Love James D
Department of Biochemistry, Albert Einstein College of Medicine at Yeshiva University, Bronx, NY, USA.
ATUM, 37950 Central Court, Newark, CA, 94560, USA.
Methods Mol Biol. 2017;1586:265-278. doi: 10.1007/978-1-4939-6887-9_17.
Production of prokaryotic membrane proteins for structural and functional studies in E. coli can be parallelized and miniaturized. All stages from cloning, expression, purification to detergent selection can be investigated using high-throughput techniques to rapidly and economically find tractable targets.
在大肠杆菌中生产用于结构和功能研究的原核膜蛋白可以实现并行化和小型化。从克隆、表达、纯化到去污剂选择的所有阶段都可以使用高通量技术进行研究,以快速、经济地找到易于处理的目标。