一个集成流控电路中mRNA和microRNA靶点的联合RT-qPCR。

D. Baldwin, A. Horan, Patrick J. Hesketh, S. Mehta
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引用次数: 2

摘要

使用单一分析方法分析同一样品中大量mRNA和microRNAs (miRNAs)表达水平的能力,将有助于研究miRNA对mRNA丰度的影响,并简化跨多种RNA类别的生物标志物筛选。本文描述了长RNA和miRNA靶标的逆转录方案,随后对合并的cdna进行分析前扩增,并对混合的候选RNA生物标志物进行定量PCR (qPCR)检测。该方法为设计定制靶板提供了灵活性,在输入RNA量的范围内具有鲁棒性,并证明了高检测成功率。
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Combined RT-qPCR of mRNA and microRNA Targets within One Fluidigm Integrated Fluidic Circuit.
The ability to profile expression levels of a large number of mRNAs and microRNAs (miRNAs) within the same sample, using a single assay method, would facilitate investigations of miRNA effects on mRNA abundance and streamline biomarker screening across multiple RNA classes. A protocol is described for reverse transcription of long RNA and miRNA targets, followed by preassay amplification of the pooled cDNAs and quantitative PCR (qPCR) detection for a mixed panel of candidate RNA biomarkers. The method provides flexibility for designing custom target panels, is robust over a range of input RNA amounts, and demonstrated a high assay success rate.
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