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miR-CATCH:微小RNA捕获亲和技术。

miR-CATCH: microRNA capture affinity technology.

作者信息

Vencken Sebastian, Hassan Tidi, McElvaney Noel G, Smith Stephen G J, Greene Catherine M

机构信息

Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland.

出版信息

Methods Mol Biol. 2015;1218:365-73. doi: 10.1007/978-1-4939-1538-5_23.

Abstract

Several experimental methods exist to explore the microRNA (miRNA) regulome. These methods almost exclusively focus on multiple targets bound to a single, or perhaps a few miRNAs of interest. Here, we describe a microRNA capture affinity technology (miR-CATCH) which uses an affinity capture oligonucleotide to co-purify a single target messenger RNA (mRNA) together with all its endogenously bound miRNAs. This bench-top method is similar to RNA immunoprecipitation (RIP) and provides an experimental alternative to computational miRNA target prediction.

摘要

有几种实验方法可用于探索微小RNA(miRNA)调控组。这些方法几乎都只关注与单个或少数几个感兴趣的miRNA结合的多个靶标。在此,我们描述了一种微小RNA捕获亲和技术(miR-CATCH),该技术使用亲和捕获寡核苷酸将单个靶标信使核糖核酸(mRNA)与其所有内源性结合的miRNA一起共纯化。这种台式方法类似于RNA免疫沉淀(RIP),为计算miRNA靶标预测提供了一种实验替代方法。

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