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    ZymoTaq qPCR Premix

    E2054 / E2055

    ZymoTaq qPCR Premix

    Cat # Name Size
    E2054 ZymoTaq qPCR Premix 50 Rxns
    E2055 ZymoTaq qPCR Premix 200 Rxns



    • Hot-start polymerase for easy setup at room temperature.
    • Robust amplification of DNA for genotyping, SNP, and HRM analysis.
    • Strong fluorescent signal for real-time and quantitative PCR assays.

    ZymoTaq qPCR PreMix contains all the reagents needed to perform quantitative PCR and other molecular downstream analysis such as high-resolution melt (HRM) analysis of DNA methylation and other general real-time PCR assays. This premix features a hot-start DNA polymerase and buffer system optimized for the amplification of bisulfite-treated DNA. It also includes an intense dsDNA-specific fluorescent dye, SYTO 9, for sensitive real-time DNA quantification. This technology can also be found in the Femto Quantification Kits (E2005, E2006, E2007) for low copy detection of DNA from human, bacteria, or fungi.

    Activity 5' - 3' DNA polymerization
    Concentration Reaction conditions at 1X (50 µl total volume) will contain 2 U of ZymoTaq DNA polymerase.
    Equipment Real-time PCR can be performed on any instrument that has optical scanners that do not require passive reference dye.
    Storage Store at ≤ -20°C for up to 12 months. Minimize exposure to light. Avoid repeated freeze/thawing of reagents.
    Unit Definition One unit (U) enzyme of ZymoTaq DNA Polymerase is defined as the amount of enzyme required for the incorporation of 10 nmol dNTPs into an acid-insoluble form in 30 minutes at 72°C.

    The error rate for ZymoTaq DNA polymerase ranges from 1.1x10-4 to 8.9x10-5.

    The ZymoTaq DNA polymerase can amplify up to 5 kb.

    The ZymoTaq DNA PCR system utilizes a hot-start polymerase and is optimized for bisulfite PCR and other GC rich templates, as well as low-copy number of DNA templates. It can also be used for general molecular biology applications as well (e.g. suitable for TA cloning, multiplex PCR, etc).


    The ZymoTaq PreMix was specifically used to amplify bisulfite-treated DNA with no reports of inefficient or nonspecific amplification in a study of dynamic DNA methylation expression levels during different development stages. Results showed that timing of variations in methylation patterns were specific for genes related to growth.

    Fang X, et. al. (2013) Global and gene specific DNA methylation changes during zebrafish development. Comp Biochem Physiol B Biochem Mol Biol. 166(1):99-108.

    Cat # Name Size
    W1001-1 DNase/RNase-Free Water 1 ml

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