4.6 Article

A rapid DNA assembling strategy mediated by direct full-length polymerase chain reaction

期刊

GENE
卷 523, 期 2, 页码 122-125

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.gene.2013.03.140

关键词

Class-IIS endonuclease; Direct full-length polymerase chain reaction (PCR); DNA assembling; Ligation; Multiple site-directed mutagenesis

资金

  1. National Natural Science Foundation of China [30973878]
  2. Excellent Research Team Cultivation Program of Shanghai University of Traditional Chinese Medicine

向作者/读者索取更多资源

An efficient DNA assembling strategy was developed here modified from Class-IS endonuclease mediated DNA splicing by directed ligation (SDL). Benefited from the full-length PCR directly using ligation products as template, this strategy required less effort and less time to obtain the assembled full-length DNA. The advantages of this strategy made it a rapid and easy-to-perform gene splicing and multiple site-directed mutagenesis approach especially practicable when more fragments need to be assembled at the same time. (C) 2013 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据