DNA staining in agarose and polyacrylamide gels by methyl green

被引:1
作者
Murgai, P. [1 ]
Sharma, P. [1 ]
Sachdeva, M. U. S. [1 ]
Das, R. [1 ]
Varma, N. [1 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Hematol, Level 5,Res Block ASect 12, Chandigarh 160012, India
关键词
DNA binding; ethidium bromide; far red fluorescence; gel documentation system; intercalating agent; methyl green; molecular biology; Serva DNA stain G (TM); BINDING;
D O I
10.1080/10520295.2018.1511062
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Methyl green (MG) is an inexpensive, nonproprietary, traditional histological stain for cell nuclei. When bound to DNA and upon excitation with orange-red light, it fluoresces brightly in the far red region. We compared MG with ethidium bromide (EtBr), the conventional stain for DNA in gels, and Serva DNA stain G (TM) (SDsG), a proprietary stain marketed as a safer alternative to EtBr for staining of electrophoresed DNA bands in agarose and polyacrylamide gels. DNA-MG fluorescence was recorded and 2.4 mu g/ml MG produced crisp images of electrophoresed DNA after incubation for 10 min. Stain solutions were stable and detection limits for faint bands as well as relative densitometric quantitation were equivalent to EtBr. MG, EtBr and SDsG cost 0.0192, 0.024 and 157.5 US cents/test, respectively. MG is an effective stain for visualizing DNA in agarose and polyacrylamide gels. Its major advantages including low cost, comparable quality of staining, storage at room temperature, photo-resistance and low mutagenic profile outweigh its disadvantages such as staining of tracking dye and requirement for a gel documentation system with a red filter.
引用
收藏
页码:581 / 588
页数:8
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