作者
Mark R Slaughter, Peter J O’Brien
发表日期
2000/10/31
期刊
Clinical Biochemistry
卷号
33
期号
7
页码范围
525-534
出版商
Elsevier
简介
Objectives
Develop fully automated assay of antioxidant catalatic activity of catalase.
Design and methods
The assay is based on standard, clinical chemistry automated analyzer methods for measuring hydrogen peroxide by using the Trinder reagent. Catalase competes with 324 U/L horseradish peroxidase (type XII) and Trinder reagent for hydrogen peroxide produced by 46 U/L uricase action on urate. Unit activity is defined as 50% inhibition of maximal color development.
Results
Within-run coefficients of variation (cv) were 2% for standards and samples, whereas between-run cv was 3.1% for standards and 7.3% for samples. Dilutional parallelism and linearity were demonstrated for 8-fold dilutions of samples over the range 0.1 to 1.1 U/mL. Recovery of added catalase was complete. Samples are stable to freezing and storage for 1 week at −80 °C. Activities (units/mL) ranged from 0.29 to 0.41 in human and …
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