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Method of polymerase chain reaction with ultra-low denaturing temperatures and applications thereof

机译:超低变性温度的聚合酶链反应方法及其应用

摘要

The invention relates to a method polymerase chain reaction (PCR) and the application thereof A method of PCR performed at ultra-low denaturing temperatures is provided. The denaturing temperatures of the templates adopted are 93-98° C. in the primary 2-3 cycles, and 60-87° C. in the follow-up cycles, those are much lower than 94-96° C., the conventional denaturing temperatures. It is found in the experiment that this method could not only become a universally applied PCR, but also control the reaction specificity by the template selection at ultra-low temperatures. The method possesses unique functions in excluding non-specific amplified products and false-negative results, excluding false-positivity brought about by the contaminants in products and discriminating genomic DNA from cDNA.
机译:本发明涉及聚合酶链反应(PCR)方法及其应用。提供了一种在超低变性温度下进行的PCR方法。所采用模板的变性温度在最初的2-3个循环中为93-98°C,在后续循环中为60-87°C,远低于传统的94-96°C变性温度。在实验中发现,该方法不仅可以成为通用的PCR方法,而且还可以通过在超低温下选择模板来控制反应特异性。该方法在排除非特异性扩增产物和假阴性结果,排除产物中的污染物引起的假阳性以及从cDNA区分基因组DNA方面具有独特的功能。

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