Brilliant Blue G is used in analytical biochemistry dye and as a P2X7 antagonist. It is also used in protein staining following gel electrophoresis. It is used to prepare the protein reagent for the determination of protein content of the collagenase enzyme isolated from fish waste. It may be employed as stain for the internal limiting membrane (ILM) for the macular hole (MH) and epiretinal membrane (ERM) surgery. It is useful for SDS gels as it readily stains proteins with minimal background color. Protein bands can be visualized during staining. It has been used in the Bradford dye-binding protein assay. A mechanism for dye binding to protein has been proposed, based on measuring Coomassie Brilliant Blue G-250 (CBBG) absorbance spectra during titration of the dye reagent in the absence of protein and its response to different polyamino acids. Brilliant Blue G has been used for determining critical micelle concentration of detergents.
Hiroshi Enaida.; Toshio Hisatomi.; Yasuaki Hata.; Akifumi Ueno.; Yoshinobu Goto.; Tomomi Yamada.; Toshiaki Kubota.; Tatsuro Ishibashi. Brilliant blue G selectively stains the internal limiting membrane/brilliant blue G-assisted membrane peeling. Retina. 2006, 26, (6), 631-636.
John Pierce.; C.H. Suelter. An evaluation of the Coomassie brilliant blue G-250 dye-binding method for quantitative protein determination. Analytical Biochemistry. 1977, 81 (2), 478-480.
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