| Literature DB >> 28439839 |
Emma Bell1,2, Hannah L Watson1, Shivani Bailey1, Matthew J Murray3,4,5, Nicholas Coleman6,7.
Abstract
Reverse-transcriptase quantitative PCR (RT-qPCR) is a widely used method for quantifying microRNAs (miRNAs) in cells and tissues. However, the quantification of miRNAs in the circulation presents specific challenges. Here, we describe an optimized protocol using a small amount of input material to assess serum sample quality and quantify levels of a panel of up to 20 miRNAs. This is achieved by multiplexing Taqman miRNA stem-loop primers in the reverse transcription step. An additional multiplexed pre-amplification step is used to increase the sensitivity of the final quantification step, which is carried out using standard Taqman qPCR methodology.Keywords: Cerebrospinal fluid; MicroRNA; Plasma; Pre-amplification; RT-qPCR; Serum
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Year: 2017 PMID: 28439839 DOI: 10.1007/978-1-4939-6866-4_18
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745