Stem-loop RT-PCR quantification of siRNAs in vitro and in vivo.

Angie Cheng, Mu Li, Yu Liang, Yu Wang, Linda Wong, Caifu Chen, Alexander V Vlassov, Susan Magdaleno
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引用次数: 44

Abstract

RNA interference (RNAi) is a mechanism in which the introduction of small interfering RNAs (siRNAs) into a diverse range of organisms and cell types causes degradation of the complementary mRNA. Applications of RNAi include gene function and pathway analysis, target identification and validation, and therapeutics. There is a need to develop reliable and easy-to-use assays to evaluate siRNA delivery efficiency and distribution, study pathways, and stability of siRNAs in cells (posttransfection) and in animals (postinjection). We have leveraged the Applied Biosystems TaqMan-based stem-loop RT-PCR technology, originally developed for quantification of endogenous microRNAs in cells, to fulfill these needs. The application protocols developed enable robust quantification of siRNA, including chemically modified siRNA molecules, in vitro and in vivo.

体外和体内sirna的茎环RT-PCR定量。
RNA干扰(RNAi)是一种将小干扰RNA (sirna)引入多种生物体和细胞类型中导致互补mRNA降解的机制。RNAi的应用包括基因功能和通路分析、靶标识别和验证以及治疗学。需要开发可靠且易于使用的检测方法来评估siRNA在细胞(转染后)和动物(注射后)中的传递效率和分布、研究途径以及siRNA的稳定性。我们利用应用生物系统公司基于taqman的茎环RT-PCR技术来满足这些需求,该技术最初是为定量细胞内源性microrna而开发的。开发的应用程序协议能够在体外和体内对siRNA进行稳健的定量,包括化学修饰的siRNA分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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