孕妇血清中早孕因子的分离与纯化
血清早孕因子,,孕妇;,血清早孕因子;,分离纯化;,分子量,1材料与方法,2结果,3讨论,参考文献:
摘要: 目的:建立一条从妊娠早期妇女血清中分离纯化早孕因子的技术路线,获得高纯度的早孕因子。方法:采用依次经过DEAE 52阴离子交换层析、SP Sepharose F.F阳离子交换层析、ConA Sepharose 4B亲和层析和Heparin Sepharose Cl6B亲和层析分离纯化的方案,最终得到具有早孕因子活性的HeparinⅡ成分,早孕因子活性采用活性玫瑰花环抑制实验检测。采用SDS聚丙烯酰胺凝胶电泳鉴定纯化物。结果:SDS聚丙烯酰胺凝胶电泳结果显示有一条电泳区带,相对分子量为10.91 kDa。结论:这条分离纯化早孕因子的技术路线是可行的,得到的相对分子量为10.91 kDa的蛋白质为电泳纯的早孕因子。关键词:孕妇; 血清早孕因子; 分离纯化; 分子量
Isolation and purification of Early Pregnancy Factor from Human Pregnancy Sera
LIU Xiaoyu, SUN Wendong, YUAN Wumei, et al
(Department of Biochemistry and Molecular Biology, Xinjiang Medical University,Urumqi 830054,China)
Abstract: Objective: Set up a method of isolation and purification of early pregnancy factor(EPF) from human pregnancy sera, and get pure EPF. Methods: The purification scheme involved sequential DEAE 52 chromatography, SP Sepharose F.F chromatography, ConA Sepharose 4B chromatography and Heparin Sepharose Cl6B chromatography. The biological activity was detected by rosette inhibition test. It was Identified by sodium dodecyl sulfatepolyacrylamide gel electrophoresis (SDSPAGE). Result: One band was observed on SDSPAGE profile, and the molecular weight was 10.91 kDa. Conclusion: This method is advisable. The purified protein has a molecular mass of 10.91 kDa as analyzed by SDSPAGE, which is similar to the report of Cavanagh AC. ......
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