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cDNA末端快速扩增技术的革命:用于全长cDNA末端聚合酶链反应克隆的新策略

Revolutions in rapid amplification of cDNA ends: new strategies for polymerase chain reaction cloning of full-length cDNA ends.

作者信息

Schaefer B C

机构信息

Division of Tumor Virology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.

出版信息

Anal Biochem. 1995 May 20;227(2):255-73. doi: 10.1006/abio.1995.1279.

Abstract

Rapid amplification of cDNA ends (RACE) is a polymerase chain reaction (PCR)-based technique which was developed to facilitate the cloning of full-length cDNA 5'- and 3'-ends after a partial cDNA sequence has been obtained by other methods. While RACE can yield complete sequences of cDNA ends in only a few days, the RACE procedure frequently results in the exclusive amplification of truncated cDNA ends, undermining efforts to generate full-length clones. Many investigators have suggested modifications to the RACE protocol to improve the effectiveness of the technique. Based on first-hand experience with RACE, a critical review of numerous published variations of the key steps in the RACE method is presented. Also included is a detailed, effective protocol based on RNA ligase-mediated RACE/reverse ligation-mediated PCR, as well as a demonstration of its utility.

摘要

cDNA末端快速扩增(RACE)是一种基于聚合酶链反应(PCR)的技术,它是在通过其他方法获得部分cDNA序列后,用于促进全长cDNA 5'端和3'端的克隆。虽然RACE仅需几天就能产生cDNA末端的完整序列,但RACE程序经常导致截短的cDNA末端的特异性扩增,破坏了生成全长克隆的努力。许多研究者建议对RACE方案进行修改以提高该技术的有效性。基于RACE的第一手经验,本文对RACE方法关键步骤的众多已发表变体进行了批判性综述。还包括基于RNA连接酶介导的RACE/反向连接介导的PCR的详细有效方案及其效用的演示。

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