首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Real-time PCR method with statistical analysis to compare the potential of DNA isolation methods to remove PCR inhibitors from samples for diagnostic PCR.
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Real-time PCR method with statistical analysis to compare the potential of DNA isolation methods to remove PCR inhibitors from samples for diagnostic PCR.

机译:具有统计分析功能的实时PCR方法,用于比较DNA分离方法从样本中去除PCR抑制剂进行诊断性PCR的潜力。

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摘要

A real-time PCR method for fast comparison of different DNA isolation methods to remove PCR inhibitors from samples is presented. A fixed amount of target-200 copies of a 79-bp region of the COCH gene of the zebrafish (Danio rerio)-was added to each PCR reaction together with isolated DNA from different types of samples including chicken feces. Four commercial DNA isolation kits and a chelex-based technique were compared using this method. The copy numbers calculated and the endpoint fluorescence were statistically compared to the values of 22 control samples containing the control target and water instead of isolated DNA, processed together in the same PCR run. The level of the endpoint fluorescence was more often negatively influenced by inhibitors than the copy number calculated, suggesting a more pronounced effect on the plateau phase of the reaction by limiting one or more compounds in the PCR reaction.
机译:提出了一种实时PCR方法,用于快速比较不同的DNA分离方法,以从样品中去除PCR抑制剂。将固定量的斑马鱼(Danio rerio)COCH基因79 bp区域的target-200拷贝靶标与从不同类型样品(包括鸡粪)中分离出的DNA一起添加到每个PCR反应中。使用此方法比较了四种商业DNA分离试剂盒和基于chelex的技术。将计算的拷贝数和终点荧光值与22个含有对照靶标和水而不是分离的DNA的对照样品的值进行统计比较,这些样品在同一PCR运行中一起处理。与计算的拷贝数相比,终点荧光水平更经常受到抑制剂的负面影响,这表明通过限制PCR反应中的一种或多种化合物对反应平稳期的影响更为明显。

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