Lin P H, Selinfreund R, Wharton W
Methods Enzymol. 1991;198:251-9. doi: 10.1016/0076-6879(91)98026-3.
The cell membrane isolation procedure we developed here can be scaled up from four to several hundred plates of cultured cells. Transmission electron microscopy, membrane marker enzyme analysis, binding study, EGF-dependent receptor autophosphorylation, and Western blots all demonstrate the biological activity of the purified cell membranes. The membrane purification procedure has been adapted by others in assessing EGF kinase activity and has been used for the purification of cell membranes from other types of cultured cells.
我们在此开发的细胞膜分离程序可以从培养的四板细胞扩大到数百板细胞。透射电子显微镜、膜标记酶分析、结合研究、表皮生长因子(EGF)依赖性受体自身磷酸化以及蛋白质免疫印迹均证明了纯化细胞膜的生物活性。其他人已采用该膜纯化程序来评估EGF激酶活性,并且该程序已用于从其他类型的培养细胞中纯化细胞膜。