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use of crotalus viridis helleri venom for the determination of activated protein c activity

机译:响尾蛇蛇毒用于测定活化蛋白c活性的用途

摘要

A process for determining a resistance to activated protein C of a test specimen of human plasma following the steps of: (1) mixing together (a) the test specimen of human plasma, (b) a reactant deficient in factor V which supplies at least most of the coagulation factors other than factor V, and (c) the venom of Crotalus viridis helleri which specifically activates factor X to Xa, and incubating the mixture of (a), (b) and (c) for at least one minute at a temperature of between 10 and 45° C.; (2) introducing into the incubated mixture(i) Ca2+ or (ii) Ca2++exogenic activated protein C; and (3) determining the coagulation time (i) in the absence of activated protein C and (ii) in the presence of activated protein C. Steps (1) to (3) are repeated, but replacing, in step (1), the test specimen with a normal plasma as control and correlating resistance to activated protein C by comparing the determinations made in steps for the test specimen and for the normal plasma. The initiation of coagulation is caused by activating factor X to Xa using the venom of Crotalus viridis helleri in the presence of (i) Ca2+ or (ii) Ca2++ exogenic activated protein C.
机译:确定人类血浆试样对活化蛋白C的抗性的方法,其步骤如下:(1)混合(a)人类血浆试样,(b)因子V缺乏的反应物,其至少提供除凝血因子V以外的大多数凝血因子,以及(c)特效激活X因子至Xa的猪屎豆的毒液,并将(a),(b)和(c)的混合物在200℃温育至少一分钟。温度在10至45℃之间; (2)引入温育混合物(i)Ca2 +或(ii)Ca2 ++外源性活化蛋白C;和(3)确定凝固时间(i)在没有活化蛋白C的情况下和(ii)在活化蛋白C的情况下。重复步骤(1)至(3),但在步骤(1)中代替,通过比较在测试样品和正常血浆中分步进行的测定,以正常血浆为对照的测试样品,并将其与活化蛋白C的抗性相关。在(i)Ca2 +或(ii)Ca2 ++外源性活化蛋白C的存在下,利用猪屎豆的毒液将因子X活化为Xa引起凝血的开始。

著录项

  • 公开/公告号DE69801806D1

    专利类型

  • 公开/公告日2001-10-31

    原文格式PDF

  • 申请/专利权人 SOCIETE DIAGNOSTICA-STAGO ASNIERES;

    申请/专利号DE1998601806T

  • 发明设计人 VAN DREDEN PATRICK;

    申请日1998-06-05

  • 分类号G01N33/86;

  • 国家 DE

  • 入库时间 2022-08-22 01:08:08

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