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Procedure and diagnostics for the qualitative or quantitative detection of antibodies and for the determination of their Avidity

机译:用于抗体定性或定量检测以及抗体亲和力测定的程序和诊断方法

摘要

Method for quantitative or qualitative determination of an antibody (Ab) by reaction with its cognate antigen (Ag), selective destabilization of complexes formed with Ab of low affinity and measuring the degree of Ab-Ag binding. The new feature is that the protein denaturant (I) used is adjusted to a pH outside the normal range (5-9) for immunological assays. Independent claims are also included for: (1) method for determining the affinity of Ab; (2) method for differentiating early and late infections using the method of (1); (3) method for detecting acute or recent measles infection, first infection by cytomegalovirus, Epstein-Barr virus or herpes simplex virus, or Toxoplasma gondii infection; (4) wash or sample dilution buffers for immunoassays adjusted to pH outside the range 5-9; and (5) diagnostic composition for performing the new processes.
机译:通过与抗体的同源抗原(Ag)反应,对具有低亲和力的Ab形成的复合物进行选择性去稳定化并测量Ab-Ag结合程度的方法来定量或定性确定抗体(Ab)的方法。新功能是将用于免疫分析的蛋白质变性剂(I)的pH调节至正常范围(5-9)以外。还包括以下独立权利要求:(1)确定抗体亲和力的方法; (2)使用(1)的方法区分早期和晚期感染的方法; (3)用于检测急性或最近的麻疹感染,巨细胞病毒,爱泼斯坦-巴尔病毒或单纯疱疹病毒的首次感染或弓形虫感染的检测方法; (4)用于免疫测定的洗涤或样品稀释缓冲液,调节至pH值超出5-9的范围; (5)用于执行新过程的诊断成分。

著录项

  • 公开/公告号DE50302156D1

    专利类型

  • 公开/公告日2006-04-06

    原文格式PDF

  • 申请/专利权人 INSTITUT VIRION/SERION GMBH;

    申请/专利号DE20035002156T

  • 发明设计人 HERMANN DR.;

    申请日2003-05-30

  • 分类号G01N33/543;G01N33/53;

  • 国家 DE

  • 入库时间 2022-08-21 21:19:23

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