Process for photometric determination of protein C and/or protein S
    2.
    发明授权
    Process for photometric determination of protein C and/or protein S 失效
    蛋白C和/或蛋白S的光度测定方法

    公开(公告)号:US5001069A

    公开(公告)日:1991-03-19

    申请号:US256100

    申请日:1988-10-04

    摘要: The present invention provides a process for the photometric determination of protein C and/or protein S activity, especially in plasma, wherein the sample containing the protein C and/or protein S to be determined is incubated with a protein C activator from snake venom with the formation of activated protein C and/or protein S and the decrease of the formation of thrombin from prothrombin brought about by the coagulation factors and the activators thereof is determined by means of a chromogenic thrombin substrate.

    摘要翻译: 本发明提供了一种用于光度测定蛋白C和/或蛋白S活性的方法,特别是在血浆中,其中将待测定的含有蛋白C和/或蛋白S的样品与来自蛇毒的蛋白C激活剂一起温育, 活化蛋白C和/或蛋白S的形成以及由凝血因子及其活化剂引起的凝血酶原形成的凝血酶的形成减少是通过显色凝血酶底物来确定的。

    Analysis element for determination of a coagulation parameter
    6.
    发明授权
    Analysis element for determination of a coagulation parameter 失效
    用于测定凝血参数的分析元素

    公开(公告)号:US4861712A

    公开(公告)日:1989-08-29

    申请号:US046659

    申请日:1987-05-04

    摘要: The present invention provides an analysis element for the determination of coagulation parameters with the help of a detectable or a detection reaction-initiating substrate of a protease of the blood coagulation system and at least one factor and/or co-factor of the blood coagulation system and a buffer substance, wherein the factor and/or co-factor, together with a water-soluble, non-ionic polymer which does not falsely influence the course of the coagulation cascade, is impregnated on an open, planar composite structure which consists of a material which does not have a disturbing influence on the course of the coagulation.

    摘要翻译: 本发明提供了一种用于通过凝血系统的蛋白酶的可检测或检测反应引发底物和血液凝固系统的至少一个因子和/或辅因子来确定凝血参数的分析元件 和缓冲物质,其中所述因子和/或辅助因子与不会对凝血级联进程没有错误影响的水溶性非离子聚合物一起浸渍在开放的平面复合结构上,所述平面复合结构由 不会对凝固过程产生干扰的材料。

    Process for determining the perkallikrein content and the partial
thromboplastin time of a plasma sample
    7.
    发明授权
    Process for determining the perkallikrein content and the partial thromboplastin time of a plasma sample 失效
    用于测定血浆样品的促凝血素蛋白含量和部分凝血活酶时间的方法

    公开(公告)号:US4732860A

    公开(公告)日:1988-03-22

    申请号:US822364

    申请日:1986-01-24

    IPC分类号: G01N33/86 C12Q1/56 G01N21/78

    摘要: The present invention provides a process for the photometric determination of prekallikrein in plasma, wherein plasma is incubated with a surface activator, the extinction obtained is measured, a chromogenic thrombin substrate is then added thereto, the optically determinable group liberated therefrom is measured at short time intervals or continuously and the gradient of the linear part of the curve obtained by plotting the time against the extinction is determined as a measure of the prekallikrein content. The partial thromboplastin time of plasma is simultaneously determined by carrying out the incubation in the presence of calcium ions and a phospholipid and measuring the time it takes the extinction to reach a predetermined level.

    摘要翻译: 本发明提供了一种用于光度测定血浆中前激肽释放酶的方法,其中将血浆与表面活化剂一起温育,测量所得的消光,然后向其中加入显色凝血酶底物,在短时间内测定从其释放的光学上可测定的基团 间隔或连续,并且通过绘制针对灭绝的时间获得的曲线的线性部分的梯度被确定为前激肽释放素含量的量度。 通过在钙离子和磷脂的存在下进行孵育并测量灭绝达到预定水平的时间,同时测定血浆的部分凝血活酶时间。

    Process and reagent for the determination of fibrin monomer in plasma
    8.
    发明授权
    Process and reagent for the determination of fibrin monomer in plasma 失效
    用于测定血浆中纤维蛋白单体的方法和试剂

    公开(公告)号:US4710459A

    公开(公告)日:1987-12-01

    申请号:US767865

    申请日:1985-08-21

    摘要: The present invention provides a process for the determination of fibrin monomer in plasma, wherein a plasma sample containing fibrin monomer and freed from plasmin inhibitors is incubated in buffered solution with tissue plasminogen activator (EPA), plasminogen and a chromogenic plasmin substrate and the color formed is measured as a measure of the amount of fibrin monomer.The present invention also provides a reagent for the determination of fibrin monomer in plasma, wherein it contains plasminogen, tissue plasminogen activator (EPA), chromogenic plasmin substrate and buffer (pH 7.0 to 9.0).

    摘要翻译: 本发明提供了一种测定血浆中纤维蛋白单体的方法,其中将含有纤维蛋白单体的血浆样品与纤维蛋白溶酶抑制剂无关的蛋白质在缓冲液中与组织纤溶酶原激活剂(EPA),纤溶酶原和色素性纤维蛋白溶酶基质孵育,并形成颜色 被测量为纤维蛋白单体量的量度。 本发明还提供了用于测定血浆中纤维蛋白单体的试剂,其中它含有纤溶酶原,组织纤溶酶原激活剂(EPA),显色性纤溶酶底物和缓冲液(pH 7.0-9.0)。

    Process for specific determination of cholesterol in the presence of the
HDL fraction in serum
    9.
    发明授权
    Process for specific determination of cholesterol in the presence of the HDL fraction in serum 失效
    在血清中HDL级分存在下特异性测定胆固醇的方法

    公开(公告)号:US4544630A

    公开(公告)日:1985-10-01

    申请号:US468792

    申请日:1983-02-22

    CPC分类号: C12Q1/60

    摘要: The present invention provides a process for the specific determination of the cholesterol of the LDL fraction in the presence of the HDL fraction of the lipoproteins of serum by the action of cholesterol esterase for the liberation of the cholesterol and oxidation of the liberated cholesterol with cholesterol oxidase and oxygen with the formation of hydrogen peroxide and cholestenone and kinetic measurement of the change of one of the reaction components of the oxidase reaction, especially the formation of hydrogen peroxide, wherein the measurement is carried out in a predetermined period of time, the reaction solution having a tenside concentration of 0.01 to 1.5 mmol/liter, a cholesterol esterase concentration of 0.1 to 30 U/ml. and a pH value of 6.5 to 8.0.The present invention also provides a reagent for carrying out this process.

    摘要翻译: 本发明提供了一种在胆固醇酯酶的作用下,通过胆固醇释放和胆固醇氧化酶氧化释放的胆固醇,在血清脂蛋白的HDL部分存在下,特异性测定LDL级分的胆固醇的方法 和氧气,形成过氧化氢和胆甾烯酮,动力学测量氧化酶反应的一种反应成分的变化,特别是过氧化氢的形成,其中测量在预定时间内进行,反应溶液 其表面活性剂浓度为0.01〜1.5mmol / l,胆固醇酯酶浓度为0.1〜30U / ml。 pH值为6.5〜8.0。 本发明还提供了一种用于进行该方法的试剂。