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METHOD AND REAGENT FOR QUANTITATIVE DETERMINATION OF ANTI-STREPTOLYSIN O ANTIBODY

机译:抗体测定抗体中抗链球菌溶血素的方法和试剂

摘要

PURPOSE:To improve the accuracy of quantitative determination by mixing serum and the latex of an insoluble carrier which is sensitized with streptolysin O and has 0.2mum grain size in such a manner that the final concn. attains 0.05wt%, inducing a latex agglutination reaction by the antigen-antibody reaction and measuring light absorbency at 530-600nm wavelength. CONSTITUTION:The serum and the latex of the insoluble carrier which is sensitized with the streptolysin and has about 0.05-0.2mum grain size are mixed with a phosphoric acid buffer soln., etc. as a medium in such a manner that the final concn. of the insoluble carrier attains 0.05wt% to prepare a mixed liquid. The mixed liquid induces the latex agglutination reaction by the antigen- antibody reaction and the light absorbency of the reaction liquid after the reaction is measured by using the adequate wavelength of 530-600nm. The optical path length of the cell in the absorbency measurement is preferably about 5-10mm.
机译:目的:通过将血清和乳胶混合在一起,以提高定量测定的准确性,该不溶性载体被链球菌溶血素O致敏,且粒径小于0.2微米,以使最终浓度降低。达到<0.05wt%,通过抗原-抗体反应诱导乳胶凝集反应,并测量530-600nm波长下的吸光度。组成:用链球菌溶血素敏化并具有约0.05-0.2μm粒径的不溶性载体的血清和胶乳与磷酸缓冲液等作为介质混合,以使最终浓度得以降低。的不溶性载体的重量达到<0.05wt%以制备混合液体。混合液通过抗原抗体反应引起胶乳凝集反应,反应后的反应液的吸光度通过使用适当的530〜600nm的波长进行测定。吸光度测量中的电池的光路长度优选为约5-10mm。

著录项

  • 公开/公告号JPS61182578A

    专利类型

  • 公开/公告日1986-08-15

    原文格式PDF

  • 申请/专利权人 HITACHI CHEM CO LTD;

    申请/专利号JP19850024223

  • 发明设计人 IIJIMA HIROMI;TANNO KAZUNOBU;

    申请日1985-02-08

  • 分类号G01N33/569;G01N33/543;

  • 国家 JP

  • 入库时间 2022-08-22 07:49:43

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