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Hybridase Thermostable RNase H

Hybridase Thermostable RNase H

Hybridase Thermostable RNase H,5U/µL500U

Specifically degrade the RNA in a DNA:RNA hybrid,without affecting DNA or unhybridised RNA,at higher reaction temperatures。

关键帧features

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  • 特定degrade the RNA in a DNA:RNA hybrid,without affecting DNA or unhybridised RNA,at higher reaction temperatures
  • Optimal activity above 65℃and maintains activity as high as 95℃
  • RNA in a RNA:DNA hybrid and will not digest free RNA or DNA
  • 主要决策和决策while minimising background due to nonspecific hybridisiation
选择大小
项目标识 H39500
TBD
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产品说明

Hybridase Thermostable RNase Hspecifically degrades the RNA in a DNA:RNA hybrid,without affecting DNA or unhybridized RNA.In contrast toE.coliRNase H,which is rapidly inactivated at55°C,Hybridase RNase H is active at high temperatures.It has optimal activity above65°C and can be used at temperatures up to 95°C。The thermostability of the enzyme permits it to be used at temperatures that give the highest hybridisation stringncy for specific DNA:RNA heteroduplexes,maximizing sensitivity and selectivity while minimizing background due to nonspecific hybridization。

应用程序,应用程序

  • High-stringency hybrid selection。
  • 诊断assays of specific target DNA sequences by isothermal probe amplification。
  • Transcription-based amplification methods(e.g.,NASBA®method)。
  • High-stringency mapping of mRNA structure。
  • Applications that require specific hydrolysis of the RNA in a DNA:RNA hybrid。

Unit Definition:One unit of Hybridase RNase H results in the acid-solubilization of 1nmol of polyadenylic acid in the presence of an equimolar concentration of polythymidylic acid in 20minutes at45°C under standard assay conditions。

Note: The unit assay is performed at 45°C because this is optimal for the Tmof poly(dT):poly(A)。The optimal temperature for many applications may be considerably high er。

存储缓冲器:50%glycerol containing 50mM Tris-HCl(pH7.5),0.1M NaCl,1.0mM DTT,0.1mM EDTA,and 0.1%Triton®X-100。

质量控制:Hybridase Thermostable RNase H is tested for RNA degradation in a RNA:DNA hybrid and for the absence of detectable exo-or endodeoxyribonuclease,and non-RNase H RNase activities。

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