Salerno John C, Jones Rachel J, Erdogan Eda, Smith Susan M E
Biology Department, Rensselaer Polytechnic Institute, Science Center, 1W14, 110 8th St., Troy, NY 12180, USA.
Mol Biotechnol. 2005 Mar;29(3):225-32. doi: 10.1385/MB:29:3:225.
A single-stage polymerase-based procedure is described that allows extensive modifications of DNA. The version described here uses the QuikChange Site-Directed Mutagenesis System kit supplied by Stratagene. The original protocol is replaced by a single-stage method in which linear production of complementary strands is accomplished in separate single primer reactions. This has proved effective in introducing insertions and deletions into large gene/vector combinations without subcloning.
本文描述了一种基于聚合酶的单步程序,该程序可对DNA进行广泛修饰。这里所描述的版本使用的是Stratagene公司提供的QuikChange定点诱变系统试剂盒。原来的方案被一种单步方法所取代,在该方法中,互补链的线性合成是在单独的单引物反应中完成的。事实证明,这种方法在不进行亚克隆的情况下,将插入和缺失引入大型基因/载体组合中非常有效。