Thornton Brenda, Basu Chhandak
School of Biological Sciences, University of Northern Colorado, Greeley, Colorado 80639, USA.
Biochem Mol Biol Educ. 2011 Mar-Apr;39(2):145-54. doi: 10.1002/bmb.20461.
Real-time PCR (quantitative PCR or qPCR) has become the preferred method for validating results obtained from assays which measure gene expression profiles. The process uses reverse transcription polymerase chain reaction (RT-PCR), coupled with fluorescent chemistry, to measure variations in transcriptome levels between samples. The four most commonly used fluorescent chemistries are SYBR® Green dyes and TaqMan®, Molecular Beacon or Scorpion probes. SYBR® Green is very simple to use and cost efficient. As SYBR® Green dye binds to any double-stranded DNA product, its success depends greatly on proper primer design. Many types of online primer design software are available, which can be used free of charge to design desirable SYBR® Green-based qPCR primers. This laboratory exercise is intended for those who have a fundamental background in PCR. It addresses the basic fluorescent chemistries of real-time PCR, the basic rules and pitfalls of primer design, and provides a step-by-step protocol for designing SYBR® Green-based primers with free, online software.
实时PCR(定量PCR或qPCR)已成为验证从测量基因表达谱的检测中获得的结果的首选方法。该过程使用逆转录聚合酶链反应(RT-PCR),结合荧光化学,来测量样品之间转录组水平的变化。四种最常用的荧光化学方法是SYBR® Green染料和TaqMan®、分子信标或蝎形探针。SYBR® Green使用非常简单且成本效益高。由于SYBR® Green染料可与任何双链DNA产物结合,其成功很大程度上取决于合适的引物设计。有许多类型的在线引物设计软件可供使用,可免费用于设计理想的基于SYBR® Green的qPCR引物。本实验室练习面向那些具有PCR基础背景的人。它介绍了实时PCR的基本荧光化学方法、引物设计的基本规则和陷阱,并提供了使用免费在线软件设计基于SYBR® Green的引物的分步方案。