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High specific genotyping method using short target probe and helper probe

机译:使用短靶探针和辅助探针的高特异性基因分型方法

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Differentiating 1-bp differences using real-time PCR often leads to false-positive results. Therefore, we developed a fluorescence melting curve analysis (FMCA) method with a short target probe and helper probe labeled with a fluorophore and quencher, respectively. This fluorophore and quencher were designed to be near each other when the probes were hybridized to template DNA. The target probe was designed with a shorter length to facilitate a dramatic shift in melting temperature (Tm) upon encountering mismatched hybridization. In FMCA, when the temperature approached the target probe Tm, the target probe would begin to denature from the template DNA, and at the target probe Tm, the fluorescence signal increased markedly. Here, we examined 1-bp differences using the developed method with mitochondrial DNA from Larimichthys polyactis and Larimichthys crocea. Application of this method permitted specific genotype identification for all cases with no cross-reactivity, even when both templates were added to the same tube. (C) 2016 Elsevier Ltd. All rights reserved.
机译:使用实时PCR区分1-bp差异通常会导致假阳性结果。因此,我们开发了一种荧光熔解曲线分析(FMCA)方法,分别用短目标探针和辅助探针标记了荧光团和淬灭剂。当探针与模板DNA杂交时,该荧光团和淬灭剂被设计为彼此靠近。设计目标探针的长度较短,以便在遇到错配杂交时促进熔化温度(Tm)的急剧变化。在FMCA中,当温度接近目标探针Tm时,目标探针将开始从模板DNA变性,并且在目标探针Tm处,荧光信号显着增加。在这里,我们使用发达的线虫DNA和多头线虫的线粒体DNA用发达的方法检查了1-bp的差异。该方法的应用允许在没有交叉反应的所有情况下鉴定特定的基因型,即使将两个模板都添加到同一管中也是如此。 (C)2016 Elsevier Ltd.保留所有权利。

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