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Fetal fibronectin pregnancy test

机译:胎儿纤连蛋白妊娠试验

摘要

A method for determining normal intrauterine pregnancy during the first 20 weeks of pregnancy comprises obtaining a test sample; and determining the presence of a fetal restricted antigen in the sample. The test sample is removed the vaginal cavity in the vicinity of the cervical canal and/or the cervical os. One fetal restricted antigen is fetal fibronectin.PPIn one embodiment of this invention, the test sample is contacted with an insoluble support to which anti-(fetal restricted antigen) antibody is adhered, and the fetal restricted antigen binding to the support is determined. Alternatively, the test sample is contacted with an insoluble support to which is adhered an antibody which binds a class of substances including the fetal restricted antigen; and the fetal restricted antigen binding to the support is determined. Reagents and reagent kits are also included.
机译:一种用于在怀孕的前20周内确定正常的子宫内妊娠的方法,包括获得测试样品;以及确定样品中是否存在胎儿限制性抗原。将测试样品从子宫颈管和/或子宫颈口附近的阴道腔中取出。一种胎儿限制性抗原是胎儿纤连蛋白。在本发明的一个实施方案中,使测试样品与不溶性支持物接触,抗-(胎儿限制性抗原)抗体附着在该不溶性支持物上,并且胎儿限制性抗原与确定支持。或者,使测试样品与不溶性支持物接触,该不溶性支持物上附着有结合了包括胎儿限制性抗原在内的一类物质的抗体。并且确定胎儿限制性抗原与支持物的结合。还包括试剂和试剂盒。

著录项

  • 公开/公告号US5185270A

    专利类型

  • 公开/公告日1993-02-09

    原文格式PDF

  • 申请/专利权人 ADEZA BIOMEDICAL CORPORATION;

    申请/专利号US19880282426

  • 发明设计人 ANDREW E. SENYEI;NELSON N. H. TENG;

    申请日1988-12-12

  • 分类号G01N33/53;G01N33/48;

  • 国家 US

  • 入库时间 2022-08-22 04:58:49

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