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用俾斯麦棕R对聚丙烯酰胺凝胶中的蛋白质进行改良考马斯亮蓝染色。

A modified Coomassie blue staining of proteins in polyacrylamide gels with Bismark brown R.

作者信息

Choi J K, Yoon S H, Hong H Y, Choi D K, Yoo G S

机构信息

College of Pharmacy, Chonnam National University, Kwangju, 500-757, Korea.

出版信息

Anal Biochem. 1996 Apr 5;236(1):82-4. doi: 10.1006/abio.1996.0134.

Abstract

A rapid and sensitive protein staining method employing a mixed dye technique has been developed. Solutions of Coomassie brilliant blue R-250 (CB, 0.2%) and Bismark brown R (BBR, 0.05%) were mixed in the volume ratio of 1:0.75 for staining (final molar ratio, 4.5:1). In this staining, BBR inhibits the binding of CB to gel matrix by forming ion-pairing complex with excess CB; therefore, it reduces staining/destaining times and also enhances the staining effect of CB on protein band. As a result, the mixed dye staining enables complete staining/destaining within 20/25 min and detection of up to 25 ng of bovine serum albumin.

摘要

已开发出一种采用混合染料技术的快速灵敏蛋白质染色方法。将考马斯亮蓝R - 250(CB,0.2%)溶液和俾斯麦棕R(BBR,0.05%)溶液按1:0.75的体积比混合用于染色(最终摩尔比为4.5:1)。在这种染色中,BBR通过与过量的CB形成离子对复合物来抑制CB与凝胶基质的结合;因此,它缩短了染色/脱色时间,还增强了CB对蛋白条带的染色效果。结果,混合染料染色能够在20/25分钟内完成完全染色/脱色,并能检测到多达25 ng的牛血清白蛋白。

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