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- W2333577771 abstract "This chapter presents a procedure for the preparation of glutathione peroxidase, which is regarded as a major protective system against endogenously and exogenously induced lipid peroxidation. Two types of methods are used for determining the activity of glutathione peroxidase. One involves a direct measurement of unconsumed glutathione (GSH) at fixed time periods by polarographic GSH analysis' (Method 1), or by the dithionitrobenzoic acid method (Method 2). The second approach takes advantage of the capability of glutathione reductase, with nicotinamide adenine dinucleotide phosphate (NADPH), to regenerate GSH from oxidized GSH. The decrease in NADPH is continuously measured spectrophotometrically, while the GSH concentration in the enzymatic cycle remains essentially constant (Method 3). A convenient source for the preparation of glutathione peroxidase is bovine blood including the following steps: hemolysate; organic solvent precipitation; phosphate precipitation; absorption to phenyl-sepharose; and washing on diethylaminoethyl (DEAE)–sephadex, S-300 sephacryl, and hydroxylapatite column." @default.
- W2333577771 created "2016-06-24" @default.
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- W2333577771 date "2011-08-01" @default.
- W2333577771 modified "2023-09-27" @default.
- W2333577771 title "Gender differences in susceptibility to carbon tetrachloride-induced hepatotoxicity in CD-1 mice" @default.
- W2333577771 doi "https://doi.org/10.1016/j.toxlet.2011.05.931" @default.
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