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A standard additions method reduces inhibitor-induced bias in quantitative real-time PCR

机译:标准添加方法可减少定量实时PCR中抑制剂引起的偏倚

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摘要

A method of calibration for real-time quantitative polymerase chain reaction (qPCR) experiments based on the method of standard additions combined with non-linear curve fitting is described. The method is tested by comparing the results of a traditionally calibrated qPCR experiment with the standard additions experiment in the presence of 2 mM EDTA, a known inhibitor chosen to provide an unambiguous test of the principle by inducing an approximately twofold bias in apparent copy number calculated using traditional calibration. The standard additions method is shown to substantially reduce inhibitor-induced bias in quantitative real-time qPCR.
机译:描述了一种基于标准加法与非线性曲线拟合相结合的实时定量聚合酶链反应(qPCR)实验的校准方法。通过在2 mM EDTA存在下将传统校准的qPCR实验结果与标准添加实验进行比较来测试该方法,EDTA是一种已知抑制剂,通过在计算出的表观拷贝数上引起大约两倍的偏差来对原理进行明确测试使用传统的校准。在定量实时qPCR中,标准添加方法已显示可显着降低抑制剂引起的偏倚。

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