摘要
实时荧光定量PCR是近年新兴的一项技术,因其快速、方便、便宜,需要DNA样品量少,无需放射性检测等优点被广泛应用于基因的定量分析。该文就实时荧光定量PCR(TaqMan)技术的发展、基本原理及测定外源基因拷贝数的技术流程做一介绍。
Real-time fluorescent quantitative PCR is a new technique which has been developed to be used in quantitative analysis of genes as well with the advantages of simpleness, quickness, short needs of target fragment DNA and none of hazardous radioisotopes in recent years. The development, the principle of real-time fluorescent quantitative PCR(TaqMan) and the techinical flow of estimating copy number of transgenic gene are introuduced in this paper.
出处
《广西植物》
CAS
CSCD
北大核心
2009年第3期408-412,共5页
Guihaia
基金
徐州师范大学科研基金(05XLB13)
徐州市科技局基金(XZ2006221)~~
关键词
外源基因
拷贝数
实时荧光定量PCR
transgenic gene
copy number real-time fluorescent quantitative PCR