逆转录酶
逆转录聚合酶链式反应
互补DNA
聚合酶链反应
分子生物学
实时聚合酶链反应
RNA提取
生物
核糖核酸
基因表达
基因
计算生物学
化学
遗传学
作者
Sharon Glaysher,Francis G Gabriel,Ian A. Cree
出处
期刊:Methods in molecular biology
日期:2011-01-01
卷期号:: 381-393
被引量:7
标识
DOI:10.1007/978-1-61779-080-5_31
摘要
Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) offers a robust method for the measurement of RNA levels for any gene within cells harvested at any point before or during cell culture. The key elements of RNA extraction followed by a two-step qRT-PCR method (reverse transcription and PCR) are described, followed by a brief section on analysis of the results. There are a number of excellent kits available commercially for much of this work, but it is essential to ensure that the quality and quantity of cDNA produced is adequate for the standard PCR or array to be used.
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