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用于克隆的限制性内切酶识别位点的化学合成

Chemical synthesis of restriction enzyme recognition sites useful for cloning.

作者信息

Scheller R H, Dickerson R E, Boyer H W, Riggs A D, Itakura K

出版信息

Science. 1977 Apr 8;196(4286):177-80. doi: 10.1126/science.847463.

Abstract

By a triester chemical synthesis method, three decameric DNA's have been made; these act as substrates for several restriction endonucleases, including Eco RI, Bam I, and Hind III. These homogenous decamers form duplexes that can be efficiently blunt-end ligated to themselves or to other DNA molecules by the action of T4 DNA ligase and thus are useful tools for molecular cloning experiments.

摘要

通过三酯化学合成法制备了三种十聚体DNA;它们可作为几种限制性内切酶的底物,包括Eco RI、Bam I和Hind III。这些均一的十聚体形成双链体,通过T4 DNA连接酶的作用可有效地自身平端连接或与其他DNA分子平端连接,因此是分子克隆实验的有用工具。

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