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PCR METHOD AND APPLICATION BY TRANSNORMAL LOW THERMO-DENATURATION TEMPERATURE

机译:超常低温还原温度的PCR方法及应用

摘要

The present invention relates to a method for polymerase chain reaction and application. It provides means for PCR amplification by transnormal low thermo­-denaturation temps which do not demand the use of DNA denaturant. The denaturation temperature of template can be used as follow: 93-98°C during first two or three cycles, and 60-87°C during continued cycles which transnormal low than normal denaturation temperature of 94-96°C. We discovered that this PCR method can be used widespread, and by means of the selective denaturation of template at transnormal temperature, we can control specificity of reaction, so this method can use for obviating unspecific PCR products, false negative result, false positive result comed from contamined products, and the method can used for distinguishing between gene DNA and cDNA.
机译:本发明涉及一种聚合酶链反应的方法和应用。它提供了通过超常低热变性温度进行PCR扩增的方法,该方法不需要使用DNA变性剂。模板的变性温度可以如下使用:前两个或三个循环中的93-98°C,以及连续循环中的60-87°C,这些温度通常低于正常变性温度94-96°C。我们发现这种PCR方法可以广泛使用,并且通过在正常温度下模板的选择性变性,我们可以控制反应的特异性,因此该方法可以用于消除非特异性PCR产物,出现假阴性结果,假阳性结果。该方法可用于区分基因DNA和cDNA。

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