METHOD AND KIT FOR PERFORMING NUCLEIC ACID HYBRIDIZATION ASSAYS
    31.
    发明公开
    METHOD AND KIT FOR PERFORMING NUCLEIC ACID HYBRIDIZATION ASSAYS 失效
    程序核酸的试验杂交实现。

    公开(公告)号:EP0227795A1

    公开(公告)日:1987-07-08

    申请号:EP86904513.0

    申请日:1986-06-13

    Abstract: Un procédé et un kit d'isolement et de détection quantitative dans une solution d'une séquence sélectionnée d'acide nucléique cible comprennent deux agents d'investigation. Un premier agent d'investigation est complémentaire d'une partie de la cible et est attaché de manière covalente à un premier complexant (un antigène ou un anticorps, par exemple). Le deuxième agent d'investigation est complémentaire d'une partie différente de la cible et est associé à un groupe rapporteur. Apès l'hybridation de la cible et des deux agents d'investigation dans la solution, on utilise un support solide enduit d'un deuxième complexant (un anticorps ou un antigène correspondants, par exemple) capable de se lier au premier complexant sur le premier agent d'investigation afin d'immobiliser le composé hybride de cible et d'agent d'investigation. Le premier agent d'investigation utilisé peut appartenir à plusieurs types différents. Chaque type s'attache au même genre de complexant mais comprend une séquence d'acides nucléiques complémentaire d'une partie différente de la cible.

    CYANIDE-FREE REAGENT AND METHOD FOR THE DETERMINATION OF HEMOGLOBIN
    33.
    发明授权
    CYANIDE-FREE REAGENT AND METHOD FOR THE DETERMINATION OF HEMOGLOBIN 失效
    氰化物试剂和方法用于确定血红蛋白

    公开(公告)号:EP0749583B1

    公开(公告)日:2002-08-28

    申请号:EP95912800.0

    申请日:1995-03-06

    Abstract: A cyanide-free method and reagent for determining the concentration of total hemoglobin in a whole blood sample accurately in less than 10 seconds comprising a ligand selected from the group consisting of imidazole, imidazole derivatives, N-hydroxyacetamide, N-hydroxyl amine, pyridine, oxazole, thiazole, pyrazole, pyrimidine, purine, quinoline, and isoquinoline, and a surfactant with strong erythrolytic capability selected from the group consisting of lauryl dimethylamine oxide and octylphenoxy polyethoxyethanol. The reagent pH is adjusted to about 11 to about 14. Rapid mixing of the reagent with a blood sample leads to the formation of a stable chromogen whose absorbance can be measured between 540 and 550 nm. The cyanide-free reagent is ideal for use on an automated high through-put clinical hematology analyzer.

    METHOD FOR PERFORMING NUCLEIC ACID HYBRIDIZATION ASSAYS
    40.
    发明授权
    METHOD FOR PERFORMING NUCLEIC ACID HYBRIDIZATION ASSAYS 失效
    程序核酸的试验杂交实现

    公开(公告)号:EP0227795B2

    公开(公告)日:2002-07-24

    申请号:EP86904513.8

    申请日:1986-06-13

    Abstract: A method and a kit for the isolation and quantitative detection of a selected target nucleic acid sequence from solution employing two probes. A first probe is complementary to one portion of the target and is covalently attached to a first complexing agent (e.g., either an antigen or an antibody). The second probe is complementary to a different portion of the target and is associated with a reporter group. Following hybridization of the target and two probes in solution, a solid support coated with a second complexing agent (i.e., a corresponding antibody or antigen) capable of binding to the first complexing agent on the first probe is employed to immobilize the target-probe hybrid complex. A plurality of types of first probes may be used. Each type is attached to the same sort of complexing agent but each includes a nucleic acid sequence which is complementary to a different portion of the target.

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