首页> 外国专利> HIGH SENSITIVE IMMUNOLOGICAL DETECTION MEASURING METHOD FOR MICROORGANISM (BACTERIA, FUNGUS, VIRUS, PRODUCING SUBSTANCE) AND QUANTITATIVE METHOD

HIGH SENSITIVE IMMUNOLOGICAL DETECTION MEASURING METHOD FOR MICROORGANISM (BACTERIA, FUNGUS, VIRUS, PRODUCING SUBSTANCE) AND QUANTITATIVE METHOD

机译:微生物(细菌,真菌,病毒,生产物质)的高灵敏免疫检测方法及定量方法

摘要

PROBLEM TO BE SOLVED: To quantitatively detect a microorganism at a high sensitivity by producing a product by adding dropwise an enzyme substrate to a microorganism dual antibody binding substance remained on a solid phase matrix. ;SOLUTION: A solid phase matrix requires a pore diameter through which a microorganism can not be passed. For example, the pore diameter is particularly preferably 0.22-0.45 μm in a bacteria inspection and 0.80 μm in the case of a fungus. After the microorganism is filtered and accumulated on the solid phase matrix if necessary, a sample solution remained on the solid phase matrix is washed with a washing liquid. A specific antibody to be detected is added dropwise to the microorganism on the solid phase matrix and a reaction of the microorganism with the antibody is carried out. As the antibody, an antibody against a specific microorganism is sometimes used if desired. A substance necessary for an enzymatic reaction is added dropwise to an enzyme labeled antibody binding microorganism captured and remained on the solid phase matrix and an enzymatic reaction is carried out. A product is finally produced and is measured. A determination of the desired microorganism is carried out by previously preparing a calibration line representing a reaction amount in the case of using a constant amount of antigen and applying it thereto.;COPYRIGHT: (C)2000,JPO
机译:解决的问题:通过将酶底物滴加到残留在固相基质上的微生物中的双重抗体结合物质来生产产物,从而以高灵敏度定量检测微生物。 ;解决方案:固相基质需要一个孔径,微生物无法通过该孔径。例如,在细菌检查中,孔径特别优选为0.22-0.45μm,在真菌的情况下为0.80μm。在必要时将微生物过滤并累积在固相基质上之后,用洗涤液洗涤残留在固相基质上的样品溶液。将待检测的特异性抗体滴加到固相基质上的微生物中,并使微生物与抗体反应。作为抗体,根据需要有时使用针对特定微生物的抗体。将酶促反应所需的物质滴加到捕获并保留在固相基质上的酶标记的抗体结合微生物中,并进行酶促反应。最终生产并测量产品。在使用恒定量的抗原的情况下,通过预先准备代表反应量的校准线并对其进行应用,来确定所需微生物。COPYRIGHT:(C)2000,JPO

著录项

  • 公开/公告号JP2000088854A

    专利类型

  • 公开/公告日2000-03-31

    原文格式PDF

  • 申请/专利权人 UMA:KK;

    申请/专利号JP19980295968

  • 发明设计人 KARIYAMA HIDEMICHI;

    申请日1998-09-11

  • 分类号G01N33/569;C12M1/34;G01N33/531;G01N33/535;G01N33/543;G01N33/577;

  • 国家 JP

  • 入库时间 2022-08-22 01:59:46

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