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出 处:《生物化学与生物物理学报》1994年第4期351-356,共6页
基 金:国家自然科学基金
摘 要:GD3合成酶(CMP-NeuAc:GM3唾液酸转移酶,ST2)是膜嵌合蛋白,定位于高尔基体。经过制作微粒体、Triton增溶、AH-Sepharose及GM3-Glassbeads亲和层析等步骤,二乙基亚硝胺诱发大鼠肝癌组织中的ST2被纯化了31597倍,得率为0.35%。SDS-聚丙烯酰胺凝胶电泳后银染色呈1条蛋白着色带,分子量为55kd.GD3 synthetase(ST2)is a membrane protein localized in the Golgi body.This paper reported its purification to homogeneity on SDS-PAGE. Liver cancer tissue from diethylnitrosamine-induced rat was homogenized and centrifuged.The membrane precipitation was solubilized with 1% Triton X-100/Triton CF-54(W/W1:1). After aminohexyl-Sepharose and GM3-Glassbeads affinity chromatography, the enzyme was purified by 31597 times. Its yield was 0.35%.Thepurified product gave one band on SDS-PAGE with silver staining with a MW of55kd.
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