Dymond Jessica S
The High Throughput Biology Center and Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Methods Enzymol. 2013;529:279-89. doi: 10.1016/B978-0-12-418687-3.00023-9.
Quantitative PCR (qPCR), also called real-time PCR or quantitative real-time PCR, is a PCR-based technique that couples amplification of a target DNA sequence with quantification of the concentration of that DNA species in the reaction. This method enables calculation of the starting template concentration and is therefore a frequently used analytical tool in evaluating DNA copy number, viral load, SNP detection, and allelic discrimination. When preceded by reverse-transcription PCR, qPCR is a powerful tool to measure mRNA expression and is the gold standard for microarray gene expression data confirmation. Given the broad applications of qPCR and the many technical variations that have been developed, a brief survey of qPCR, including technical background, available chemistries, and data analysis techniques will provide a framework for both experimental design and evaluation.
定量聚合酶链反应(qPCR),也称为实时PCR或定量实时PCR,是一种基于PCR的技术,它将目标DNA序列的扩增与反应中该DNA种类浓度的定量相结合。该方法能够计算起始模板浓度,因此是评估DNA拷贝数、病毒载量、单核苷酸多态性检测和等位基因鉴别时常用的分析工具。当在逆转录PCR之前进行时,qPCR是测量mRNA表达的强大工具,也是微阵列基因表达数据确认的金标准。鉴于qPCR的广泛应用以及已开发的众多技术变体,对qPCR进行简要概述,包括技术背景、可用化学方法和数据分析技术,将为实验设计和评估提供一个框架。