Method and substance for the enhanced labelling of cellular material
    81.
    发明授权
    Method and substance for the enhanced labelling of cellular material 失效
    增强细胞材料标记的方法和物质

    公开(公告)号:US4684609A

    公开(公告)日:1987-08-04

    申请号:US273813

    申请日:1981-06-15

    申请人: Su-Ming Hsu

    发明人: Su-Ming Hsu

    IPC分类号: G01N33/58 G01N33/54 C12N9/96

    摘要: An enhanced labelling complex for localizing markers on a prepared tissue section is disclosed. The complex includes both avidin components and biotinylated macromolecular components at a ratio preselected to provide a complex which is sufficiently large to include a large number of labels, and sufficiently small to penetrate the tissue section. The markers are localized by first introducing a biotinylated link into the tissue section and thereafter exposing the section to the labelling complex.

    摘要翻译: 公开了用于在制备的组织切片上定位标记物的增强的标记复合物。 复合物包括抗生物素蛋白组分和生物素化大分子组分,其预选比例提供了足够大的复合物,其包含大量标记,足够小以渗透组织切片。 通过首先将生物素化链接引入组织切片中,然后将该部分暴露于标记复合物来定位标记物。

    Target specific cross-linked heteroantibodies
    82.
    发明授权
    Target specific cross-linked heteroantibodies 失效
    靶标特异性交联异抗体

    公开(公告)号:US4676980A

    公开(公告)日:1987-06-30

    申请号:US778670

    申请日:1985-09-23

    摘要: The present invention discloses a target specific cross-linked heteroantibody and a method of producing the same. The cross-linked heteroantibodies of the present invention can cause normal autologous cells of the immune system to destroy any unwanted cell for which an antibody is available. Treatment or control of tumors, viral infected cells, fungi, bacteria, parasites and the like is now made possible through the use of the heteroantibody complex of the present invention.

    摘要翻译: 本发明公开了一种靶特异性交联异质体及其制造方法。 本发明的交联异抗体可引起免疫系统的正常自体细胞破坏抗体可用的任何不需要的细胞。 现在可以通过使用本发明的异抗体复合物来治疗或控制肿瘤,病毒感染的细胞,真菌,细菌,寄生虫等。

    Monoclonal antibody to Candida albicans cytoplasmic antigens and methods
of preparing same
    83.
    发明授权
    Monoclonal antibody to Candida albicans cytoplasmic antigens and methods of preparing same 失效
    白念珠菌细胞质抗原的单克隆抗体及其制备方法

    公开(公告)号:US4670382A

    公开(公告)日:1987-06-02

    申请号:US571129

    申请日:1984-01-16

    摘要: Two novel hybridoma cell lines, ATCC #HB-8397 and ATCC #HB-8398 produce monoclonal antibody monospecific to a single determinant shared by a set of three closely related cytoplasmic antigens of Candida albicans. The antigens have molecular weights of 120-135 Kd, 48-52 Kd, and 35-38 Kd. The hybridomas are formed by fusing splenocytes from immunized BALB/c mice with SP2/O-Ag 14 myeloma cells. Monoclonal and monospecific, polyclonal antibodies to these cytoplasmic antigens find application in the immunodiagnosis of Candida infections.A procedure is provided for preparing partially purified cytoplasmic antigen of pathogenic Candida species for administration to splenocyte-donating mice. Also provided is a method for the biochemical purification of cytoplasmic antigen of a pathogenic Candida species used for the preparation of monoclonal and monospecific, polyclonal antisera thereto.

    摘要翻译: 两种新型杂交瘤细胞系ATCC#HB-8397和ATCC#HB-8398产生单一抗体单特异性单个决定簇,由一组三个密切相关的白色念珠菌细胞质抗原共享。 抗原的分子量为120-135Kd,48-52Kd,和35-38Kd。 通过将免疫的BALB / c小鼠的脾细胞与SP2 / O-Ag14骨髓瘤细胞融合来形成杂交瘤。 针对这些细胞质抗原的单克隆和单特异性多克隆抗体可应用于念珠菌感染的免疫诊断。 提供了用于制备用于给予脾细胞供体小鼠的部分纯化的致病念珠菌种类的细胞质抗原的方法。 还提供了用于制备用于制备单克隆和单特异性多克隆抗血清的致病念珠菌物质的细胞质抗原的生物化学纯化的方法。

    Substrate for fluoroimmunoassay of biological fluids
    84.
    发明授权
    Substrate for fluoroimmunoassay of biological fluids 失效
    生物液体荧光免疫测定基质

    公开(公告)号:US4540660A

    公开(公告)日:1985-09-10

    申请号:US483055

    申请日:1983-04-07

    摘要: A substrate for fluoroimmunoassay is disclosed comprising a swellable, rehydratable polymeric protein-binding material forming a three-dimensional matrix; first particulate, light scattering centers distributed in the polymeric matrix capable of scattering visible light; and second particulate, light-scattering centers distributed in the polymeric matrix capable of reflecting fluorescent excitation light and absorbing all other light. The substrate efficiently binds proteins and enhances transmitted fluorescent light and thus increases the sensitivity of assays involving fluorescent measurements. The polymeric protein binding material is preferable an acrylic copolymer. The first light scattering centers are preferably oxides of titanium and zinc, and the second light-scattering centers are preferably a phthalocyanin compound.

    摘要翻译: 公开了用于荧光免疫测定的底物,其包含形成三维基质的可溶胀,可再水合的聚合蛋白结合材料; 分散在能够散射可见光的聚合物基质中的第一颗粒,光散射中心; 以及分布在能够反射荧光激发光并吸收所有其它光的聚合物基质中的第二颗粒状光散射中心。 底物有效地结合蛋白质并增强透射的荧光,从而增加涉及荧光测量的测定的灵敏度。 聚合蛋白结合材料优选为丙烯酸共聚物。 第一光散射中心优选为钛和锌的氧化物,第二光散射中心优选为酞菁化合物。

    Simultaneous calibration heterogeneous immunoassay
    85.
    发明授权
    Simultaneous calibration heterogeneous immunoassay 失效
    同时校准异种免疫测定

    公开(公告)号:US4540659A

    公开(公告)日:1985-09-10

    申请号:US399107

    申请日:1982-07-16

    IPC分类号: G01N33/542 G01N33/54 C12N9/96

    摘要: An assay method and compositions are provided for determining the presence of an analyte in a sample. The analyte is a member of an immunological pair (mip) comprising ligand and receptor. By providing a first measurement surface capable of specifically binding a labelled reagent in an amount depending upon the presence of analyte in the sample and a second calibration surface capable of binding a second labeled reagent in a manner unaffected by the presence of analyte in the sample, calibration of individual tests can be accomplished simultaneously with the performance of the test itself. A signal producing system includes an enzyme, a catalyst usually bonded to a mip which defines the first labeled reagent for binding to the measurement surface and the same catalyst conjugated to a ligand capable of binding to the calibration surface. Preferably, both labeled reagents have the same composition and the calibration surface includes anti-(first catalyst).

    摘要翻译: 提供测定方法和组合物以确定样品中分析物的存在。 分析物是包含配体和受体的免疫对(mip)的成员。 通过提供能够以取决于样品中分析物的存在的量特异性结合标记试剂的第一测量表面和能够以不受样品中分析物的存在影响的方式结合第二标记试剂的第二校准表面, 单独测试的校准可以与测试本身的性能同时完成。 信号产生系统包括酶,通常结合到mip上的催化剂,其定义用于结合测量表面的第一标记试剂和与能够结合校准表面的配体缀合的相同催化剂。 优选地,两个标记的试剂具有相同的组成,并且校准表面包括抗(第一催化剂)。

    Titration of group C streptococcal antibody
    87.
    发明授权
    Titration of group C streptococcal antibody 失效
    C组链球菌抗体滴定

    公开(公告)号:US4529582A

    公开(公告)日:1985-07-16

    申请号:US454908

    申请日:1982-12-30

    CPC分类号: A61K49/00 G01N33/56944

    摘要: Group C streptococcal antibody levels in a serum sample can be determined via passive protection test in susceptible animals. Test is based on property of protective antibody in the serum sample to reduce the virulence of a group C streptococcal challenge and provides a means for detecting whether an animal (e.g. horse) is susceptible to infection by group C streptococcal organism.

    摘要翻译: 血清样品中C组链球菌抗体水平可以通过易感动物的被动保护试验来测定。 测试基于血清样品中保护性抗体的性质,以降低C组链球菌攻击的毒力,并提供检测动物(例如马)是否易受C组链球菌生物感染的方法。

    Fluorometirc enzyme inhibition immunoassay for measuring potency of
allergen extracts
    88.
    发明授权
    Fluorometirc enzyme inhibition immunoassay for measuring potency of allergen extracts 失效
    荧光酶抑制免疫测定用于测定变应原提取物的效力

    公开(公告)号:US4528267A

    公开(公告)日:1985-07-09

    申请号:US476440

    申请日:1983-03-17

    摘要: An inhibition assay for measuring the potency of allergen extracts by incubating a mixture of allergen extract and reference allergen specific IgE in a buffered solution with an insoluble support to which reference allergen is adhered. The conjugated IgE adhering to the insoluble support is reacted with an enzyme labeled anti-IgE antibody and the enzyme label is contacted with a solution of a substrate which will yield a fluorescent product in the presence of the enzyme. The level of fluoresence in the solution is measured. The percentage of inhibition of the allergen specific IgE is determined from fluorescence levels measured for various extract concentrations.

    摘要翻译: 通过将缓冲溶液中的变应原提取物和参比变应原特异性IgE的混合物与参与变应原粘附的不溶性载体进行温育来测量变应原提取物的效力的抑制试验。 附着于不溶性载体的缀合的IgE与酶标记的抗IgE抗体反应,并且酶标记物与底物的溶液接触,所述底物将在酶的存在下产生荧光产物。 测量溶液中的荧光水平。 由各种提取物浓度测量的荧光水平确定变应原特异性IgE的抑制百分比。