Biochemistry, University of KwaZulu-Natal, Pietermaritzburg, South Africa.
Biochemistry, University of KwaZulu-Natal, Pietermaritzburg, South Africa.
Anal Biochem. 2019 Feb 1;566:107-115. doi: 10.1016/j.ab.2018.11.015. Epub 2018 Nov 17.
Coomassie brilliant blue R250, an anionic dye is the most popular stain to detect proteins resolved in SDS-PAGE gels. Crystal violet, a cationic dye was found to be versatile and stained proteins in SDS-PAGE gels and in zymograms. Stained proteins can be transferred to nitrocellulose and the stained proteins on the western detected with enzyme coupled antibodies. Staining can be reversed. Staining takes 3 h at RT or 30 min at 60 °C. Crystal violet stained some E. coli high and low molecular weight proteins not stained by Coomassie blue R250. Crystal violet stained down to 16 ng of protein, some five-fold lower than Coomassie blue, though the two stains had a similar linear dynamic range. The staining sensitivity could be increased to 2 ng when crystal violet and Coomassie blue were combined in a double staining/counterion dye formulation. The low concentrations of the dye without a destaining step reduces the costs of the technique and results in a more environmentally friendly stain compared to traditional staining methods.
考马斯亮蓝 R250 是一种阴离子染料,是检测 SDS-PAGE 凝胶中蛋白质的最常用的染色剂。阳离子染料结晶紫被发现具有多功能性,可以染色 SDS-PAGE 凝胶和同工酶中的蛋白质。染色后的蛋白质可以转移到硝酸纤维素上,并用酶偶联抗体检测到蛋白质印迹上的染色蛋白。染色可以逆转。染色可以在室温下进行 3 小时,或在 60°C 下进行 30 分钟。结晶紫可以染色一些大肠杆菌的高分子量和低分子量蛋白,而考马斯亮蓝 R250 不能染色这些蛋白。结晶紫可以染色低至 16ng 的蛋白质,比考马斯亮蓝低五倍,但两种染色剂具有相似的线性动态范围。当结晶紫和考马斯亮蓝在双染色/抗衡离子染料配方中组合使用时,染色灵敏度可以提高到 2ng。这种低浓度的染料无需脱色步骤,降低了技术成本,与传统染色方法相比,产生的染色更环保。