摘要
参照1993年Frimpong等表达仓鼠同源酶催化域的研究结果,将PCR法制备的人HMG-CoA还原酶催化域cDNA克隆入表达载体pET30,使表达产物C端融合载体编码的His-Tag,以利产物的稳定和完整产物的纯化。
In respect that the expression of Syrian Hamster HMG-CoA reductase with C-terminal EEF extension produce homogeneous protein with high catalytic activity reported by Frimpong et al in 1993, human HMG-CoA reductase cDNA prepared by PCR is inserted into expression vector PET30, so that the product will carry C-terminal fusion His-Tag for production of homogeneous protein and purification of intact product.
出处
《高技术通讯》
EI
CAS
CSCD
1997年第2期50-52,共3页
Chinese High Technology Letters
基金
国家自然科学基金
863计划