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以5'-单磷酸肌苷为底物连续测定血清5-核苷酸酶活性,并使用转移分析仪(Kem-O-Mat)实现完全自动化。

Continuous assay of serum 5-nucleotidase activity with inosine 5'-monophosphate as substrate and total automation using a transfer-analyzer (Kem-O-Mat).

作者信息

Stephant E, Vernet-Nyssen M, Mousson B

出版信息

J Clin Chem Clin Biochem. 1983 Aug;21(8):481-9. doi: 10.1515/cclm.1983.21.8.481.

Abstract

The continuous spectrophotometric assay of 5'-nucleotidase originally described by Heinz et al. ((1980) J. Clin. Chem. Clin. Biochem. 18, 781-788) was modified and fully automated on a Kem-O-Mat transfer analyzer, using inosine 5'-monophosphate as substrate. The reaction product was hydrogen peroxide and the reduction of NADP was observed for 10 minutes at 340 nm and at a reaction temperature of 30 degrees C. The different factors involved in the enzyme reaction were checked, including the substrate concentration, reaction rate, linearity and substrate preservation. Normal values ranged from 1 to 13 U/l. Between-day reproducibility was estimated with two different commercial control sera, and the coefficient of variation was 5% for the upper limit of normal activity (23 U/l). There was good agreement between the present method and a semi-automatic colorimetric technique (for 100 sera tested by both methods, the correlation coefficient was 0.974 and the regression line equation, y = 0.85 x- 1.5). Despite the lengthy reagent mixture preparation procedure, the method permitted assay of 50 samples per hour. The occurrence of high serum blanks in certain pathological states is discussed.

摘要

最初由海因茨等人描述的((1980)《临床化学与临床生物化学杂志》18卷,781 - 788页)5'-核苷酸酶连续分光光度测定法进行了改进,并在Kem - O - Mat转移分析仪上实现了完全自动化,使用5'-单磷酸肌苷作为底物。反应产物是过氧化氢,在340nm波长和30℃反应温度下观察NADP的还原反应10分钟。检查了酶反应中涉及的不同因素,包括底物浓度、反应速率、线性和底物保存情况。正常范围为1至13U/L。使用两种不同的商业对照血清评估日间重复性,正常活性上限(23U/L)的变异系数为5%。本方法与半自动比色技术之间具有良好的一致性(两种方法均检测了100份血清,相关系数为0.974,回归线方程为y = 0.85x - 1.5)。尽管试剂混合物制备过程冗长,但该方法每小时可检测50个样本。讨论了某些病理状态下高血清空白的出现情况。

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