Jung D W, Yoo G S, Choi J K
College of Pharmacy, Chonnam National University, Kwangju, Korea.
Electrophoresis. 1998 Oct;19(14):2412-5. doi: 10.1002/elps.1150191409.
We have developed a new mixed-dye protein staining method that is simple, rapid, and sensitive. A freshly prepared mixture of calconcarboxylic acid (NN, 0.02%) and rhodamine B (RB, 0.04%) in 40% methanol/7% acetic acid, was used as a staining solution. RB acts as an auxiliary agent to inhibit the binding of NN to the gel matrix, reducing the background staining and therefore enhancing the protein staining by NN. This mixed-dye staining method reduces the total staining and destaining time to less than an hour, and increases the sensitivity to 25 ng of bovine serum albumin, which is greater than the 100 ng sensitivity limit of Coomassie Brilliant Blue R-250 (CBBR) staining.
我们开发了一种新的混合染料蛋白质染色方法,该方法简单、快速且灵敏。将钙黄绿素(NN,0.02%)和罗丹明B(RB,0.04%)在40%甲醇/7%乙酸中新鲜配制的混合物用作染色溶液。RB作为辅助剂,可抑制NN与凝胶基质的结合,减少背景染色,从而增强NN对蛋白质的染色效果。这种混合染料染色方法将总染色和脱色时间缩短至不到一小时,并将灵敏度提高到25 ng牛血清白蛋白,高于考马斯亮蓝R-250(CBBR)染色的100 ng灵敏度极限。