大肠杆菌
重组DNA
蛋白质纯化
克隆(编程)
膜蛋白
合成生物学
生物
膜
同种类的
化学
计算生物学
生物化学
基因
计算机科学
物理
程序设计语言
热力学
作者
Benjamin McIlwain,Ali A. Kermani
出处
期刊:Methods in molecular biology
日期:2020-01-01
卷期号:: 13-27
被引量:6
标识
DOI:10.1007/978-1-0716-0373-4_2
摘要
Escherichia coli is the workhorse of the structural biology lab. In addition to routine cloning and molecular biology, E. coli can be used as a factory for the production of recombinant membrane proteins. Purification of homogeneous samples of membrane protein expressed in E. coli is a significant bottleneck for researchers, and the protocol we present here for the overexpression and purification of membrane proteins in E. coli will provide a solid basis to develop lab- and protein-specific protocols for your membrane protein of interest. We additionally provide extensive notes on the purification process, as well as the theory surrounding principles of purification.
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