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TaqDNA |产品详情|进口橙子视频旧款采购网




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    上海橙子视频app安卓下载生物科技公司
    Tel:400-968-7988    021-33779008
    TaqDNA
    品牌:Prospec
    货号:
    规格:1,000U
    货期:

    TaqDNA

    商品详情 参考文献 相关资料

    Catalogue number

    ENZ-308

    Synonyms

    DNA polymerase I thermostable, EC 2.7.7.7, Taq polymerase 1.

    Description

    Taq DNA Polymerase(a) is a thermostable enzyme of approximately 95 kDa isolated from Thermus aquaticus. This unmodified enzyme replicates DNA at 74°C and exhibits a half-life of 40 minutes at 95°C. The enzyme catalyzes the polymerization of nucleotides into duplex DNA in the 5´~3´ direction in the presence of magnesium and also possesses a 5´~3´ exonuclease activity. Taq DNA Polymerase is recommended for use in PCR but is not recommended for use in DNA sequencing reactions.

    Source

    Recombinant e.coli contains Thermus aquaticus polymerase gene.

    Formulation

    Taq DNA Polymerase solution in 20mM Tris-HCl, pH 8.0, 100mM KCl, 0.1mM EDTA, 1mM DTT, 50% Glycerol, 0.5% NP40, 0.5% Tween 20.

    Unit Definition

    One unit is defined as the amount of enzyme required to catalyze the incorporation of 10nmol of dNTP into acid-insoluble material in 30 minutes at 74°C. The reaction conditions are: 50mM Tris-HCl (pH 9.0 at 25°C), 50mM NaCl, 5mM MgCl2, 200µm each of dATP, dCTP, dGTP, dTTP (a mix of unlabeled and [3H]dTTP), 10µg activated calf thymus DNA and 0.1mg/ml BSA in a final volume of 50ul.

    10X Reaction Buffer with MgCl2

    500mM KCl, 100mM Tris-HCl (pH 9.0 at 25C), 1% Triton X-100 and 15mM MgCl2. Buffer is optimized for use with 0.2mM of each dNTP.

    10X Reaction Buffer without MgCl2

    500mM KCl, 100mM Tris-HCl (pH 9.0 at 25C) and 1% Triton X-100. Include: 10X Reaction Buffer without MgCl2 and separate 25mM MgCl2 Solution.

    Note

    Depend on an Enzyme That Works: Compositions of the storage buffers have been optimized to assure quality performance of the enzyme under a variety of conditions.

    Specify Your Own Reaction Conditions

    Choose either Taq with Mg-free 10X Reaction Buffer and separate 25mM MgCl2 or Taq with 10X Reaction Buffer containing 15mM MgCl2.

    Rely on a Performance-Tested Enzyme

    Our PCR systems, enzymes and reagents are proven in PCR to ensure reliable, high-performance results. If you are not completely satisfied with any of our PCR product, we will send a replacement or refund your account.

    Stability

    Stable for 5 days at 10°C, for longer period of time store at -20°C.

    Storage Buffer

    Compatibility with Reaction Buffers: Taq DNA Polymerase in Storage Buffer. Use of other reaction buffers that do not contain Triton X-100 (final concentration of 0.1%) will result in inactivation of the enzyme.
    50mM Tris-HCl (pH 8.0), 100mM NaCl, 0.1mM EDTA, 1mM DTT, 50% glycerol and 1% Triton X-100.

    Purity

    Greater than 95.0% as determined by SDS-PAGE.

    Safety Data Sheet

    SDS

    Usage

    Prospec's products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
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