Quantitation of protein on gels and blots by infrared fluorescence of Coornassie blue and Fast Green

被引:89
作者
Luo, S [1 ]
Wehr, NB [1 ]
Levine, RL [1 ]
机构
[1] NHLBI, Biochem Lab, Bethesda, MD 20892 USA
关键词
Coomassie blue; protein quantitation; infrared fluorescence; Fast Green;
D O I
10.1016/j.ab.2005.10.048
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Coomassie blue staining of gels and blots is commonly employed for detection and quantitation of proteins by densitometry. We found that Coomassie blue or Fast Green FCF bound to protein fluoresces in the near infrared. We took advantage of this property to develop a rapid and sensitive method for detection and quantitation of proteins in gels and oil blots. The fluorescence response is quantitative for protein content between 10 ng and 20 mu g per band or spot. Staining and destaining require only 30 min, and the method is compatible with subsequent immunodetection. Published by Elsevier Inc.
引用
收藏
页码:233 / 238
页数:6
相关论文
共 13 条
[11]   ENZYMIC PROCEDURES FOR DETERMINING THE AVERAGE STATE OF ADENYLYLATION OF ESCHERICHIA-COLI GLUTAMINE-SYNTHETASE [J].
STADTMAN, ER ;
SMYRNIOTIS, PZ ;
DAVIS, JN ;
WITTENBERGER, ME .
ANALYTICAL BIOCHEMISTRY, 1979, 95 (01) :275-285
[12]   IMMUNOBLOTTING AND DOT IMMUNOBINDING - CURRENT STATUS AND OUTLOOK [J].
TOWBIN, H ;
GORDON, J .
JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 72 (02) :313-340
[13]  
WILSON CM, 1983, METHOD ENZYMOL, V91, P236