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Method for the quantitative determination of a serum protein in turbid serum and plasma samples, and reagent for using this method

机译:混浊的血清和血浆样品中血清蛋白的定量测定方法及使用该试剂的试剂

摘要

The invention relates to a method for the quantitative determination of a serum protein, in particular apolipoprotein in cloudy serum or plasma samples by turbidity measurement, in which the measurement is carried out after carrying out an immunological reaction with the corresponding antibody in the presence of a cationic surfactant of the general formula CH3- (CH2) mR- (CH2-CH2-O) nH in which R means IMAGE where Y is H- or CH3- (CH2) q-, m and q, identical or different, integers between 6 and 26, preferably between 6 and 18 , n is an integer between 7 and 50, preferably between 7 and 25 and x 7 or 8, the surfactant in a concentration of 10 - 3 to 10 -? Vol% is used. The measurement can also be carried out after enzymatic degradation of the lipids and subsequent immunological reaction with the corresponding antibody in the presence of a nonionic surfactant of the general formula mentioned in which R has the meanings given above or IMAGE where R 'is CH3 or C2H5, m a integer between 6 and 26, preferably between 6 and 18, n is an integer between 7 and 50, preferably between 7 and 25 and x is 7 or 8. The invention further relates to the use of a surfactant of the general formula mentioned for serum processing for the quantitative determination of an apolipoprotein and an agent for serum processing for the quantitative determination of an apolipoprotein, consisting of a mixture of at least one lipid degradation enzyme and a surfactant of the named general formula.
机译:本发明涉及一种通过浊度测定法定量测定浑浊的血清或血浆样品中的血清蛋白质,特别是载脂蛋白的方法,其中该测定是在存在相应抗原的情况下与相应抗体进行免疫反应后进行的。通式CH3-(CH2)mR-(CH2-CH2-O)nH的阳离子表面活性剂,其中R表示,其中Y是H-或CH3-(CH2)q-,m和q相同或不同,表面活性剂的浓度为10 -3至10 -3,n为6至26之间,优选6至18之间的整数,n为7至50之间的整数,优选7至25之间的整数和x 7或8。使用Vol%。还可以在脂质进行酶促降解并随后与相应的抗体发生免疫反应之后,在上述通式的非离子表面活性剂存在下进行测量,其中R具有上述含义或,其中R'为CH3或C 2 H 5,m为6至26之间,优选为6至18之间的整数,n为7至50之间的整数,优选为7至25之间,x为7或8。本发明进一步涉及一般表面活性剂的用途。用于定量处理载脂蛋白的血清处理剂和用于定量处理载脂蛋白的血清剂,由至少一种脂质降解酶和上述通式的表面活性剂的混合物组成。

著录项

  • 公开/公告号EP0008338A1

    专利类型

  • 公开/公告日1980-03-05

    原文格式PDF

  • 申请/专利权人 HEUCK CLAUS-CHRISTIAN DR. DR.;

    申请/专利号EP19790102204

  • 发明设计人 HEUCK CLAUS-CHRISTIAN DR. DR.;

    申请日1979-07-02

  • 分类号G01N33/68;G01N33/92;

  • 国家 EP

  • 入库时间 2022-08-22 17:57:51

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