Real-time PCR分析mRNA表达

S. Bustin, T. Nolan
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引用次数: 22

摘要

过去几年中,基于荧光的实时逆转录聚合酶链反应(RT-qPCR)从一项实验技术转变为RNA检测和定量的主流科学工具,在基础研究、分子医学和生物技术中有着广泛的应用。试剂和仪器的不断改进,加上高通量和小型化的趋势,可能会加强这种卓越性,并继续开辟新的应用领域。尽管如此,尽管原则上无疑是一种简单的技术,但RT-qPCR分析的可靠性取决于一系列连续的步骤,包括仔细的实验设计、优化和验证,这些步骤必须实际实施,以获得有意义的、生物学相关的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of mRNA Expression by Real-time PCR
The last few years have witnessed the transformation of the real-time, fluorescence-based reverse transcription polymerase chain reaction (RT-qPCR) from an experimental technology into a mainstream scientific tool for the detection and quantification of RNA with an enormous range of uses in basic research, molecular medicine and biotechnology. The continuous improvement of reagents and instruments, combined with the trend towards high throughput and miniaturisation, is likely to reinforce that pre-eminence and continue to open up new application areas. Nonetheless, although in principle undoubtedly a straightforward technology, the reliability of RT-qPCR assays depends a series of sequential steps that include careful experimental design, optimisation and validation, which must be implemented pragmatically to obtain meaningful, biologically relevant data.
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