论文部分内容阅读
Abstract A DNA fragment encoding C-terminal BARc region (128-416 AAs) in PICK1 was inserted into a modified vector pMAL-s involving a PreScission Protease (PPase) cleavage site to form a recombinant plasmid,pMAL-s-barc.The construct can express the fusion product MBP-BARc in the soluble form in E.coli.