检出限
小RNA
化学
实时聚合酶链反应
计算生物学
色谱法
逆转录酶
逆转录聚合酶链式反应
分子生物学
核糖核酸
基因
信使核糖核酸
生物
生物化学
作者
Jingli Yan,Nan Zhang,Qi Cui,Xiangjun Liu,Dihua Shangguan
出处
期刊:Talanta
[Elsevier BV]
日期:2013-02-20
卷期号:110: 190-195
被引量:33
标识
DOI:10.1016/j.talanta.2013.02.028
摘要
Rapid and simple methods for microRNA (miRNA) detection are essential for biological research of miRNAs and clinical diagnosis. Here we describe a sensitive and specific real time RT-PCR (also RT-qPCR) method for miRNA quantification. The whole detection process including reverse transcription and PCR is performed in one PCR tube by a one-step operation on a real-time PCR system. The results display a wide linear range from 0.1 amol to 10 fmol with a detection limit of 12.6 zmol for miRNA let-7a detection. Let-7a in small RNA samples extracted from tumor cells has been successfully detected by this method. This method is cost-effective, simple and rapid, and has the advantages in the high-throughput routing assay of given miRNAs, as well as in non-model research that has less specific kits and reagents.
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