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用于尿液酶活性测定的质量控制物质。

Quality control material for activity determinations of urinary enzymes.

作者信息

Jung K, Grützmann K D

机构信息

Department of Experimental Organ Transplantation, University Hospital Charité, Humboldt University, Berlin, German Democratic Republic.

出版信息

Clin Biochem. 1988 Jan;21(1):53-7. doi: 10.1016/s0009-9120(88)80112-7.

Abstract

We examined the stability of N-acetyl-beta-D-glucosaminidase (EC 3.2.1.30), alanine aminopeptidase (EC 3.4.11.2), alkaline phosphatase (EC 3.1.3.1), gamma-glutamyltransferase (EC 2.3.2.2), and lysozyme (EC 3.2.1.17) in urine prepared by gel filtration and supplemented with albumin, or ethylene glycol, or ethylene glycol plus albumin during storage at -20 degrees C for a period of 12 months. The stability was assessed by linear regression analysis of monthly values versus time. All enzymes except for gamma-glutamyltransferase could be considered stable for about one year in all three control materials provided that maximum change of 10% of the starting enzyme activity is accepted as tolerable. If ethylene glycol is used as stabilizer, its suitability must be tested and its inhibitory effect on enzyme activities must be taken into account in intermethod comparisons, because in some methods, it may be removed in a pretreatment step.

摘要

我们研究了在-20℃储存12个月期间,通过凝胶过滤制备并补充了白蛋白、或乙二醇、或乙二醇加白蛋白的尿液中N-乙酰-β-D-葡萄糖苷酶(EC 3.2.1.30)、丙氨酸氨基肽酶(EC 3.4.11.2)、碱性磷酸酶(EC 3.1.3.1)、γ-谷氨酰转移酶(EC 2.3.2.2)和溶菌酶(EC 3.2.1.17)的稳定性。通过对每月值与时间进行线性回归分析来评估稳定性。如果将起始酶活性的最大变化10%视为可接受的,那么除γ-谷氨酰转移酶外,所有酶在所有三种对照材料中均可在约一年内保持稳定。如果使用乙二醇作为稳定剂,必须对其适用性进行测试,并且在方法间比较时必须考虑其对酶活性的抑制作用,因为在某些方法中,它可能会在预处理步骤中被去除。

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