Dutta C, Henry H L
Department of Biochemistry, University of California, Riverside 92521.
Anal Biochem. 1990 Jan;184(1):96-9. doi: 10.1016/0003-2697(90)90018-5.
The feasibility of detecting hemoproteins after electroblotting was examined. Hemoproteins were subjected to lithium dodecyl sulfate-polyacrylamide gel electrophoresis (LDS-PAGE) and then electroblotted and peroxidase activity was detected with 3,3',5,5'-tetramethylbenzidine The sensitivity and specificity of tetramethylbenzidine staining of LDS-PAGE gels was retained when proteins were electroblotted. Subsequent staining of the membrane with Coomassie blue R-250 revealed a protein pattern similar to that in the polyacrylamide gel. Thus electroblotting of hemoproteins does not affect resolution of the electrophoretic pattern and heme-associated peroxidase activity. Additionally, the ability to stain hemoproteins on polyvinylidene difluoride membranes offers the advantage of utilizing the same membrane for further biochemical and immunological characterizations.
研究了电转印后检测血蛋白的可行性。将血蛋白进行十二烷基硫酸锂-聚丙烯酰胺凝胶电泳(LDS-PAGE),然后进行电转印,并用3,3',5,5'-四甲基联苯胺检测过氧化物酶活性。当蛋白质进行电转印时,LDS-PAGE凝胶的四甲基联苯胺染色的灵敏度和特异性得以保留。随后用考马斯亮蓝R-250对膜进行染色,显示出与聚丙烯酰胺凝胶中相似的蛋白条带模式。因此,血蛋白的电转印不会影响电泳图谱的分辨率和与血红素相关的过氧化物酶活性。此外,在聚偏二氟乙烯膜上对血蛋白进行染色的能力为利用同一膜进行进一步的生化和免疫学特性分析提供了优势。