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一种用于纤溶酶原激活剂的灵敏且特异的检测方法。

A sensitive and specific assay for plasminogen activators.

作者信息

Smith D S, Harmon J, Owen W G

出版信息

Thromb Res. 1985 Feb 15;37(4):533-41. doi: 10.1016/0049-3848(85)90099-4.

Abstract

A simple, sensitive and specific assay for plasminogen activators is described. The assay utilizes fluorescein-labeled fibrinogen or fibrin at low concentrations, and enables simultaneous evaluation of the plasminogen and fibrin dependence of the reaction, that is, discrimination of tissue-type and urokinase-type plasminogen activators, and non-specific proteolysis. Addition of antisera verify identification of the activator species. The assay reagent contains plasminogen and fluorescein-labeled fibrinogen, to which is added the specimen and then then thrombin, either at the initiation or the termination of the reaction. Supernatant fluorescence is proportional to plasminogen activator concentration. With a four-hour incubation, 1 milliunit (14 pg) of tissue (melanoma) plasminogen activator (TPA) or 2 milliunit (36 pg) of urokinase (UK) may be detected.

摘要

本文描述了一种简单、灵敏且特异的纤溶酶原激活剂检测方法。该检测方法使用低浓度的荧光素标记纤维蛋白原或纤维蛋白,能够同时评估反应对纤溶酶原和纤维蛋白的依赖性,即区分组织型和尿激酶型纤溶酶原激活剂以及非特异性蛋白水解。加入抗血清可验证激活剂种类的鉴定。检测试剂含有纤溶酶原和荧光素标记纤维蛋白原,在反应开始或结束时加入标本,然后加入凝血酶。上清液荧光与纤溶酶原激活剂浓度成正比。经过4小时孵育,可检测到1毫单位(14皮克)的组织(黑色素瘤)纤溶酶原激活剂(TPA)或2毫单位(36皮克)的尿激酶(UK)。

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