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β-D-Galactosidase (EC 3.2.1.23) is an enzyme that hydrolyzes glycosidic bonds, and it is present in cells of various microorganisms, plants, and animals. β-D-Galactosidase was used as an enzyme, and o-nitrophenyl β-D-galactopyranoside (ONPG) and p-nitrophenyl β-D-galactopyranoside (PNPG) were used as competitive substrates. Reaction products of o-nitrophenol (ONP) and p-nitrophenol (ONP) were detected as plateau signals in the CE/DFA format. Two-steps plateau signal was detected with the mixed sample solution of ONPG and PNPG on the basis of the different electrophoretic mobility of the products. Michaelis-Menten analysis and inhibition analysis were made with the two-steps plateau signal. This service provides a method for the substrate competition by in-capillary reaction.