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测定肝脏总RNA中单个mRNA种类的聚腺苷酸尾长度。

Determination of the poly(A) tail lengths of a single mRNA species in total hepatic RNA.

作者信息

Zangar R C, Hernandez M, Kocarek T A, Novak R F

机构信息

Institute of Chemical Toxicology, Wayne State University, Detroit, MI 48201, USA.

出版信息

Biotechniques. 1995 Mar;18(3):465-9.

PMID:7779397
Abstract

Poly(A) tail length is important in the stability and translation of mRNA. We describe procedures for the rapid and reproducible analysis of poly(A) tail length of a single mRNA species contained in a sample of total hepatic RNA. A short 3' fragment of a specific mRNA is prepared by RNase H digestion of the targeted mRNA region annealed to a short DNA oligonucleotide. The length of the poly(A) tail of the 3' fragment is then determined by running the sample on a polyacrylamide gel, by electrophoretic transfer, by probing with a radiolabeled cDNA and by comparing the size of the detected region with a specific RNA ladder or a DNA ladder.

摘要

聚腺苷酸(Poly(A))尾长度对信使核糖核酸(mRNA)的稳定性和翻译很重要。我们描述了快速且可重复地分析总肝RNA样本中单个mRNA种类的聚腺苷酸尾长度的方法。通过核糖核酸酶H(RNase H)消化与短DNA寡核苷酸退火的靶向mRNA区域,制备特定mRNA的短3'片段。然后通过将样品在聚丙烯酰胺凝胶上进行电泳、电泳转移、用放射性标记的互补脱氧核糖核酸(cDNA)进行探针检测以及将检测区域的大小与特定RNA梯尺或DNA梯尺进行比较,来确定3'片段的聚腺苷酸尾长度。

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