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全转录组 RNA(包括非编码 RNA)的微阵列分析。

Microarray Analysis of Whole-Transcriptome RNAs Including Non-Coding RNAs.

机构信息

Université de Lorraine, CNRS, IMoPA, Nancy, France.

出版信息

Methods Mol Biol. 2021;2300:143-164. doi: 10.1007/978-1-0716-1386-3_14.

Abstract

Non-coding RNAs participate in most cellular processes and play a causative role in several diseases. In addition to their relevance as targets or tools for therapy, ncRNAs have been extensively detected in body fluids supporting their role as easily accessible and minimally invasive biomarkers. However, the precise measurement of circulating ncRNAs remains challenging due to their low abundance and the heterogeneity of the ncRNA population (size, polyadenylation status, circular forms). Microarrays constitute a very powerful method to analyze the expression level and the splicing pattern of circulating ncRNAs since they preserve sample integrity (no need to remove globin or rRNA) and allow precise quantification of low-abundance transcripts (no limitation by read depth). This chapter describes the protocols used in our lab to extract and purify total RNAs from PAXgene RNA Blood Tubes and to perform RNA labeling and hybridization on the Clariom™ D microarrays from Affymetrix.

摘要

非编码 RNA 参与大多数细胞过程,并在多种疾病中起因果作用。除了作为治疗靶点或工具的相关性外,ncRNA 还在体液中广泛检测到,支持其作为易于获取和微创的生物标志物的作用。然而,由于其丰度低和 ncRNA 群体的异质性(大小、多聚腺苷酸化状态、环形形式),精确测量循环 ncRNA 仍然具有挑战性。微阵列是分析循环 ncRNA 的表达水平和剪接模式的非常强大的方法,因为它们保留了样品的完整性(不需要去除球蛋白或 rRNA),并允许对低丰度转录物进行精确定量(不受读取深度的限制)。本章描述了我们实验室从 PAXgene RNA Blood Tubes 中提取和纯化总 RNA 以及在 Affymetrix 的 Clariom™ D 微阵列上进行 RNA 标记和杂交的方案。

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