Assay method employing fluorescent cell incorporative dye
    1.
    发明授权
    Assay method employing fluorescent cell incorporative dye 失效
    使用荧光细胞融合染料的测定方法

    公开(公告)号:US4748129A

    公开(公告)日:1988-05-31

    申请号:US645458

    申请日:1984-08-28

    摘要: A method is provided for determining the presence in a sample of a member of a specific binding pair ("sbp member") consisting of ligand and its homologous receptor. The sample is combined in an aqueous medium with (1) a complementary sbp member wherein at least the sbp member or the complementary sbp member is bound to the surface of a cell and (2) a fuorescent agent capable of being incorporated into the cell. The presence of the sbp member is indicated by a change in fluorescence of the unseparated cell suspension as a result of agglutination of the cells.The present invention has particular application to blood typing, for example, for the determination of the presence of blood group antigens A, B, AB, O, and D (Rh.sub.o) and antibodies to such antigens.

    摘要翻译: 提供了一种用于确定由配体及其同源受体组成的特异性结合对(“sbp成员”)的成员的样品中存在的方法。 样品在水性介质中与(1)互补sbp构件组合,其中至少sbp构件或互补sbp构件与细胞表面结合,和(2)能够结合到细胞中的荧光剂。 由于细胞凝集,未分离的细胞悬浮液的荧光变化表示sbp成员的存在。 本发明特别适用于血型分型,例如用于测定血型抗原A,B,AB,O和D(Rho)及其抗体的存在。

    Heterogeneous binding assays
    4.
    发明授权
    Heterogeneous binding assays 失效
    异质结合试验

    公开(公告)号:US5437983A

    公开(公告)日:1995-08-01

    申请号:US13116

    申请日:1993-02-01

    摘要: A method for carrying out a binding assay is described wherein a member of a specific binding pair (sbp) and a sample are combined with a matrix of non-porous beads in a liquid medium under conditions such that the beads bind to the sbp member. The liquid medium is removed from the beads by aspiration using an aspiration tube having one or more orifices each of a diameter smaller than the minimum diameter of the smallest bead thereby allowing removal of the liquid medium while prohibiting aspiration of the beads.

    摘要翻译: 描述了一种用于进行结合测定的方法,其中将特定结合对(sbp)和样品的成员与液体培养基中的无孔珠粒基质结合,使得珠子与sbp构件结合。 通过使用具有一个或多个直径小于最小珠的最小直径的孔的抽吸管通过抽吸将液体培养基从珠粒中除去,从而允许除去液体培养基,同时禁止吸入珠粒。