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用于尿激酶的灵敏放射化学酯酶测定法。

Sensitive radiochemical esterolytic assays for urokinase.

作者信息

Imanari T, Wilcox G M, Pisano J J

出版信息

Clin Chim Acta. 1976 Sep 6;71(2):267-76. doi: 10.1016/0009-8981(76)90540-4.

Abstract

Two radiochemical esterolytic assays for urokinase are described. One assay is based on the urokinase-dependent hydrolysis of Nalpha-acetyl-glycyl-L-lysine [3H]methyl ester and the other on the urokinase-dependent activation of plasminogen and assay of generated plasmin with Nalpha-tosyl-L-arginine [3H]methyl ester. The assays are performed in tubes placed in liquid scintillation counting vials. At the end of the experiment generated [3H]methanol is extracted into the liquid scintillation cocktail and counted. Unhydrolyzed substrate largely remains in the aqueous phase and contributes only a small fraction of the counts. This facile separation of 3H-labeled alcohol from the ester substrate allows the simple and highly sensitive assay for urokinase. The assays give results in good agreement with the classical fibrin plate assay.

摘要

本文描述了两种用于检测尿激酶的放射化学酯解测定法。一种测定法基于尿激酶依赖的Nα-乙酰基-甘氨酰-L-赖氨酸[³H]甲酯的水解,另一种基于尿激酶依赖的纤溶酶原激活以及用Nα-甲苯磺酰-L-精氨酸[³H]甲酯检测生成的纤溶酶。测定在置于液体闪烁计数瓶中的试管中进行。实验结束时,生成的[³H]甲醇被萃取到液体闪烁鸡尾酒中并进行计数。未水解的底物大部分保留在水相中,仅占计数的一小部分。这种将³H标记的醇与酯底物轻松分离的方法使得尿激酶的检测简单且高度灵敏。这些测定法的结果与经典的纤维蛋白平板测定法高度一致。

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