Yang Y, Jung D W, Bai D G, Yoo G S, Choi J K
College of Pharmacy, Chonnam National University, Kwangju, Korea.
Electrophoresis. 2001 Mar;22(5):855-9. doi: 10.1002/1522-2683()22:5<855::AID-ELPS855>3.0.CO;2-Y.
Sensitive and safe methods for visualization of DNA in agarose gels are described. 0.001% crystal violet dissolved in distilled water was used for DNA staining on agarose gels and it could detect as little as 16 ng of DNA (3 kb, pGem-7Zf/EcoRI) without destaining procedure. The detection limit is four times lower than that of ethidium bromide. To improve the sensitivity, we studied a counterion-dye staining method using methyl orange as a counterion-dye which contributes to reduce excessive background staining by crystal violet. Dye concentration, pH of staining solution, mixing molar ratio of two dyes, and staining times were optimized for the counterion-dye staining. By the staining with a mixed solution of 0.0025% crystal violet and 0.0005% methyl orange in distilled water, 8 ng of the 3 kb DNA in an agarose gel was detected within 30 min.
本文描述了用于在琼脂糖凝胶中可视化DNA的灵敏且安全的方法。将0.001%的结晶紫溶解于蒸馏水中用于琼脂糖凝胶上的DNA染色,它能够检测低至16 ng的DNA(3 kb,pGem-7Zf/EcoRI),无需脱色步骤。检测限比溴化乙锭低四倍。为提高灵敏度,我们研究了一种使用甲基橙作为抗衡离子染料的抗衡离子-染料染色方法,这有助于减少结晶紫过度的背景染色。对抗衡离子-染料染色的染料浓度、染色溶液的pH值、两种染料的混合摩尔比以及染色时间进行了优化。通过用0.0025%结晶紫和0.0005%甲基橙的混合溶液在蒸馏水中染色,在30分钟内检测到琼脂糖凝胶中8 ng的3 kb DNA。