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[噬菌体M13中的一种简单克隆系统及使用终止子的DNA测序]

[A simple system of cloning in phage M13 and DNA sequencing with terminators].

作者信息

Kraev A S

出版信息

Mol Biol (Mosk). 1988 Sep-Oct;22(5):1164-97.

PMID:3065614
Abstract

A compilation of techniques for DNA cloning in filamentous phage M13 based vectors for a novice in cloning is presented. It does not require either specialized microbiological facilities, or any specific knowledge in Escherichia coli genetics. The cloning strategy uses only blunt-end ligation into a vector that has been prepared once for several hundred experiments. The first part describes the isolation, preparation and checking of a blunt-ended M13 vector (with M13 mp series vectors as an example), and also the isolation of clonable fragments, transformation of competent cells and preliminary analysis of recombinants. The second part describes procedures and equipment, which enable to sequence recombinant M13 clones by the chain termination procedure of Sanger et al. It includes simplified procedures for the preparation of sequencing gels, and the rules of interpretation of the sequencing ladders. Reference material is added, which includes trouble-shooting guide, E. coli K12 strain list and polylinker sequences for use of mp-series vectors as well as a fully documented cloning and sequencing experiment.

摘要

本文为克隆新手介绍了基于丝状噬菌体M13载体的DNA克隆技术汇编。该技术既不需要专门的微生物学设施,也不需要大肠杆菌遗传学方面的任何特定知识。克隆策略仅使用平端连接到一个已制备好可用于数百次实验的载体中。第一部分描述了平端M13载体的分离、制备和检测(以M13 mp系列载体为例),以及可克隆片段的分离、感受态细胞的转化和重组体的初步分析。第二部分描述了通过桑格等人的链终止法对重组M13克隆进行测序的程序和设备。其中包括制备测序凝胶的简化程序以及测序梯的解读规则。此外还添加了参考资料,包括故障排除指南、大肠杆菌K12菌株列表、用于mp系列载体的多克隆位点序列,以及一个有完整记录的克隆和测序实验。

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