分子信标
实时聚合酶链反应
聚合酶链反应优化
聚合酶链反应
多路复用
PCR的应用
多重聚合酶链反应
计算生物学
化学
DNA
分子生物学
底漆(化妆品)
计算机科学
生物化学
生物
遗传学
寡核苷酸
基因
有机化学
作者
Jacqueline A. M. Vet,Salvatore A. E. Marras
出处
期刊:Humana Press eBooks
[Humana Press]
日期:2004-08-27
卷期号:: 273-290
被引量:67
标识
DOI:10.1385/1-59259-823-4:273
摘要
During the last few years, several innovative technologies have become available for performing sensitive and accurate genetic analyses. These techniques use fluorescent detection strategies in combination with nucleic acid amplification protocols. Most commonly used is the real-time polymerase chain reaction (PCR). To achieve the maximum potential of a realtime PCR assay, several parameters must be evaluated and optimized independently. This chapter describes the different steps necessary for establishing a molecular beacon real-time PCR assay: (1) target design, (2) primer design, (3) optimization of the amplification reaction conditions using SYBR Green, (4) molecular beacon design, and (5) molecular beacon synthesis and characterization. The last section provides an example of a multiplex quantitative real-time PCR.
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