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小非编码RNA的荧光原位杂交

Fluorescence in situ hybridization of small non-coding RNAs.

作者信息

Vautrot Valentin, Aigueperse Christelle, Branlant Christiane, Behm-Ansmant Isabelle

机构信息

CNRS, UMR 7365 IMoPA, Université de Lorraine, 9 avenue de la Forêt de Haye, Vandoeuvre-lès-Nancy, 54506, France.

出版信息

Methods Mol Biol. 2015;1296:73-83. doi: 10.1007/978-1-4939-2547-6_8.

Abstract

RNA FISH is a powerful method to detect specific RNAs in fixed cells. It allows both localization and quantification of RNA molecules within individual cells and tissues. Refined RNA FISH methods have also been developed to determine RNA transcription and degradation rates. This chapter describes an RNA FISH protocol that we developed in order to study the expression and localization of satellite III RNAs. This specific class of non-coding RNAs is expressed in response to various cellular stresses including heat shock. This protocol is based on the use of a biotinylated LNA probe subsequently detected by a streptavidin-Alexa Fluor(®) 488 conjugate. A protocol allowing efficient coupling of RNA FISH and protein detection by immunofluorescence is also described in this chapter.

摘要

RNA荧光原位杂交(RNA FISH)是一种在固定细胞中检测特定RNA的强大方法。它能够对单个细胞和组织内的RNA分子进行定位和定量分析。人们还开发了精细的RNA FISH方法来测定RNA转录和降解速率。本章介绍了我们为研究卫星III RNA的表达和定位而开发的一种RNA FISH方案。这类特定的非编码RNA在包括热休克在内的各种细胞应激反应中表达。该方案基于使用生物素化的锁核酸(LNA)探针,随后用链霉亲和素- Alexa Fluor(®)488共轭物进行检测。本章还描述了一种能有效将RNA FISH与免疫荧光蛋白检测相结合的方案。

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