAPD analysis beads, control E. coli BL21 DNA, control E. coli C1a DNA, RAPD analysis primer 2, and instruction booklet (DNA from two E. coli strains and RAPD analysis primer 2 are provided as controls to assay the ability of the RAPD beads to amplify DNA and identify polymorphisms).\u003cbr\u003e\r\n\u003cbr\u003e\r\nRAPD Analysis Kit consists of Ready-To-Go RAPD Analysis Beads and six primers that can be used with RAPD Analysis Beads. Each primer in the set is an arbitrary 10-mer that is specifically designed for use in RAPD analysis. The primers are supplied lyophilized and can be reconstituted with 500 µl of sterile distilled water to give a final concentration of 5 pmol\/µl.\u003cbr\u003e\r\n\u003cbr\u003e\r\nReferences\u003cbr\u003e\r\n1. Williams, J. G. et al. Nucl. Acids Res. 18, 6531 (1990). 2. Welsh, J. et al. PCR 2: A Practical Approach, McPherson, M. J., Hames. B. D. and Taylor, G. R., eds., Chapter 11, IRL Press (1995).\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775946084643,"sku":"CYTI27950001","price":1382.6,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27950001_bedc01e6-dd79-4b03-a018-da001710b059.jpg?v=1789941016"},{"product_id":"genomiphi-v2-dna-amplification-kit-100-reactions","title":"GenomiPhi V2 DNA amplification kit, 100 reactions","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nGenomiPhi V2 DNA Amplification Kit offers highly efficient and representative whole-genome amplification with 4 to 7 µg yield from nanogram amounts of DNA sample.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Representative isothermal amplification of the whole genome.\u003cbr\u003e\r\n•No template-independent, background amplification product.\u003cbr\u003e\r\n•Outperforms PCR-based whole genome amplification techniques.\u003cbr\u003e\r\n•Quick and simple automation-friendly protocol; no thermal cycler required.\u003cbr\u003e\r\n•Yields high-quality DNA (e.g., for high-throughput genotyping, hybridization, and DNA archival).\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription\u003cbr\u003e\r\nGenomiPhi V2 DNA Amplification Kit is part of the Phi29 DNA polymerase family of products from Cytiva. It contains all of the components necessary for mini-scale whole genome amplification by isothermal strand displacement amplification.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAmplification is highly uniform over the entire genome so that locus representation remains extremely close to the original DNA sample. Furthermore, amplification is carried out with very high fidelity due to Phi29 DNA polymerase proofreading activity.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe GenomiPhi V2 DNA Amplification Kit procedure is quick, simple and does not require a thermocycler. A typical DNA yield of 4 to 7 µg DNA can be achieved in less than two hours with little hands-on time. The average product length is over 10 kb. The starting material for GenomiPhi reactions can be purified DNA from any commercial kit or homebrew method, or a nonpurified cell lysate may be used. The kit was verified with DNA from various clinical samples including FTA card lysates, blood and buccal swabs. GenomiPhi amplified DNA is suitable for various applications such as genotyping (SNP, STR, array CGH), cloning, sequencing, and DNA archival.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775946182947,"sku":"CYTI25660031","price":812.4,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/25660031.jpg?v=1789940734"},{"product_id":"serasil-mag™-700-beads-5-ml","title":"SeraSil-Mag™ 700 beads 5 mL","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nSeraSil-Mag™ silica coated superparamagnetic beads for nucleic acid isolation deliver high purity DNA extraction for highly sensitive applications where sample is scarce. These beads provide an optimal surface for nucleic acid binding with high performance and low background.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•High magnetization (60 emu\/g) and strong binding capacity giving fast magnetic response (~5 secs) and shorten time required for magnetic steps during isolation.\u003cbr\u003e\r\n•Beads come in two sizes (submicroscale diameter 700 nm and 400 nm), offering choice based on surface requirements and high binding capacity due to the small sized particles.\u003cbr\u003e\r\n•Beads are monodispersed with narrow size distribution for consistent, reproducible results.\u003cbr\u003e\r\n•Silanol hydroxyl groups on the bead surface give efficient, high purity isolation of nucleic acids.\u003cbr\u003e\r\n•Tested for microbial contamination.\u003cbr\u003e\r\n•Good buoyancy stability (low sedimentation rate): beads remain well suspended and dispersed for over 90 mins (at 1 mg\/mL concentration),* providing good handling and suitability for automation. *Beads may settle faster at higher concentration.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSeraSil-Mag™ beads are compatible with chaotropic salt chemistry and vortex mixing, roller mixing and sonication.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTightly controlled production processes result in core-shell beads which are uniform and spherical. The silica shell provides a high content of silanol surface groups and encloses the magnetic core. The submicron size allows for a high surface area and abundant binding sites. The narrow particle size distribution assures uniformity and consistency of the beads.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe magnetic nanoparticles within the core provide superparamagnetic properties to the SeraSil-Mag beads, resulting in extremely fast magnetic separation in the presence of a magnet. There is no residual magnetization when the magnetic field is removed, which further contributes to ease of handling during use.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSeraSil-Mag™ beads are supported by Cytiva''s expertise in Sera-Mag™ bead technology and can be customized to your needs at our manufacturing centre of excellence in Cardiff.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is aSample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775946379555,"sku":"CYTI29357373","price":153.7,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29357373.jpg?v=1789946118"},{"product_id":"sephadex-g-100-dna-grade-sf-100-g","title":"Sephadex G-100 DNA Grade SF, 100g","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nSephadex™ G-100 DNA Grade is ideal for use in preparing spin columns for DNA purification.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For DNA purification from small molecules by gel filtration in spin columns with an exclusion limit of 25bp ds DNA\u003cbr\u003e\r\n•Tested to ensure reproducibly high recovery of DNA\u003cbr\u003e\r\n•Suitable for researchers who prefer to prepare their own columns for nucleic acid purification\u003cbr\u003e\r\n•Sephadex G-50 DNA Grade is used in AutoSeq G-50 columns, ProbeQuant G-50 Micro Columns, MicroSpin G-50 Columns, and NICK Columns\u003cbr\u003e\r\n\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-100 is one of five different G-types ranging from G-10 for small molecules to G-75 for larger molecules. Spin columns packed with Sephadex G-100 DNA Grade allow for high-recovery nucleic acid purification via gel filtration. Gel filtration resins do not exhibit a fixed exclusion limit when used in a spin-column format. In spin-column chromatography, the observed exclusion properties that allow the product to pass through the gel while the smaller impurities are retained depend on experimental factors, such as the resin used, sample volume, product size, and the g-forces used in the purification process.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-50 is a well-established gel filtration resin for desalting and buffer exchange of biomolecules \u0026gt;30 000 molecular weight, and with a spin protocol can be used for DNA and oligo purification of molecules greater than 20 bases in length. Sephadex G-25 has an exclusion limit of approximately Mr 5000, and when packed into empty MicroSpin columns, the resulting desalting columns can be used in a spin protocol for DNA and oligo purification of any DNA greater than 10 bases in length.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAll these Sephadex types are therefore highly suitable for the purification of oligonucleotides or small DNA fragments following synthesis or in labeling applications.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-50 DNA Grade, and Sephadex G-25 are also sold separately.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775946576163,"sku":"CYTI17057402","price":685.0,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/17057402.jpg?v=1789940116"},{"product_id":"amersham-hot-start-mix-ready-to-go-480-reactions","title":"Amersham Hot Start Mix Ready-To-Go, 480 reactions","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nPreformulated and predispensed, freeze-dried PCR reagents mix including high-quality PuReTaq DNA Polymerase and a hot start activator protein, for increased specificity and reproducibility of PCR amplifications.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Recombinant hot start activator protein sequesters primers prior to PCR, effectively reducing nonspecific priming and primer-dimer formation.\u003cbr\u003e\r\n•Avoids the risk of contamination from a mammalian source associated with hot start antibodies.\u003cbr\u003e\r\n•Quick hot start activation preserves sample integrity by avoiding extensive precycling heat treatment.\u003cbr\u003e\r\n•Streamlines the workflow and yields more reproducible results.\u003cbr\u003e\r\n•Long-term ambient-temperature stable: no freezer space required; less energy consumption for shipping and storage\u003cbr\u003e\r\n•Validated for real-time PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription:\u003cbr\u003e\r\nHot Start Mix RTG is a premixed, predispensed, ambient temperature- stable formulation that can effectively reduce nonspecific priming and primer-dimer formation during PCR. The system is based on a novel hot start method that uses a hot start activator protein to sequester primers prior to PCR, thereby making them unavailable for nonspecific priming during the reaction preparation. This method requires only a quick 2 min initial PCR activation step. In contrast, other commercially available hot start PCR kits that are based on chemical inactivation require prolonged incubation at high temperatures, which may damage the DNA template by heat-induced depurination. The net result from using Hot Start Mix RTG is a more robust and reliable amplification of the target amplicons with increased yield when compared with conventional hot start master mix products. Furthermore, the mix does not contain Taq antibody and this eliminates the risk of mammalian-source contamination.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThis Ready-To-Go format provides reproducible and reliable performance for demanding PCR applications in which high specificity and high sensitivity are essential to success.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775946674467,"sku":"CYTI28900654","price":1425.9,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/28900654.jpg?v=1789944316"},{"product_id":"genomiphi-v3-ready-to-go-dna-amplification-kit-480-reactions","title":"GenomiPhi V3 Ready-To-Go DNA amplification kit, 480 reactions","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nGenomiPhi V3 Ready-To-Go DNA Amplification Kit offers highly efficient and representative whole-genome amplification with 12 to 20 µg yield from nanogram amounts of DNA sample.\u003cbr\u003e\r\n\u003cbr\u003e\r\nRepresentative amplification of the whole genome.\u003cbr\u003e\r\n•Preformulated, predispensed, single-dose, lyophilized cakes for rapid reaction set-up and greater reproducibility.\u003cbr\u003e\r\n•Quick and simple automation-friendly protocol; no thermal cycler required.\u003cbr\u003e\r\n•Shipping and storage at room temperature provides easy access and reduced carbon footprint.\u003cbr\u003e\r\n•Yields high-quality DNA (e.g. for high-throughput genotyping and DNA archival).\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription:\u003cbr\u003e\r\nGenomiPhi V3 Ready-To-Go DNA Amplification Kit is part of the Phi29 DNA polymerase family of products from Cytiva. It contains all of the components necessary for whole genome amplification by isothermal strand displacement amplification. The reaction mixture is provided as predispensed, single-dose, lyophilized cakes in either strips of 8 tubes, or 96-well plates.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAmplification is highly uniform over the entire genome so that locus representation remains extremely close to the original DNA sample. Furthermore, amplification is carried out with very high fidelity due to Phi29 DNA polymerase proofreading activity. The average product length is over 10 kb.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe GenomiPhi V3 Ready-To-Go DNA Amplification Kit procedure is quick, simple and does not require a thermocycler. A typical DNA yield of 12 to 20 µg DNA can be achieved in less than two hours from only 10 ng of genomic DNA input. The starting material for GenomiPhi reactions can be purified DNA from any commercial kit or homebrew method, or a nonpurified cell lysate may be used. Protocols for the amplification of DNA from blood lysates and dried blood spots are included in the manual.\u003cbr\u003e\r\n\u003cbr\u003e\r\nGenomiPhi amplified DNA is suitable for various applications such as genotyping (SNP, STR, array CGH), cloning, sequencing, and DNA archival.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775946772771,"sku":"CYTI29013588","price":3993.1,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29013586.jpg?v=1789945517"},{"product_id":"puretaq-ready-to-go-pcr-beads-0-5-ml-tubes-100-reactions","title":"PuReTaq Ready-To-Go PCR beads (0.5ml tubes), 100 reactions","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nPuReTaq RTG PCR beads and reagents ensures reliable and robust performance in both end point and RT-PCR amplifications and ensures the lowest possible levels of contaminating prokaryotic and eukaryotic nucleic acids.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Save time by simply adding template DNA solution and primers, then cycle\u003cbr\u003e\r\n•More reproducible results, less risk of pipetting errors and contamination\u003cbr\u003e\r\n•High-quality PuReTaq DNA polymerase and high-purity reagents ensure robust performance and the lowest possible levels of contaminating DNA\u003cbr\u003e\r\n•Long-term ambient-temperature stable at room temperature PCR reaction mixes means no freezer space is required and less energy consumption for shipping and storage\u003cbr\u003e\r\n•Verified for real-time PCR (RT-PCR)\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe PuReTaq Ready-To-Go PCR Beads are pre-formulated to ensure greater reproducibility between reactions.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe only additional reagents required are water, primers, and template DNA. The beads are provided pre-dispensed into either 0.2 mL or 0.5 mL PCR tubes. The 0.2 mL tubes are also supplied in a 96-well (8 × 12) plate format that allows individual strips of eight tubes to be easily removed. This flexibility allows use of either the entire 96-well plate, strips of eight, or individual 0.2 mL tubes.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775946871075,"sku":"CYTI27955801","price":255.8,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27955901.jpg?v=1789943432"},{"product_id":"sera-mag-oligo-dt-coated-magnetic-particles-100-ml","title":"Sera-Mag Oligo (dT) Coated Magnetic particles, 100ml","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nSera-Mag Oligo(dT)-Coated Magnetic Particles enable mRNA isolation and extraction for applications such as RT-PCR, cDNA library construction, cDNA microarrays, affinity purification, primer extension, and subtractive hybridization.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Encapsulation means no exposed iron and minimized interference with downstream enzymatic applications\u003cbr\u003e\r\n•Covalently bound oligo(dT)14 prevents leaching from the particle surface\u003cbr\u003e\r\n•Very high, specific poly A+ binding capacity ensures maximum extraction of mRNA\u003cbr\u003e\r\n•Fast reaction kinetics increase throughput and precision, also enabling faster movement through viscous solutions\u003cbr\u003e\r\n•Uniform, nominal 1 µm diameter provides high surface area and excellent lot-to-lot reproducibility\u003cbr\u003e\r\n•Also available as custom-manufactured magnetic beads\u003cbr\u003e\r\n\u003cbr\u003e\r\nConvenient and efficient mRNA isolation:\u003cbr\u003e\r\nEukaryotic mRNA makes up only 1 to 3% of total cellular RNA, so efficient mRNA purification is critical. Sera-Mag Oligo(dT) Magnetic Particles remove 90% or more of mRNA from total RNA with just one extraction. Sera-Mag Oligo(dT) Magnetic Particles bind target mRNA through pairing of the polyadenylated RNA tail found on the 3’ end of mRNA to the covalently bound oligo(dT) groups on the surface of the particles. This binding is easily accomplished using standard hybridization conditions during the mRNA purification process.\u003cbr\u003e\r\n\u003cbr\u003e\r\nFast magnetic response times and stable physical integrity:\u003cbr\u003e\r\nThe core of the particle is made by a free radical emulsion polymerization of styrene and acid monomer. One layer of magnetite is coated onto this core, while the surface is modified to minimize non-specific binding of proteins. Oligo(dT) groups are then covalently bound to the particle surface. Since the magnetite is encapsulated, there is no exposed iron minimizing interference with downstream enzymatic applications.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775946969379,"sku":"CYTI29103134","price":5360.3,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29103135.jpg?v=1789945820"},{"product_id":"thermo-sequenase-dna-polymerase-with-thermoplasma-acidophilum-inorganic-pyrophosphatase-tap","title":"Thermo Sequenase DNA Polymerase (with Thermoplasma acidophilum Inorganic Pyrophosphatase (TAP))","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nThermo Sequenase™ DNA polymerase is a novel thermostable DNA polymerase that uses ddNTPs as readily as dNTP substrates at temperatures similar to those used in standard PCR. The result is:\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Uniform and easy-to-read band patterns\u003cbr\u003e\r\n•Better incorporation of ddNTPs helps avoid secondary structures that can cause unreadable sequences\u003cbr\u003e\r\n•Read-through of difficult sequences (e.g., GC-rich), due to the ability of thermostable enzymes to function at elevated temperature used for sequencing\u003cbr\u003e\r\n\u003cbr\u003e\r\nddNTPs are chain-elongating inhibitors of DNA polymerase, which are used in the Sanger method for DNA sequencing. Each nucleotide base of that particular type has a probability of being bonded not to a deoxynucleotide but rather a dideoxynucleotide, which ends chain elongation. This property, in addition to thermostability, makes Thermo Sequenase™ DNA polymerase an excellent choice for cycle sequencing where template quantity limitations preclude the use of T7 Sequenase DNA polymerase.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe properties of Thermo Sequenase™ also enable its use in many SNP genotyping, genotyping by sequencing, or genome sequencing applications where primer extension is employed.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947067683,"sku":"CYTI25003963","price":8850.0,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/25003962.jpg?v=1789940421"},{"product_id":"amersham-shrimp-alkaline-phosphatase-500","title":"Amersham Shrimp Alkaline Phosphatase, 500 Units","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nAlkaline phosphatase is suitable for dephosphorylation of 5'' and 3''-overhangs, recessed ends, blunt ends, and single nucleotides. Following incubation, alkaline phosphatase can be easily inactivated by heating.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Bacterial alkaline phosphatase recombinantly expressed in E. coli.\u003cbr\u003e\r\n•Active in PCR and restriction endonuclease buffers.\u003cbr\u003e\r\n•Inactivated by heating at 75°C for 5 minutes.\u003cbr\u003e\r\n\u003cbr\u003e\r\nUse together with Exonuclease I for cleaning up PCR reactions prior to downstream application such as DNA sequencing.\u003cbr\u003e\r\n\u003cbr\u003e\r\nUnit Definition\u003cbr\u003e\r\nOne unit is the amount of the enzyme required to dephosphorylate 1 µg of linearized pUC57 DNA termini in 10 minutes at 37°C.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is a Sample Only*\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947133219,"sku":"CYTI25003934","price":156.2,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/25003935.jpg?v=1789940423"},{"product_id":"taq-dna-polymerase-cloned-10-x-250-units","title":"Taq DNA Polymerase (cloned), 10 x 250 Units","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nTaq DNA Polymerase is a single subunit enzyme purified from the thermophilic bacterium Thermus aquaticus, the native enzyme expressed in E. coli. It polymerizes DNA from a primer annealed to a DNA template in the presence of dNTP for PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Highly purified recombinant enzyme.\u003cbr\u003e\r\n•Excellent batch-to-batch reproducibility.\u003cbr\u003e\r\n•Each lot is tested to be free of nuclease contamination.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTaq DNA Polymerase (cloned) is the recombinant (segments of DNA from different sources joined together) form of the native enzyme, expressed in E. coli. This serves as a source of energy for cellular reactions and is involved in signaling pathways.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAs Taq DNA Polymerase (cloned) is an exceptionally pure recombinant protein, it provides excellent batch-to-batch reproducibility, at an optimum temperature of 75°C, with the ability to survive repeated incubations at \u0026gt; 95°C.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTaq DNA Polymerase is licensed for use in PCR and is extensively tested for contaminating nickase, single- and double-stranded exonuclease, and endonuclease activities.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947231523,"sku":"CYTI27079806","price":1108.8,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27079806.jpg?v=1789940736"},{"product_id":"amersham-nap-10-columns","title":"Amersham NAP-10 Columns","description":"\u003cp\u003eNAP DNA columns are disposable DNA purification size exclusion columns, prepacked with Sephadex G-25 DNA Grade which require only gravity to run.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For rapid and efficient purification of DNA and oligonucleotides (= 10-mers) in less than 15 minutes by gravity flow\u003cbr\u003e\r\n•Prepacked with Sephadex G-25 DNA Grade in distilled water containing 0.15% Kathon CG\/ICP Biocide\u003cbr\u003e\r\n•Available in three sizes depending on sample volume: 0.5 mL (NAP-5), 1 mL (NAP-10) or 2.5 mL (NAP-25)\u003cbr\u003e\r\n•Useful for small-scale purification, oligo purification, desalting, and buffer exchange\u003cbr\u003e\r\n\u003cbr\u003e\r\nNAP DNA purification columns with Sephadex G-25 DNA Grade can be used for any DNA greater than 10 bases in length. These disposable DNA purification columns are ideal for the purification of oligonucleotides or very small DNA fragments following synthesis or a DNA labeling reaction, and for downstream applications such as PCR amplification and sequencing.\u003cbr\u003e\r\n\u003cbr\u003e\r\nEach package includes a complete step-by-step protocol describing the fixed volumes needed for equilibration, washing, and sample elution.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-25 is one of five different G-types ranging from G-10 for small molecules to G-75 for larger molecules. Sephadex G-25 has an exclusion limit of approximately Mr 5000, and when packed into empty MicroSpin columns, the resulting desalting columns can be used in a spin protocol for DNA and oligo purification of any DNA greater than 10 bases in length.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947329827,"sku":"CYTI17085401","price":309.1,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/17085201.jpg?v=1789940426"},{"product_id":"nucleon-phytopure-1-0-g-50-preps-x-1-0-g","title":"Nucleon PhytoPure 1.0 g, 50 preps x 1.0 g (RPN8511)","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nNucleon PhytoPure produces the DNA quality, length, and purity of a phenol-chloroform extraction without phenol.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Efficiently removes plant polysaccharides ensuring high yields of high-quality plant genomic DNA in only 1 h\u003cbr\u003e\r\n•Two kit sizes provide economical scale-up using the same phenol-free protocol\u003cbr\u003e\r\n\u003cbr\u003e\r\nNucleon PhytoPure, a DNA extraction kit for high-quality plant and fungal genomic DNA purification\u003cbr\u003e\r\n\u003cbr\u003e\r\nNucleon PhytoPure extracts genomic DNA from plant and fungal samples in a fraction of the time taken by conventional methods, while efficiently removing proteins and polysaccharides. Polysaccharides are very common contaminants in plant DNA extracts, and often result in difficult-to-handle, \"slimy\" DNA pellets. Although most plant DNA extraction techniques are effective at removing proteins, they are much less successful with polysaccharides.\u003cbr\u003e\r\n\u003cbr\u003e\r\nNucleon PhytoPure proprietary resin is added following cell lysis with Potassium SDS, and a single chloroform extraction. Aspiration of the top layer of nucleic acids is simplified and the volume of usable sample maximized by a barrier formed between the two layers. The combination of purity and high molecular weight makes the recovered DNA suitable in multiple downstream molecular biology applications, including whole genome amplification (WGA) for applications such as next generation sequencing.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947428131,"sku":"CYTI25006721","price":735.6,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/25006720.jpg?v=1789940429"},{"product_id":"genomiphi-v2-dna-amplification-kit-25-reactions","title":"GenomiPhi V2 DNA amplification kit, 25 reactions","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nGenomiPhi V2 DNA Amplification Kit offers highly efficient and representative whole-genome amplification with 4 to 7 µg yield from nanogram amounts of DNA sample.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Representative isothermal amplification of the whole genome.\u003cbr\u003e\r\n•No template-independent, background amplification product.\u003cbr\u003e\r\n•Outperforms PCR-based whole genome amplification techniques.\u003cbr\u003e\r\n•Quick and simple automation-friendly protocol; no thermal cycler required.\u003cbr\u003e\r\n•Yields high-quality DNA (e.g., for high-throughput genotyping, hybridization, and DNA archival).\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription\u003cbr\u003e\r\nGenomiPhi V2 DNA Amplification Kit is part of the Phi29 DNA polymerase family of products from Cytiva. It contains all of the components necessary for mini-scale whole genome amplification by isothermal strand displacement amplification.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAmplification is highly uniform over the entire genome so that locus representation remains extremely close to the original DNA sample. Furthermore, amplification is carried out with very high fidelity due to Phi29 DNA polymerase proofreading activity.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe GenomiPhi V2 DNA Amplification Kit procedure is quick, simple and does not require a thermocycler. A typical DNA yield of 4 to 7 µg DNA can be achieved in less than two hours with little hands-on time. The average product length is over 10 kb. The starting material for GenomiPhi reactions can be purified DNA from any commercial kit or homebrew method, or a nonpurified cell lysate may be used. The kit was verified with DNA from various clinical samples including FTA card lysates, blood and buccal swabs. GenomiPhi amplified DNA is suitable for various applications such as genotyping (SNP, STR, array CGH), cloning, sequencing, and DNA archival.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947493667,"sku":"CYTI25660030","price":292.8,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/25660031_b9ead3af-013c-4101-b124-3a6c1e3f5be0.jpg?v=1789940739"},{"product_id":"autoseq-g-50-50-columns","title":"AutoSeq G-50, 50 columns","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nAutoSeq G-50 columns are specifically designed to remove fluorescent dye-terminators from cycle sequencing reactions prior to analysis on automated sequencers.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For rapid removal of unincorporated fluorescent dye-terminators from cycle sequencing reactions prior to automated DNA sequencing\u003cbr\u003e\r\n•Columns are prepacked with Sephadex G-50 DNA Grade F\u003cbr\u003e\r\n•Columns are pre-equilibrated in double-distilled water with 0.05% Kathon CG\/ICP Biocide added as a preservative\u003cbr\u003e\r\n•Ready-to-use columns enable sample application through to collection of purified product in less than 4 min\u003cbr\u003e\r\n•4 minutes\u003cbr\u003e\r\n\u003cbr\u003e\r\nEffective DNA purification is essential for high-quality results on automated DNA sequencing since residual dye-terminators can obscure data.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAutoSeq G-50 consists of MicroSpin columns containing Sephadex G-50 DNA Grade F, pre-equilibrated in double-distilled water. This is important because even the small amount of salt in traditional buffers (such as TE buffer) can cause electrophoretic artefacts on salt-sensitive automated DNA sequencers.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is a Sample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947755811,"sku":"CYTI27534001","price":277.5,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27534003_61cd0ee3-c635-46ac-a59e-29443b1abd23.jpg?v=1789940742"},{"product_id":"serasil-mag™-700-beads-60-ml","title":"SeraSil-Mag™ 700 beads 60ml","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nSeraSil-Mag™ silica coated superparamagnetic beads for nucleic acid isolation deliver high purity DNA extraction for highly sensitive applications where sample is scarce. These beads provide an optimal surface for nucleic acid binding with high performance and low background.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•High magnetization (60 emu\/g) and strong binding capacity giving fast magnetic response (~5 secs) and shorten time required for magnetic steps during isolation.\u003cbr\u003e\r\n•Beads come in two sizes (submicroscale diameter 700 nm and 400 nm), offering choice based on surface requirements and high binding capacity due to the small sized particles.\u003cbr\u003e\r\n•Beads are monodispersed with narrow size distribution for consistent, reproducible results.\u003cbr\u003e\r\n•Silanol hydroxyl groups on the bead surface give efficient, high purity isolation of nucleic acids.\u003cbr\u003e\r\n•Tested for microbial contamination.\u003cbr\u003e\r\n•Good buoyancy stability (low sedimentation rate): beads remain well suspended and dispersed for over 90 mins (at 1 mg\/mL concentration),* providing good handling and suitability for automation. *Beads may settle faster at higher concentration.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSeraSil-Mag™ beads are compatible with chaotropic salt chemistry and vortex mixing, roller mixing and sonication.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTightly controlled production processes result in core-shell beads which are uniform and spherical. The silica shell provides a high content of silanol surface groups and encloses the magnetic core. The submicron size allows for a high surface area and abundant binding sites. The narrow particle size distribution assures uniformity and consistency of the beads.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe magnetic nanoparticles within the core provide superparamagnetic properties to the SeraSil-Mag beads, resulting in extremely fast magnetic separation in the presence of a magnet. There is no residual magnetization when the magnetic field is removed, which further contributes to ease of handling during use.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSeraSil-Mag™ beads are supported by Cytiva''s expertise in Sera-Mag™ bead technology and can be customized to your needs at our manufacturing centre of excellence in Cardiff.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is aSample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947821347,"sku":"CYTI29357374","price":741.9,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29357374.jpg?v=1789946121"},{"product_id":"exonuclease-i-5000-units","title":"E70073X Exonuclease I, 5000 Units","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nExonuclease I is used to selectively digest excess single stranded DNA in a mixture also containing double-stranded DNA, such as removing unused primers after PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•3''-5'' single-stranded exonuclease.\u003cbr\u003e\r\n•Monomeric 54.5 kDa bacterial exonuclease I recombinantly expressed in E. coli.\u003cbr\u003e\r\n•Inactivated by heating at 80°C for 15 minutes.\u003cbr\u003e\r\n•Active in PCR buffers.\u003cbr\u003e\r\n\u003cbr\u003e\r\nExonuclease I, used together with Alkaline Phosphatase for inactivation of dNTPs, provides effective cleanup of PCR reactions for subsequent use in DNA sequencing.\u003cbr\u003e\r\n\u003cbr\u003e\r\nDigestion of single stranded DNA by Exonuclease I releases dNTPs leaving 5''-terminal dinucleotides intact. DNA strands with terminal 3''-OH groups blocked by phosphoryl or acetyl groups are not removed.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947886883,"sku":"CYTI27700734","price":480.8,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27700734_f137f08e-ddb3-4742-85c2-5ba8b6f64dbd.jpg?v=1789940745"},{"product_id":"genomiphi-v3-ready-to-go-dna-amplification-kit-96-reactions-1","title":"GenomiPhi V3 Ready-To-Go DNA amplification kit, 96 reactions","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nGenomiPhi V3 Ready-To-Go DNA Amplification Kit offers highly efficient and representative whole-genome amplification with 12 to 20 µg yield from nanogram amounts of DNA sample.\u003cbr\u003e\r\n\u003cbr\u003e\r\nRepresentative amplification of the whole genome.\u003cbr\u003e\r\n•Preformulated, predispensed, single-dose, lyophilized cakes for rapid reaction set-up and greater reproducibility.\u003cbr\u003e\r\n•Quick and simple automation-friendly protocol; no thermal cycler required.\u003cbr\u003e\r\n•Shipping and storage at room temperature provides easy access and reduced carbon footprint.\u003cbr\u003e\r\n•Yields high-quality DNA (e.g. for high-throughput genotyping and DNA archival).\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription:\u003cbr\u003e\r\nGenomiPhi V3 Ready-To-Go DNA Amplification Kit is part of the Phi29 DNA polymerase family of products from Cytiva. It contains all of the components necessary for whole genome amplification by isothermal strand displacement amplification. The reaction mixture is provided as predispensed, single-dose, lyophilized cakes in either strips of 8 tubes, or 96-well plates.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAmplification is highly uniform over the entire genome so that locus representation remains extremely close to the original DNA sample. Furthermore, amplification is carried out with very high fidelity due to Phi29 DNA polymerase proofreading activity. The average product length is over 10 kb.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe GenomiPhi V3 Ready-To-Go DNA Amplification Kit procedure is quick, simple and does not require a thermocycler. A typical DNA yield of 12 to 20 µg DNA can be achieved in less than two hours from only 10 ng of genomic DNA input. The starting material for GenomiPhi reactions can be purified DNA from any commercial kit or homebrew method, or a nonpurified cell lysate may be used. Protocols for the amplification of DNA from blood lysates and dried blood spots are included in the manual.\u003cbr\u003e\r\n\u003cbr\u003e\r\nGenomiPhi amplified DNA is suitable for various applications such as genotyping (SNP, STR, array CGH), cloning, sequencing, and DNA archival.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775947952419,"sku":"CYTI29013587","price":844.0,"currency_code":"NZD","in_stock":true}]},{"product_id":"sera-xtracta-cell-free-dna-kit","title":"Sera-Xtracta Cell-Free DNA Kit","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nDesigned to select for small-fragment cfDNA while minimizing genomic DNA contamination, Sera-Xtracta™ Cell-Free DNA Kit* offers reliable extraction and purification of cfDNA for liquid biopsy from samples including plasma, serum and urine. High yield and sensitivity make the kit well-suited for applications such as cancer diagnosis and monitoring, even when sample is limited.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Efficient recovery of small-fragment cfDNA in the size range 50-300 bp: capture more cfDNA to increase sensitivity levels.\u003cbr\u003e\r\n•Minimal co-purification of higher molecular weight genomic DNA due to active selection of smaller fragments which improves sensitivity in downstream applications.\u003cbr\u003e\r\n•Scalability: one kit to cover up to 4 mL input of sample.\u003cbr\u003e\r\n•Efficient extraction: procedure can be completed in 120 minutes.\u003cbr\u003e\r\n•Ease of use: compatible with molecular biology techniques, including next-generation sequencing (NGS), qPCR, ddPCR, BEAMing and other amplification and genotyping applications.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe method uses chaotropic agents and detergents to disrupt protein components to which the cfDNA may initilally bind and to promote the selective binding of this cfDNA to the silica magnetic beads.\u003cbr\u003e\r\n\u003cbr\u003e\r\nProteinase K is used to digest protein from samples; denatured contaminants are easily removed by subsequent washing of the silica beads with specially formulated wash buffers. Proteinase K treatment is also required to release the cfDNA from plasma derived from blood collected in tubes with cfDNA stabilization, such as Cell Free DNA BCT™ (Streck™) for reversal of the stabilization\/release of cfDNA.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe purified cfDNA is eluted in a low ionic strength buffer, at a concentration suitable for most downstream molecular biology applications, such as next-generation sequencing (NGS). Automation scripts available, please contact Scientific Support.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is a Sample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775948017955,"sku":"CYTI29437807","price":1547.9,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29437807.jpg?v=1789941018"},{"product_id":"blood-genomicprep-mini-spin-kit-250-pkg","title":"Blood genomicPrep Mini Spin Kit","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nBlood genomicPrep Mini Spin Kit is designed for the rapid extraction and purification of high molecular weight genomic DNA (gDNA) from whole blood, buffy coat, bone marrow, and nucleated red blood cells.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•High-quality genomic DNA extraction from blood with a greater proportion of higher molecular weight DNA and less shearing\u003cbr\u003e\r\n•Demonstrated application to various types of whole blood including human, horse, rabbit, rat, and mouse\u003cbr\u003e\r\n•Increased ease of use with reduced pipetting volume changes, one centrifugation setting, and color-coded kit components\u003cbr\u003e\r\n•Verified in several downstream applications including reverse transcription polymerase chain reaction (RT-PCR), endpoint PCR, multiplex PCR, and restriction enzyme digests\u003cbr\u003e\r\n\u003cbr\u003e\r\n\u003cbr\u003e\r\nGenomic DNA is found in the chromosomes and it is much longer and higher in molecular weight than plasmid DNA. Genomic DNA is the code for the genome, and this is what is needed to do genome sequencing.\u003cbr\u003e\r\n\u003cbr\u003e\r\nFor sequencing it is desirable that the genomic DNA extraction technique used allows the collection of intact genomic DNA in the longest fragments possible. A kit format can help standardize the procedures used to prepare tissue and cell genomic DNA samples for analysis.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe purification process involves minimal shearing resulting in the production of 5 to 10 µg of good quality, intact genomic DNA from a 200 µL sample. Input sample volumes can vary from 50 µL to 1 mL.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe method uses a simple genomic DNA purification protocol. This protcol that uses chaotropic agents to extract DNA from blood cells, denature protein components, and promote the selective binding of DNA to a column-based, novel silica membrane. This results in high molecular weight DNA that can be used downstream (e.g., in bone marrow genomic DNA for next generation sequencing).\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe elution volume can be modified as necessary to obtain the appropriate genomic DNA concentration for most downstream molecular biological applications.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe genomic DNA kit contains spin columns prepacked with a novel silica membrane, lyophilized proteinase K powder, lysis solution, wash and elution buffers, microcentrifuge collection tubes, a full protocol booklet, and a detachable, quick reference protocol card.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775948214563,"sku":"CYTI28904265","price":1427.8,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/28904264.jpg?v=1789944917"},{"product_id":"amersham-nap-10-columns-1","title":"Amersham NAP-10 Columns","description":"\u003cp\u003eNAP DNA columns are disposable DNA purification size exclusion columns, prepacked with Sephadex G-25 DNA Grade which require only gravity to run.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For rapid and efficient purification of DNA and oligonucleotides (= 10-mers) in less than 15 minutes by gravity flow\u003cbr\u003e\r\n•Prepacked with Sephadex G-25 DNA Grade in distilled water containing 0.15% Kathon CG\/ICP Biocide\u003cbr\u003e\r\n•Available in three sizes depending on sample volume: 0.5 mL (NAP-5), 1 mL (NAP-10) or 2.5 mL (NAP-25)\u003cbr\u003e\r\n•Useful for small-scale purification, oligo purification, desalting, and buffer exchange\u003cbr\u003e\r\n\u003cbr\u003e\r\nNAP DNA purification columns with Sephadex G-25 DNA Grade can be used for any DNA greater than 10 bases in length. These disposable DNA purification columns are ideal for the purification of oligonucleotides or very small DNA fragments following synthesis or a DNA labeling reaction, and for downstream applications such as PCR amplification and sequencing.\u003cbr\u003e\r\n\u003cbr\u003e\r\nEach package includes a complete step-by-step protocol describing the fixed volumes needed for equilibration, washing, and sample elution.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-25 is one of five different G-types ranging from G-10 for small molecules to G-75 for larger molecules. Sephadex G-25 has an exclusion limit of approximately Mr 5000, and when packed into empty MicroSpin columns, the resulting desalting columns can be used in a spin protocol for DNA and oligo purification of any DNA greater than 10 bases in length.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is a Sample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775948312867,"sku":"CYTI17085402","price":606.4,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/17085201_4d716f81-a5b5-4405-ab41-7fc97c4f9392.jpg?v=1789940432"},{"product_id":"taq-dna-polymerase-cloned-250-units","title":"Taq DNA Polymerase (cloned), 250 Units","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nTaq DNA Polymerase is a single subunit enzyme purified from the thermophilic bacterium Thermus aquaticus, the native enzyme expressed in E. coli. It polymerizes DNA from a primer annealed to a DNA template in the presence of dNTP for PCR.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Highly purified recombinant enzyme.\u003cbr\u003e\r\n•Excellent batch-to-batch reproducibility.\u003cbr\u003e\r\n•Each lot is tested to be free of nuclease contamination.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTaq DNA Polymerase (cloned) is the recombinant (segments of DNA from different sources joined together) form of the native enzyme, expressed in E. coli. This serves as a source of energy for cellular reactions and is involved in signaling pathways.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAs Taq DNA Polymerase (cloned) is an exceptionally pure recombinant protein, it provides excellent batch-to-batch reproducibility, at an optimum temperature of 75°C, with the ability to survive repeated incubations at \u0026gt; 95°C.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTaq DNA Polymerase is licensed for use in PCR and is extensively tested for contaminating nickase, single- and double-stranded exonuclease, and endonuclease activities.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775948575011,"sku":"CYTI27079804","price":170.2,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27079806_68fecd57-95b7-492a-800e-f04960b2d041.jpg?v=1789940748"},{"product_id":"amersham-microspin-g-25-columns","title":"Amersham MicroSpin G-25 Columns","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nMicroSpin G-25 columns are designed for the rapid purification of DNA for use in a wide range of applications, including desalting, buffer exchange, and removal of unincorporated nucleotides from end-labeled oligonucleotides.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Excellent for rapid buffer exchange\/desalting: for example, of PCR amplification products and other DNAs in a volume of 10 to 100 µL using spin-column chromatography\u003cbr\u003e\r\n•Excellent for rapid DNA purification: especially newly synthesized oligonucleotides \u0026gt; 10-mers in 100 to 150 µL of deprotection solution\u003cbr\u003e\r\n•Convenient: Prepacked with Sephadex G-25 DNA Grade and pre-equilibrated in distilled wa-ter containing 0.05% Kathon CG\/ICP Biocide\u003cbr\u003e\r\n•Ready to use: requires less than 4 minutes from sample application to collection of purified oligonucleotides\u003cbr\u003e\r\n•Tested in assays: including nickase, single- and double-stranded exonuclease, and RNase\u003cbr\u003e\r\n•Use additionally: for desalting\/buffer exchange of DNA and removal of unincorporated radi-onucleotides from end-labeled oligonucleotides (at least 10 bases in length) in a volume of 10 to 100 µL\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin G-25 columns for rapid DNA purification in desalting and buffer exchange applications\u003cbr\u003e\r\nMicroSpin G-25 columns are appropriate for use with DNA greater than 10 bases in length and are therefore an excellent choice for the purification of oligonucleotides or very small DNA fragments following synthesis or labeling reactions. They will not remove or denature enzymes.\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin G-25 columns contain Sephadex G-25 DNA Grade F resin. They allow DNA purification via gel filtration. Gel filtration resins do not exhibit a fixed exclusion limit when used in a spin-column format. In spin-column chromatography, the observed exclusion properties that allow the product to pass through the gel while the smaller impurities are retained depends on experimental factors. These factors include the resin used, sample volume, product size, and the g-forces used.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe resin used in these columns, Sephadex G-25 has an exclusion limit of approximately Mr 5000. With a spin protocol this resin can be used for any DNA greater than 10 bases in length.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-25 is one of five different G-types ranging from G-10 for small molecules to G-100 for larger molecules. Sephadex G-50 is a well-established gel filtration resin for desalting and buffer exchange of biomolecules \u0026gt;30 000 molecular weight, and with a spin protocol can be used for DNA and oligo purification of molecules greater than 20 bases in length. Sephadex G-100 DNA Grade has an exclusion limit of 25bp ds DNA.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAll these Sephadex types are therefore highly suitable for the purification of oligonucleotides or small DNA fragments following synthesis or labeling reactions.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-25, G-50 DNA Grade and Sephadex G-100 are all sold separately.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775948673315,"sku":"CYTI27532501","price":368.7,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27532501.jpg?v=1789940751"},{"product_id":"puretaq-ready-to-go-pcr-beads-multiwell-plate-5-x-96-reactions","title":"PuReTaq Ready-To-Go PCR beads (multiwell plate), 5 x 96 reactions","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nPuReTaq RTG PCR beads and reagents ensures reliable and robust performance in both end point and RT-PCR amplifications and ensures the lowest possible levels of contaminating prokaryotic and eukaryotic nucleic acids.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Save time by simply adding template DNA solution and primers, then cycle\u003cbr\u003e\r\n•More reproducible results, less risk of pipetting errors and contamination\u003cbr\u003e\r\n•High-quality PuReTaq DNA polymerase and high-purity reagents ensure robust performance and the lowest possible levels of contaminating DNA\u003cbr\u003e\r\n•Long-term ambient-temperature stable at room temperature PCR reaction mixes means no freezer space is required and less energy consumption for shipping and storage\u003cbr\u003e\r\n•Verified for real-time PCR (RT-PCR)\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe PuReTaq Ready-To-Go PCR Beads are pre-formulated to ensure greater reproducibility between reactions.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe only additional reagents required are water, primers, and template DNA. The beads are provided pre-dispensed into either 0.2 mL or 0.5 mL PCR tubes. The 0.2 mL tubes are also supplied in a 96-well (8 × 12) plate format that allows individual strips of eight tubes to be easily removed. This flexibility allows use of either the entire 96-well plate, strips of eight, or individual 0.2 mL tubes.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775948771619,"sku":"CYTI27955702","price":1134.1,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27955901_ccfbe065-b440-4f90-b0d3-61240d8c299e.jpg?v=1789943435"},{"product_id":"genomiphi-hy-dna-amplification-kit-100-reactions","title":"GenomiPhi HY DNA amplification kit, 100 reactions","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nGenomiPhi HY DNA Amplification Kit offers highly efficient and representative whole-genome amplification with 40 to 50 µg yield from nanogram amounts of DNA sample.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Representative isothermal amplification of the whole genome.\u003cbr\u003e\r\n•No template-independent, background amplification product.\u003cbr\u003e\r\n•Outperforms PCR-based whole genome amplification techniques.\u003cbr\u003e\r\n•Quick and simple automation-friendly protocol; no thermal cycler required.\u003cbr\u003e\r\n•Yields high-quality DNA (e.g., for high-throughput genotyping, hybridization, and DNA archival).\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription\u003cbr\u003e\r\nGenomiPhi HY DNA Amplification Kit is part of the Phi29 DNA polymerase family of products from Cytiva. It contains all of the components necessary for midi-scale whole genome amplification by isothermal strand displacement amplification.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAmplification is highly uniform over the entire genome so that locus representation remains extremely close to the original DNA sample. Furthermore, amplification is carried out with very high fidelity due to Phi29 DNA polymerase proofreading activity.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe GenomiPhi HY DNA Amplification Kit procedure is quick, simple and does not require a thermal cycler. A typical DNA yield of 40 to 50 µg DNA can be achieved in four h with little hands-on time. The average product length is over 10 kb. The starting material for GenomiPhi reactions can be purified DNA from any commercial kit or homebrew method, or a nonpurified cell lysate may be used. The kit was verified with DNA from various clinical samples including blood and buccal swabs. GenomiPhi amplified DNA is suitable for various applications such as genotyping (SNP, STR, array CGH), cloning, sequencing, and DNA archiving.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775948869923,"sku":"CYTI25660020","price":3005.5,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/25660020.jpg?v=1789940753"},{"product_id":"templiphi-sequence-resolver-kit-200-reactions","title":"TempliPhi sequence resolver kit, 200 reactions","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nTempliPhi™ Sequence Resolver Kit resolves most of the sequencing stops or gaps that routinely elude other commonly used finishing methods. The use of this kit eliminates the need to use dGTP chemistry, which can affect the accuracy of a sequence due to the appearance of sequence compression. In addition, it eliminates the need for additives in the sequencing reaction.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For the amplification of difficult templates for successful DNA sequencing.\u003cbr\u003e\r\n•Solve the most common sequencing problems such as repeats, sequencing stops, and compressions with a single kit.\u003cbr\u003e\r\n•Improve difficult template sequencing success with up to 820 bp Phred 20 read length.\u003cbr\u003e\r\n•Cultureless preparation from bacterial colonies, glycerol stock or purified DNA; saves time and reagents.\u003cbr\u003e\r\n•Easy-to-use kit requires only 20 min hands-on time.\u003cbr\u003e\r\n•Amplified DNA can be directly used in sequencing reactions.\u003cbr\u003e\r\n•TempliPhi Sequence Resolver Kit produces exceptional sequencing results from difficult templates such as those with high GC content and secondary structures.\u003cbr\u003e\r\n•The kit resolves most of the sequencing stops or gaps that routinely elude other commonly used finishing methods.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTrends in rolling circle amplification: Capabilities for manipulation, error free production and assembly of nucleic acids are advancing. \u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription\u003cbr\u003e\r\nThe kit can be used with both small (e.g., plasmids and M13) and large (fosmids and bacterial artificial chromosomes [BACs]) circular templates. The starting template for the reaction can be purified DNA, glycerol stock, liquid culture, or colonies. The reaction takes less than 20 min to prepare and after an overnight incubation at 10°C, it is ready to be used directly in sequencing applications with the sequencing chemistry of choice. A ten microliter (10 µl) reaction typically yields 1 µg of DNA in a standard overnight reaction.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775949394211,"sku":"CYTI28903531","price":3469.9,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/28903529.jpg?v=1789944614"},{"product_id":"gfx-96-pcr-purification-kit-10-x-96-well-plates","title":"GFX 96 PCR Purification Kit","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nKit uses glass fiber matrix technology in a 96-well format for highly efficient purification of PCR products. DNA fragments from PCR are captured by the matrix in presence of a chaotropic salt and contaminants are removed by washing matrix.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For the purification of up to 96 PCR products (0.1 to 10 kb) simultaneously in as little as 15 min.\u003cbr\u003e\r\n•High yields of pure DNA recovered in a small volume of water or a low ionic strength buffer.\u003cbr\u003e\r\n•Typical recoveries are \u0026gt; 85% for PCR products 100 bp to 10 kb in length; salt removal typically = 99%.\u003cbr\u003e\r\n•Prepacked glass fiber matrix 96-well plates are validated for use with Macherey-Nagel NucleoVac 96 vacuum manifold.\u003cbr\u003e\r\n•Avoids ethanol precipitations and hazardous organic extractions.\u003cbr\u003e\r\n•Purified DNA is ready for use in most applications, including fluorescent sequencing, microarrays, labeling, hybridization, ligation, and transformation.\u003cbr\u003e\r\n\u003cbr\u003e\r\nGFX 96 Purification Kit utilizes glass fiber matrix technology in a 96-well format for highly efficient purification of PCR products. Fragments from PCR are captured by the matrix in the presence of a chaotropic salt, and contaminants are conveniently removed by washing the matrix with a buffered ethanol solution.\u003cbr\u003e\r\n\u003cbr\u003e\r\nGFX 96 PCR Purification Kit contains the following components in sufficient quantities: binding plates, wash plates, collection plates, color-coded bottles of capture buffer, wash buffer, and a choice of two elution buffers (Tris-HCl and sterile water), and an instruction booklet.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775949492515,"sku":"CYTI28903445","price":2413.6,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/28903445.jpg?v=1789944616"},{"product_id":"templiphi-2000-reaction-kit","title":"TempliPhi 2000 Reaction Kit","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nTempliPhi 2000 Reaction Kit\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Prepare circular DNA templates for cycle sequencing, cloning, and transformation in 4 to 6 h.\u003cbr\u003e\r\n•Generate microgram quantities of template DNA from picogram amounts of starting material.\u003cbr\u003e\r\n•Use amplified DNA directly for cycle sequencing without purification.\u003cbr\u003e\r\n•Amplify DNA from bacterial or M13 liquid cultures, colonies, plaques, glycerol stocks, or purified circular (plasmid or M13) DNA.\u003cbr\u003e\r\n•Simple protocol reduces time, labor, and consumables needed for template preparation, and workflow enables easy automation.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTrends in rolling circle amplification: Capabilities for manipulation, error free production and assembly of nucleic acids are advancing. \u003cbr\u003e\r\n\u003cbr\u003e\r\nTempliPhi Kits use a unique process to efficiently prepare micrograms of circular DNA from picogram input material. The DNA templates are prepared by rolling circle amplification (RCA) using bacteriophage Phi29 DNA polymerase. TempliPhi uses an isothermal method for the exponential amplification of circular DNA. Phi29 DNA polymerase is active at 30°C, enabling amplification to be performed at this temperature without the need for thermal cycling. The TempliPhi protocol requires less than 20 min of hands-on time to amplify 96 samples from bacterial colonies.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTwo different types of TempliPhi DNA Amplification Kits are available to meet different throughput requirements. TempliPhi DNA Amplification Kit for 2000 reactions contains premixed components and generates templates after overnight incubation. The 100- and 500-reaction kits contain separate, unmixed components for enhanced stability.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe TempliPhi DNA Sequencing Template Amplification Kit has a distinct protocol and workflow compared to the 100\/500 reaction size. Procedures for each kit are not interchangeable. Prior optimization is needed.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775949590819,"sku":"CYTI28964286","price":5205.8,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/28964286.jpg?v=1789945223"},{"product_id":"sephadex-g-50-m-dna-grade-100-g","title":"Sephadex G-50 M DNA Grade, 100g","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nSephadex G-50 M DNA Grade\u003cbr\u003e\r\nSephadex™ G-50 M DNA Grade chromatography resin for purification of DNA fragments up to 20 bases in length from small molecules such as salts by size exclusion. DNA fragments above 20 bases will be excluded from the resin and will pass through without retention compared to smaller molecules. The media is provided in bulk (dry) format to allow researchers to prepare their own columns for purifying nucleic acids. The product is tested to ensure reproducibility and high recovery of DNA (\u0026gt; 90%).\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775949689123,"sku":"CYTI17004502","price":556.7,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/17004502.jpg?v=1789940119"},{"product_id":"sephadex-g-50-dna-grade-f-100-g","title":"Sephadex G-50 DNA Grade F, 100g","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nSephadex G-50 grade F is a size exclusion chromatography resin designed for desalting and buffer exchange, and for purification of DNA and oligonucleotides greater than 20 bases in length using spin columns.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For purification of DNA from small molecules by size exclusion\u003cbr\u003e\r\n•Tested to ensure reproducibly high recovery of DNA\u003cbr\u003e\r\n•Sephadex G-50 DNA Grade is used in various G-50 columns, such as AutoSeq G-50 columns, ProbeQuant G-50 Micro Columns, MicroSpin G-50 Columns, and NICK Columns\u003cbr\u003e\r\n•Suitable for researchers who prefer to prepare their own columns for purifying nucleic acids\u003cbr\u003e\r\n•Excellent for rapid purification of newly synthesized oligonucleotides \u0026gt; 10-mers, including oligonucleotide probes, in 100 to 150 µL of deprotection solution using spin-column chromatography\u003cbr\u003e\r\n•Useful for desalting or buffer exchange of DNA and removal of unincorporated radionucleotides from end-labeled oligonucleotides (at least 10 bases in length) in a volume of 10 to 100 µL\u003cbr\u003e\r\n\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-50 is one of five different G-types ranging from G-10 for small molecules to G-75 for larger molecules. Sephadex G-50 is a well-established gel filtration resin for desalting and buffer exchange of biomolecules \u0026gt; 30 000 molecular weight, and with a spin protocol can be used for DNA and oligo purification of molecules greater than 20 bases in length.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAlternatively, Sephadex G-25 can be used. Sephadex G-25 has an exclusion limit of approximately Mr 5000, and with a spin protocol this means it can be used for any DNA greater than 10 bases in length.\u003cbr\u003e\r\n\u003cbr\u003e\r\nBoth types of Sephadex are therefore highly suitable for the purification of oligonucleotides or very small DNA fragments following synthesis or a labeling reaction.\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin columns packed with Sephadex G-50 DNA Grade are suitable for the rapid purification of DNA, for use in a wide range of applications, including desalting DNA, buffer exchange, and removal of unincorporated nucleotides from end-labelled oligonucleotides.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-25 DNA Grade and Sephadex G-50 DNA Grade are sold separately.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is a Sample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775949787427,"sku":"CYTI17057302","price":554.0,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/17057302.jpg?v=1789940122"},{"product_id":"probequant-g-50-micro-columns","title":"ProbeQuant G-50 Micro Columns","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nProbeQuant G-50 Micro Columns use spin-column chromatography to provide a fast and reliable method for the preparation of DNA probes, separating them from unincorporated labeled nucleotides.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•For rapid purification of labeled DNA (= 20 bases) from unincorporated labeled nucleotides in a volume of 25 to 50 µL using spin-column chromatography\u003cbr\u003e\r\n•Prepacked with Sephadex G-50 DNA Grade and pre-equilibrated in STE containing 0.15% Kathon CG\/ICP Biocide for convenience\u003cbr\u003e\r\n•Ready to use and requires less than 4 minutes from sample application to collection of purified product\u003cbr\u003e\r\n•Designed for use in a microcentrifuge\u003cbr\u003e\r\n•Tested in assays: nickase, single and double-stranded exonuclease and RNase\u003cbr\u003e\r\n\u003cbr\u003e\r\n\u003cbr\u003e\r\nProbeQuant G-50 Micro Columns use spin-column chromatography to provide a fast and reliable method for purifying labeled probes from unincorporated labeled nucleotides. In addition, a portion of the eluted DNA can be counted in a scintillation counter and compared to an unpurified sample to give an approximation of percent incorporation.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe columns are designed for use in a microcentrifuge, come prepacked with Sephadex G-50 DNA grade and are pre-equilibrated in STE, which means that they are ready to use. They can accommodate samples ranging in volume from 25 µL to 50 µL.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe resin used in these columns, Sephadex G-50 DNA Grade, can be used in a wide range of applications, including desalting DNA, buffer exchange, and removal of unincorporated nucleotides from end-labelled oligonucleotides.\u003cbr\u003e\r\n\u003cbr\u003e\r\nMicroSpin columns packed with Sephadex G-50 DNA Grade are ideal for the rapid purification of DNA for use in a wide range of applications, including desalting DNA, buffer exchange, and removal of unincorporated nucleotides from end-labelled oligonucleotides .\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-50 is one of five different G-types ranging from G-10 for small molecules to G-75 for larger molecules. Sephadex G-50 is a well-established size exclusion chromatography resin for desalting and buffer exchange of biomolecules \u0026gt; 30 000 molecular weight, and with a spin protocol can be used for DNA and oligo purification of molecules greater than 20 bases in length.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAlternatively, Sephadex G-25 or Sephadex G-100 can be used. Sephadex G-25 has an exclusion limit of approximately Mr 5000, and with a spin protocol this means it can be used for any DNA greater than 10 bases in length.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSephadex G-100 DNA Grade has an exclusion limit of 25bp ds DNA.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAll these Sephadex types are therefore suitable for the purification of oligonucleotides or small DNA fragments following synthesis or a labeling reaction.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775949885731,"sku":"CYTI28903408","price":368.7,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/28903408.jpg?v=1789944619"},{"product_id":"sera-xtracta-virus-pathogen-kit-1000-extractions","title":"Sera-Xtracta Virus\/Pathogen Kit (1000 extractions)","description":"\u003cp\u003eGeneral description\u003cbr\u003e\r\nSera-Xtracta Virus\/Pathogen Kit for high-throughput total nucleic acid (DNA\/RNA) isolation from bacteria and viruses including Adenovirus (Type 14), Influenza A (H3N2) and COVID-19.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSera-Xtracta Virus\/Pathogen Kit provides a simple and rapid method to optimize the workflow for sensitive detection of viruses and other pathogens found in low concentrations.\u003cbr\u003e\r\n\u003cbr\u003e\r\nInfectious diseases affect millions of people every year. Particularly virulent and multi-drug resistant agents are increasingly responsible for infections with ever-expanding complexities. The design, manufacture and validation of assays for these pathogenic agents requires the successful purification of high-quality nucleic acid. This is essential to any molecular research and testing workflow. The nucleic acid purification process can be a bottleneck because sufficient nucleic acid from biological samples is required to meet a sensitivity threshold for assays which are designed to help identify, map or make informed decisions on latent and active infections.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe Sera-Xtracta Virus\/Pathogen kit is for research use only (RUO).\u003cbr\u003e\r\n\u003cbr\u003e\r\nOptimize isolation workflows to reduce bottlenecks\u003cbr\u003e\r\n\u003cbr\u003e\r\nTo address this bottleneck, our robust extraction chemistry ensures that the total nucleic acid is selectively bound to the superparamagnetic beads, while impurities are efficiently removed during the quick wash steps. The resulting high quality total nucleic acid is then eluted from the bead using a suitable elution buffer of choice. The rapid Sera-Xtracta workflow gives pure, high-quality nucleic acid suitable for sensitive molecular testing.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe Sera-Xtracta Virus\/Pathogen Kit is supported by Cytiva’s expertise in Sera-Mag bead technology. The formulation can be customized and modified to meet your specific requirements.\u003cbr\u003e\r\n\u003cbr\u003e\r\nHave you considered your magnetic separation rack? Cytiva’s Magnetic Separation Rack 15 mL is a 3D printed, magnetized tube rack with a strong, removable magnetic force and easy pipette access. It facilitates high capture, retention, and release of magnetic beads from various liquid sample media, allowing high-throughput, parallel processing of up to six 15 mL samples.\u003cbr\u003e\r\n\u003cbr\u003e\r\nFeatures and Benefits\u003cbr\u003e\r\n•Offers the advantages of solid phase extraction (using magnetic beads) and reproducible yields\u003cbr\u003e\r\n•Simplified protocol can be adapted for both manual and automated high-throughput processing\u003cbr\u003e\r\n•Scalable up to 400 µL of sample\u003cbr\u003e\r\n•Rapid extraction procedure can be completed in less than 30 minutes\u003cbr\u003e\r\n•For use with respiratory biological matrices, blood and Universal transport media to support the sensitive downstream detection of viruses and other pathogens found in low concentrations\u003cbr\u003e\r\n•Compatible with molecular biology techniques, including quantitative polymerase chain reaction (qPCR, RT-qPCR), Droplet digital PCR (ddPCR), and next-generation sequencing (NGS).\u003cbr\u003e\r\n•1000 Purifications\u003cbr\u003e\r\n\u003cbr\u003e\r\nLegal Information\u003cbr\u003e\r\nCytiva is a registered trademark of Global Life Sciences IP Holdco LLC or an affiliate\u003cbr\u003e\r\nSera-Xtracta is a trademark of Global Life Sciences IP Holdco LLC\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775949951267,"sku":"CYTI29514201","price":4125.0,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29514201.jpg?v=1789938314"},{"product_id":"ready-to-go-t4-dna-ligase-50-reaction-beads","title":"Ready-To-Go T4 DNA Ligase, 50 reaction beads","description":"\u003cp\u003eOverview\u003cbr\u003e\r\nReady-To-Go T4 DNA Ligase catalyzes the formation of a phosphodiester bond between the 5''-phosphoryl group and the 3''-hydroxyl group of two double-stranded DNA fragments.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•Covalently-linking DNA fragments takes only 30 minutes.\u003cbr\u003e\r\n•Single-dose, ambient temperature stable reaction mixes.\u003cbr\u003e\r\n\u003cbr\u003e\r\nReady-To-Go T4 DNA Ligase includes self-circularization of linear DNA prior to transformation, ligation of insert to vector, and ligation of synthetic linkers to blunt-ended DNA.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAdenosine triphosphate (ATP) is required for this reaction. Ligation of blunt-ended DNA is greatly stimulated by polyethylene glycol.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775950049571,"sku":"CYTI27036101","price":1096.1,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/27036101.jpg?v=1789940755"},{"product_id":"genomiphi-v3-ready-to-go-dna-amplification-kit-24-reactions","title":"GenomiPhi V3 Ready-To-Go DNA amplification kit, 24 reactions","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nGenomiPhi V3 Ready-To-Go DNA Amplification Kit offers highly efficient and representative whole-genome amplification with 12 to 20 µg yield from nanogram amounts of DNA sample.\u003cbr\u003e\r\n\u003cbr\u003e\r\nRepresentative amplification of the whole genome.\u003cbr\u003e\r\n•Preformulated, predispensed, single-dose, lyophilized cakes for rapid reaction set-up and greater reproducibility.\u003cbr\u003e\r\n•Quick and simple automation-friendly protocol; no thermal cycler required.\u003cbr\u003e\r\n•Shipping and storage at room temperature provides easy access and reduced carbon footprint.\u003cbr\u003e\r\n•Yields high-quality DNA (e.g. for high-throughput genotyping and DNA archival).\u003cbr\u003e\r\n\u003cbr\u003e\r\nDescription\u003cbr\u003e\r\nGenomiPhi V3 Ready-To-Go DNA Amplification Kit is part of the Phi29 DNA polymerase family of products from Cytiva. It contains all of the components necessary for whole genome amplification by isothermal strand displacement amplification. The reaction mixture is provided as predispensed, single-dose, lyophilized cakes in either strips of 8 tubes, or 96-well plates.\u003cbr\u003e\r\n\u003cbr\u003e\r\nAmplification is highly uniform over the entire genome so that locus representation remains extremely close to the original DNA sample. Furthermore, amplification is carried out with very high fidelity due to Phi29 DNA polymerase proofreading activity. The average product length is over 10 kb.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe GenomiPhi V3 Ready-To-Go DNA Amplification Kit procedure is quick, simple and does not require a thermocycler. A typical DNA yield of 12 to 20 µg DNA can be achieved in less than two hours from only 10 ng of genomic DNA input. The starting material for GenomiPhi reactions can be purified DNA from any commercial kit or homebrew method, or a nonpurified cell lysate may be used. Protocols for the amplification of DNA from blood lysates and dried blood spots are included in the manual.\u003cbr\u003e\r\n\u003cbr\u003e\r\nGenomiPhi amplified DNA is suitable for various applications such as genotyping (SNP, STR, array CGH), cloning, sequencing, and DNA archival.\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775950147875,"sku":"CYTI29013586","price":296.4,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29013586_efa6df26-de46-4116-82d5-8a7b52bd2261.jpg?v=1789945523"},{"product_id":"serasil-mag™-400-beads-1l","title":"SeraSil-Mag™ 400 beads 1L","description":"\u003cp\u003eOverview:\u003cbr\u003e\r\nSeraSil-Mag™ silica coated superparamagnetic beads for nucleic acid isolation deliver high purity DNA extraction for highly sensitive applications where sample is scarce. These beads provide an optimal surface for nucleic acid binding with high performance and low background.\u003cbr\u003e\r\n\u003cbr\u003e\r\n•High magnetization (60 emu\/g) and strong binding capacity giving fast magnetic response (~5 secs) and shorten time required for magnetic steps during isolation.\u003cbr\u003e\r\n•Beads come in two sizes (submicroscale diameter 700 nm and 400 nm), offering choice based on surface requirements and high binding capacity due to the small sized particles.\u003cbr\u003e\r\n•Beads are monodispersed with narrow size distribution for consistent, reproducible results.\u003cbr\u003e\r\n•Silanol hydroxyl groups on the bead surface give efficient, high purity isolation of nucleic acids.\u003cbr\u003e\r\n•Tested for microbial contamination.\u003cbr\u003e\r\n•Good buoyancy stability (low sedimentation rate): beads remain well suspended and dispersed for over 90 mins (at 1 mg\/mL concentration),* providing good handling and suitability for automation. *Beads may settle faster at higher concentration.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSeraSil-Mag™ beads are compatible with chaotropic salt chemistry and vortex mixing, roller mixing and sonication.\u003cbr\u003e\r\n\u003cbr\u003e\r\nTightly controlled production processes result in core-shell beads which are uniform and spherical. The silica shell provides a high content of silanol surface groups and encloses the magnetic core. The submicron size allows for a high surface area and abundant binding sites. The narrow particle size distribution assures uniformity and consistency of the beads.\u003cbr\u003e\r\n\u003cbr\u003e\r\nThe magnetic nanoparticles within the core provide superparamagnetic properties to the SeraSil-Mag beads, resulting in extremely fast magnetic separation in the presence of a magnet. There is no residual magnetization when the magnetic field is removed, which further contributes to ease of handling during use.\u003cbr\u003e\r\n\u003cbr\u003e\r\nSeraSil-Mag™ beads are supported by Cytiva''s expertise in Sera-Mag™ bead technology and can be customized to your needs at our manufacturing centre of excellence in Cardiff.\u003cbr\u003e\r\n\u003cbr\u003e\r\nHave you considered your magnetic separation rack?\u003cbr\u003e\r\nCytiva’s Magnetic Separation Rack 15 mL is a 3D printed, magnetized tube rack with a strong, removable magnetic force and easy pipette access. It facilitates high capture, retention, and release of magnetic beads from various liquid sample media, allowing high-throughput, parallel processing of up to six 15 mL samples.\u003cbr\u003e\r\n\u003cbr\u003e\r\nFind out more about magnetic separation racks\u003cbr\u003e\r\n\u003cbr\u003e\r\nOur ISO 13485 accredited manufacturing center of excellence adheres to the standards in the manufacturing process, ensuring the highest quality and compliance with international medical device regulations.\u003cbr\u003e\r\n\u003cbr\u003e\r\n**Image is a Sample Only**\u003c\/p\u003e","brand":"Cytiva","offers":[{"title":"Default Title","offer_id":54775950246179,"sku":"CYTI29705862","price":9440.1,"currency_code":"NZD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/files\/29705862.jpg?v=1789946123"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0597\/5896\/9012\/collections\/CYTIVA_20logo_0aa9d44b-2e8b-43e7-bc69-873396fefae3.jpg?v=1772145991","url":"https:\/\/onelab.co.nz\/collections\/molecular-and-immunodiagnostics.oembed","provider":"Onelab","version":"1.0","type":"link"}