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    • 74. 发明授权
    • Method for measuring antigens or antibodies in biological fluids using
ligand labeled antigens or ligand labeled antibodies
    • 使用配体标记的抗原或配体标记的抗体测量生物流体中的抗原或抗体的方法
    • US4778751A
    • 1988-10-18
    • US862123
    • 1986-05-12
    • A. Said El ShamiOlusola O. AlabaCharles A. Kasal
    • A. Said El ShamiOlusola O. AlabaCharles A. Kasal
    • G01N33/545G01N33/531G01N33/538G01N33/543G01N33/548G01N33/537
    • G01N33/54306G01N33/531G01N33/538G01N33/548Y10S435/805Y10S435/971Y10S436/823
    • The method of measuring circulating antigens or antibodies by using a ligand labeled specific antigen or ligand labeled specific antibody chemically attached to a soluble matrix or backbone, a differently labeled anti-antigen or anti-antibody and a solid phase anti-ligand directed at the ligand attached to the specific antigen or specific antibody. This is achieved by either one or two analytical schemes:(a) Reacting a patient sample with a ligand labeled specific antigen or a ligand labeled specific antibody in the liquid phase in the presence of a differently labeled specific anti-antigen or labeled specific anti-antibody. This immunological complex is reacted with an immobilized anti-ligand on a solid support which is directed against the ligand attached to the specific antigen or antibody through the liquid matrix. Subsequently the solid phase is washed and checked for the label on the anti-antigen or anti-antibody which is directly proportional to the concentration of specific antigen or antibody.(b) Reacting a patient sample with the ligand labeled specific antigen or a ligand labeled specific antibody in the liquid phase, then contacting said liquid phase with an immobilized anti-ligand on a solid support; washing the solid support and reacting it with a differently labeled anti-antigen or anti-antibody. This is followed by re-washing of the solid support and checking for the presence of the label attached to the anti-antigen or anti-antibody which is directly proportional to the concentration of the specific antigen or antibody. The ligand is covalently attached to the specific antigen or antibody through a soluble liquid matrix or backbone to which the specific antigen or antibody has been chemically attached. This invention is applicable to a wide variety of antigen or antibody detection as described herein.
    • 通过使用化学连接到可溶性基质或骨架的配体标记的特异性抗原或配体标记的特异性抗体,不同标记的抗原或抗体抗体和指向配体的固相抗配体来测量循环抗原或抗体的方法 附着于特异性抗原或特异性抗体。 这通过以下一种或两种分析方案实现:(a)在不同标记的特异性抗原或标记的特异性抗原的存在下,在液相中用配体标记的特异性抗原或配体标记的特异性抗体反应患者样品, 抗体。 该免疫复合物与固定支持物上的固定化抗配体反应,所述固定支持物通过液体基质针对与特定抗原或抗体连接的配体。 随后洗涤固相并检查抗原或抗体上的标记,其与特异性抗原或抗体的浓度成正比。 (b)在液相中用配体标记的特异抗原或配体标记的特异性抗体反应患者样品,然后将所述液相与固定支持物上的固定化抗配体接触; 洗涤固体支持物并使其与不同标记的抗原或抗体抗体反应。 然后重新洗涤固体支持物并检查与抗原或抗体的附着物的存在,其与特异性抗原或抗体的浓度成正比。 配体通过特定抗原或抗体化学连接的可溶性液体基质或骨架共价连接到特异性抗原或抗体上。 本发明可应用于本文所述的多种抗原或抗体检测。
    • 75. 发明授权
    • Assay kit and method for the determination of antibody class and subclass
    • 用于测定抗体类和亚类的测定试剂盒和方法
    • US4727037A
    • 1988-02-23
    • US580519
    • 1984-02-15
    • David B. Ring
    • David B. Ring
    • G01N33/543G01N33/548G01N33/68G01N33/53G01N33/577
    • G01N33/548G01N33/543G01N33/6854Y10S435/805Y10S435/81Y10S435/97Y10S436/808Y10S436/809Y10S436/81
    • A method of rapid determination of the isotype class for a panel of monoclonal antibodies is described. The assay comprises adsorbing on a solid support medium antibodies directed to specific immunoglobulin heavy and light chains. Once such isotype-specific antibodies are bound to the nitrocellulose paper, the treated strips can be incubated with the monoclonal antibody of interest. Upon formation of a complex between the specific iso-type antisera and the monoclonal antibody, the complex is visualized by reaction with a chromogenic substance. In the preferred embodiment of the invention, the treated nitrocellulose strips are stored in kit form. Using these prepared strips, the isotyping assay can be performed in less than two hours with a minimum of technical manipulation and expenditure of reagents.
    • 描述了一组快速测定单克隆抗体单克隆抗体类别的方法。 该测定包括吸附在固体支持培养基上针对特异性免疫球蛋白重链和轻链的抗体。 一旦这样的同种型特异性抗体与硝化纤维素纸结合,则处理的条可以与感兴趣的单克隆抗体一起温育。 在形成特异性异型抗血清和单克隆抗体之间的复合物时,通过与显色物质的反应可视化复合物。 在本发明的优选实施方案中,经处理的硝酸纤维素条以试剂盒形式储存。 使用这些制备的条带,可以在不到两个小时内进行同型化分析,同时以最小的技术操作和试剂消耗。
    • 76. 发明授权
    • Multiple-component binding assay system and method of making and using it
    • 多组分结合测定系统及其制备和使用方法
    • US4459360A
    • 1984-07-10
    • US308935
    • 1981-10-05
    • Vincent A. Marinkovich
    • Vincent A. Marinkovich
    • C12M1/34A61K39/36B65D71/00C12Q1/00G01N33/52G01N33/53G01N33/543G01N33/548G01N33/58G01N33/60G01N23/06
    • G01N33/521G01N33/548Y10S436/804Y10S436/808Y10S436/81
    • A multiple component binding assay system, and related methods of making and using it, having a plurality of coated filaments mounted at their opposite ends on a support, in a predetermined spaced relationship, for simultaneously screening a liquid test sample for a plurality of components. The system is particularly suitable for screening the sample for IgE class antibodies specific for certain allergens. The filaments are preferably cotton threads, each thread binding a different allergen through a covalent bond. The support, which is preferably cut away adjacent the mid-portion of each filament to reduce background interference, is composed of a plastic or other water insoluble material, permitting inexpensive and relatively simple manufacture. After any IgE class antibodies present in the liquid sample have reacted with the corresponding allergens coated on the filaments, they are detected using second antibodies labeled with radioactive, fluorescent or enzymatic tracers. By using a high energy radioactive tracer, such as .sup.125 I, autoradiographic techniques with phosphor screen enhancement allow for diagnostic analysis by a densitometer or even the unaided human eye.
    • 多组分结合测定系统及其制备和使用它的相关方法,其具有以预定的间隔关系安装在支撑体上的相对端的多个涂层细丝,用于同时筛选多个组分的液体测试样品。 该系统特别适用于筛选样品中特定于某些过敏原的IgE类抗体。 长丝优选为棉线,每根线通过共价键结合不同的变应原。 优选地,邻近每根丝的中间部分切割以减少背景干扰的支撑体由塑料或其它水不溶性材料组成,允许廉价且相对简单的制造。 在液体样品中存在的任何IgE类抗体已经与涂覆在细丝上的相应变应原反应后,使用用放射性,荧光或酶示踪剂标记的第二抗体检测它们。 通过使用诸如125I的高能放射性示踪剂,具有荧光屏增强的放射自显影技术允许通过密度计或甚至无人检测的眼睛进行诊断分析。