逆转录酶SuperScript II,1万单位  Thermo 18064014 现货

逆转录酶SuperScript II,1万单位 Therm

o 18064014 现货
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  • 询价
  • Thermo
  • 18064014
  • 美国
  • 2025年10月11日
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    • 详细信息
    • 技术资料
    • 库存

      99

    • 保质期

      已收到实际货物为准

    • 供应商

      北京诺博莱德科技有限公司

    • 保存条件

      已收到实际货物为准

    货号: 18064014

     

    规格

    Optimal Reaction Temperature: 42° C
    Final Product Size(s): 12.3 kb or less
    Reverse Transcriptase: SuperScript® II
    Ribonuclease H Activity: Reduced
    Form: Frozen
    Format: Tube(s)
    Template: ssDNA, ssRNA, RNA-DNA Hybrid
    Sensitivity: Medium
    Product Size: 10,000 units
    Concentration: 200 U⁄µl
    Enzyme Function: RNA dependent DNA Polymerase
    Shipping Condition: Wet Ice
    Number of Reactions: 50 Reactions

     

    内容及储存

    SuperScript® II Reverse Transcriptase is supplied with a vial of 5X first-strand buffer [250 mM Tris-HCl (pH 8.3), 375 mM KCl, 15 mM MgCl2], and a vial of 100 mM DTT.

    Store at -20°C. Guaranteed stable for 6 months when properly stored.

     

    描述

    SuperScript® II Reverse Transcriptase (RT) is an improved version of SuperScript® RT. It is a DNA polymerase that synthesizes a complementary DNA strand from single-stranded RNA, DNA, or an RNA:DNA hybrid. This enzyme is genetically engineered by the introduction of point mutations in the RNase H active center to reduce RNase H activity. This structural modification eliminates degradation of RNA molecules during first-strand cDNA synthesis and gives SuperScript® II RT superior performance characteristics.

    • Yield – Reduced RNase H activity results in greater first-strand cDNA yields
    • Size of cDNA – Generation of RT-PCR products up to 12 kb
    • Thermostability – Full activity at 42°C
    • Flexibility – Uses either total or poly(A)+ RNA

    Performance and Quality Testing: SDS-PAGE purity; endodeoxyribonuclease, exodeoxyribonuclease, and ribonuclease assays; and yield and length of cDNA product.
    Unit Definition: One unit of SuperScript® II is the amount of enzyme required to incorporate 1 nmole of deoxyribonucleotide into acid-precipitable material in 10 min. at 37°C using poly(A)•oligo(dT)12-18 as template•primer (3).
    Unit Reaction Conditions: 50 mM Tris-HCl (pH 8.3), 40 mM KCl, 6 mM MgCl2, 1 mM DTT, 0.5 mM [3H]dTTP, 0.1 mM poly(A), 0.1 mM oligo(dT)12-18, 0.1 mg/ml BSA, and enzyme in 50 µl for 10 min. at 37°C.
    For Research Use Only. Not intended for any animal or human therapeutic or diagnostic use.

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