首页> 外国专利> TEST immunoassay for the semiquantitative determination of allergen-specific IgE and IgG-antibodies for the diagnosis of mycosis (IFTS-MICS-IgE-IgG-AT)

TEST immunoassay for the semiquantitative determination of allergen-specific IgE and IgG-antibodies for the diagnosis of mycosis (IFTS-MICS-IgE-IgG-AT)

机译:TEST免疫测定法,用于半定量测定过敏原特异性IgE和IgG抗体,用于诊断真菌病(IFTS-MICS-IgE-IgG-AT)

摘要

Test - immunoassay for the semiquantitative determination of allergen specific IgE and IgG - antibodies for diagnosis of fungal infections (IFTS-myco-IgE-IgG-AT) The utility model is used in the medical diagnostic laboratory. The task performed by the proposed test -system IFTS-myco-IgE-IgG-AT, developed by solid phase sandwich method in a 96-well plate stripirovannom using monoclonal antibodies comprising the peroxidase conjugates, of anti-mAb-IgE and MKAT- anti-IgG. The method is based on a combination of immunological reactions in the first stage between fungal allergens immobilized on a polystyrene microtiter plate, and specific to these allergens IgE - and IgG - the antibodies from the serum sample to form a solid phase immunological complexes AG 1-AT. In the second stage between complexes of AH-1 and AT-conjugates MAbs and anti-IgE mAb-anti-IgG to form an immunological complex AT-AT 1 -AT 2, labeled peroxidase enzyme. Subsequent enzymatic color reaction occurs between the peroxidase and the substrate. cleavage reaction products are converted chromogen molecules - TMB into a colored derivative whose amount is proportional to enzyme activity. The degree of staining is considered photometrically at 450 nm. Contents of allergen-IgE-IgG-antibodies in the samples is expressed in grades (1-4) corresponding to low, medium, high and moderately high concentrations of IgE and IgG. The utility model is a kit, which includes a kit comprising polystyrene plates with immobilized allergens reference - serum wash solution chromogen substrate, Stop - reagent and instructions for use that are packaged in one box.
机译:用于半定量测定过敏原特异性IgE和IgG的试验-免疫测定-用于诊断真菌感染的抗体(IFTS-myco-IgE-IgG-AT)本实用新型在医学诊断实验室中使用。由拟议的测试系统IFTS-myco-IgE-IgG-AT执行的任务,该系统通过固相夹心法在96孔板Stripirovannom中使用抗mAb-IgE和MKAT-anti的包含过氧化物酶偶联物的单克隆抗体开发-IgG。该方法基于固定在聚苯乙烯微量滴定板上的真菌变应原与特异性针对这些变应原IgE-和IgG-血清样品中抗体形成固相免疫复合物AG的免疫反应的第一阶段的组合。 > 1-AT。 AH-1 和AT结合物MAb与抗IgE mAb-抗IgG的复合物之间形成第二步,形成免疫复合物AT-AT 1 -AT 2 标记的过氧化物酶。随后的酶显色反应在过氧化物酶和底物之间发生。裂解反应产物被转化成色原分子-TMB成为有色衍生物,其数量与酶活性成正比。在450nm处以光度法考虑染色的程度。样品中过敏原-IgE-IgG-抗体的含量以等级(1-4)表示,分别对应于低,中,高和中等高浓度的IgE和IgG。本实用新型是一种试剂盒,其包括一个试剂盒,该试剂盒包括固定有变应原参考的聚苯乙烯板-血清洗涤液色原底物,Stop-试剂和使用说明书,它们包装在一个盒子中。

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