Nishida Y, Ikematsu S, Fukutake K, Fujimaki M, Fukutake K, Kakishita E
Thromb Res. 1984 Oct 15;36(2):123-31. doi: 10.1016/0049-3848(84)90334-7.
A new sensitive, reproducible and simple assay for factor XIII activity was developed, in which fluorescent dansylcadaverine (DC) is incorporated into casein and DC-casein is separated from free DC by gel filtration. A good correlation was found between our method and Lorand's. The main advantages of our method are: (1) our assay technique is simple with good reproducibility and takes only a couple of hours; (2) the detectable limit of factor XIII activity is about 1% of normal pool plasma, but, if necessary, can be lowered by increasing the sample amount and lengthening the reaction time.
开发了一种新的用于检测因子 XIII 活性的灵敏、可重复且简单的检测方法,该方法中,荧光丹磺酰尸胺(DC)被掺入酪蛋白中,并且通过凝胶过滤将 DC-酪蛋白与游离 DC 分离。我们的方法与罗兰德的方法之间发现有良好的相关性。我们方法的主要优点是:(1)我们的检测技术简单,具有良好的可重复性,只需几个小时;(2)因子 XIII 活性的可检测限约为正常混合血浆的 1%,但如有必要,可通过增加样品量和延长反应时间来降低检测限。