Gella F J, Olivella M T, Pegueroles F, Gener J
Clin Chem. 1981 Oct;27(10):1686-9.
We describe a procedure for assay of diaphorase activity in commercial purified preparations and in clinical chemical reagents by use of iodonitrotetrazolium chloride or other tetrazolium salts. The method is based on measurement of the formazan produced by enzymic reduction of tetrazolium salts in the presence of NADH. The assay procedure has been optimized for linear kinetics, simplicity of operation, nondetectable blank rates, and extended activity/enzyme concentration proportionality. The proposed method has several advantages over the older assay by use of dichlorophenolindophenol.
我们描述了一种通过使用氯化碘硝基四氮唑蓝或其他四氮唑盐来测定商业纯化制剂和临床化学试剂中黄递酶活性的方法。该方法基于在NADH存在下,通过酶促还原四氮唑盐产生的甲臜的测量。该测定程序已针对线性动力学、操作简单性、不可检测的空白率以及扩展的活性/酶浓度比例进行了优化。与使用二氯酚靛酚的旧方法相比,所提出的方法具有几个优点。