摘要
目的对肌酸激酶(CK)同工酶进行纯化和重组。方法酶的制备和分子重组技术。结果纯化及重组后的CK-MM、CK-MB、CR-BB比活性分别为930000,692000,481000U·g-1(37℃);SDS-PAGE分析,CK-MM、CK-MB均呈现单带,而CK-BB为双带。
Objective To purify and recombine the creatine kinase(CK) isoenzyme. Methods\ Adopting purification and molecular recombinant techniques of enzyme. Results\ The specific activities of CK MM, MB and BB purified and recombined were 930 000 , 692 000 and 481 000 U·g -1 (37℃) respectively by SDS PAGE assay, both CK MM and MB showed single band, but CK BB showed double bands. Conclusions\ These results provide the basis for further investigation of preparation and immunoassay of CK MB monoclone antibody.
出处
《安徽医科大学学报》
CAS
1998年第6期413-415,共3页
Acta Universitatis Medicinalis Anhui
基金
安徽省卫生厅资助
关键词
肌酸激酶
同工酶
分离
提纯
重组
creatine kinase isoenzymes/isol
pectoralis muscles/enzymol
brain/enzymol
dogs