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- W1992806688 abstract "1. A sensitive radioactive method is described for the determination of xanthine oxidase activity. 2. [8-14C] xanthine is incubated with the enzyme in phosphate buffer pH 7.4 at 37° for 3 h. The reaction is stopped with TCA and the protein-free filtrate is passed through a Dowex 50 column. The xanthine is quantitatively adsorbed to the resin and the uric acid is entirely recovered in the first 10 ml of 0.1 N HCl eluate and is counted. The method is calibrated against purified xanthine oxidase assayed spectrophotometrically. 3. The method is able to measure 2.10−7 and is linear up to 5.10−5 international units of xanthine oxidase and is therefore more sensitive than the standard assays by 3–4 orders of magnitude. 4. The method has been successfully used for the assay of the enzyme in serum, whole blood and tissue extracts." @default.
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- W1992806688 date "1965-01-01" @default.
- W1992806688 modified "2023-09-23" @default.
- W1992806688 title "A sensitive method for the determination of xanthine oxidase activity" @default.
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- W1992806688 doi "https://doi.org/10.1016/0009-8981(65)90091-4" @default.
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