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使用人工凝血试剂和改良显色测定法检测弗勒彻因子(血浆前激肽释放酶)。

Assay of Fletcher factor (plasma prekallikrein) using an artificial clotting reagent and a modified chromogenic assay.

作者信息

Soulier J P, Gozin D

出版信息

Thromb Haemost. 1979 Aug 31;42(2):538-47.

PMID:505362
Abstract

An artificial clotting reagent lacking in Fletcher factor (plasma prekallikrein, PPK) was made by mixing human plasma, activated by 5 mg/ml of celite, then kept 16 hours at 37 degrees to destroy most of the plasma kallikrein, plus rabbit plasma (which is devoid of XII and Fletcher activity). Chromogenic assay using a tripeptide substrate was also modified to exclude the interference of the endogenous contact factors. Celite eluate was used instead of kaolin or dextran sulphate for the activation. Using both these methods, it is possible to distinguish between Fletcher trait (PPK deficiency) and other contact factors such as factor XII and HMWK deficiencies, which do not activate with kaolin or dextran sulphate. These simple clotting and enzymatic assays give specific and well correlated results for PPK estimation.

摘要

一种缺乏弗勒彻因子(血浆前激肽释放酶,PPK)的人工凝血试剂,是通过将5毫克/毫升的硅藻土激活的人血浆混合制成,然后在37℃下保存16小时以破坏大部分血浆激肽释放酶,再加上兔血浆(兔血浆缺乏XII因子和弗勒彻活性)制成。使用三肽底物的发色测定法也进行了改进,以排除内源性接触因子的干扰。用硅藻土洗脱液代替高岭土或硫酸葡聚糖进行激活。使用这两种方法,可以区分弗勒彻特征(PPK缺乏)与其他接触因子,如XII因子和高分子量激肽原(HMWK)缺乏,后两者不能被高岭土或硫酸葡聚糖激活。这些简单的凝血和酶促测定法为PPK估计提供了特异且相关性良好的结果。

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