Gallati H
J Clin Chem Clin Biochem. 1977 Dec;15(12):699-703.
Most of the currently used enzyme-immunological tests employ horse radish peroxidase as a marker enzyme. A new method is described for the determination of extremely small quantities of peroxidase. This largely prevents the inactivation of the peroxidase by H2O2 and thereby permits a much longer incubation time. In the presence of 25 mmol/l phenol, 2 mmol/l 4-amino-antipyrin and 0.8 mmol/l H2O2, peroxidase catalyses the formation of a red quinonimine, whose increase in adsorption is directly proportional to the enzyme concentration.
目前大多数酶免疫检测采用辣根过氧化物酶作为标记酶。本文描述了一种测定极少量过氧化物酶的新方法。这在很大程度上防止了过氧化物酶被过氧化氢灭活,从而允许更长的孵育时间。在存在25 mmol/l苯酚、2 mmol/l 4-氨基安替比林和0.8 mmol/l过氧化氢的情况下,过氧化物酶催化形成红色醌亚胺,其吸光度的增加与酶浓度成正比。