Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method

被引:156566
作者
Livak, KJ [1 ]
Schmittgen, TD
机构
[1] Washington State Univ, Dept Pharmaceut Sci, Pullman, WA 99164 USA
[2] Appl Biosyst Inc, Foster City, CA 94404 USA
关键词
reverse transcription polymerase chain reaction; quantitative polymerase chain reaction; relative quantification; real-time polymerase chain reaction; Taq Man;
D O I
10.1006/meth.2001.1262
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The two most commonly used methods to analyze data from real-time, quantitative PCR experiments are absolute quantification and relative quantification. Absolute quantification determines the input copy number, usually by relating the PCR signal to a standard curve. Relative quantification relates the PCR signal of the target transcript in a treatment group to that of another sample such as an untreated control. The 2(-DeltaDeltaCr) method is a convenient way to analyze the relative changes in gene expression from real-time quantitative PCR experiments. The purpose of this report is to present the derivation, assumptions, and applications of the 2(-DeltaDeltaCr) method. In addition, we present the derivation and applications of two variations of the 2(-DeltaDeltaCr) method that may be useful in the analysis of real-time, quantitative PCR data. (C) 2001 Elsevier science.
引用
收藏
页码:402 / 408
页数:7
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