Khurana S, K M
Department of Zoology, University of Delhi, India.
Indian J Biochem Biophys. 1995 Oct;32(5):245-8.
Passive transfer of proteins from preparative polyacrylamide gels to nitrocellulose membrane (NTC) was investigated. The transfer was carried out without the removal of sodium dodecyl sulphate from the denaturing gels. The transfer was quick, easy to perform, and does not require any apparatus. More than one replica of the same band can be obtained by successive transfer to more than one NTC without significantly affecting the Coomassie Brilliant Blue (CBB) staining ability of protein bands left in the gel. A fraction of protein transferred passively in the absence of electrical current from as low as 1.5 micrograms of protein per band in a 2 mm thick gel was found sufficient for detection with amido black staining, and more so by immunostaining. The method was found highly satisfactory for seven proteins (14 kDa to 66 kDa) checked in the present study and can be adopted, after checking its efficacy for any protein, for routine qualitative tests.
研究了蛋白质从制备型聚丙烯酰胺凝胶到硝酸纤维素膜(NTC)的被动转移。转移过程中未从变性凝胶中去除十二烷基硫酸钠。这种转移快速、易于操作,且不需要任何仪器。通过连续转移到多个NTC上,可以获得同一蛋白条带的多个复制品,而不会显著影响留在凝胶中的蛋白条带的考马斯亮蓝(CBB)染色能力。发现在2mm厚的凝胶中,每带低至1.5微克蛋白质在无电流情况下被动转移的一部分蛋白质足以用氨基黑染色检测,免疫染色检测效果更佳。在本研究中检测的七种蛋白质(14 kDa至66 kDa)中,该方法被发现非常令人满意,在检查其对任何蛋白质的有效性后,可用于常规定性试验。