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Immunoenzymometric assay

Freytag, J.W., Lau, H.P., and Wadsley, J.J. (1984a) Affinity-column-mediated immunoenzymometric assays Influence of affinity-column ligand and valency of antibody-enzyme conjugates. Gun. Chem. 30, 1494-1498. [Pg.1064]

M7. Miyai, K., Ishibashi, K., and Kawashima, M., Two-site immunoenzymometric assay for thyrotropin in dried blood samples on filter paper. Clin. Chem. 27, 1421-1423 (1981). [Pg.107]

Rabitzsch G, Mair J, Lechleitner P, Noll F, Hofmann U, Krause EG, et al. Immunoenzymometric assay of human glycogen phosphorylase isoenzyme BB in diagnosis of ischemic myocardial injury. Clin Chem 1995 41 966-78. [Pg.641]

Chan DW, Kelsten M, Rock R, Bruzek D. Evaluation of a monoclonal immunoenzymometric assay for alpha-fetoprotein. Clin Chem 1986 32 1318-22. [Pg.788]

Townsend JC. A competitive immunoenzymometric assay for albumin in urine. Chn Chem 1986 32 1372-4. [Pg.900]

Vieira J, Lombardi M, Nishida S. Monoclonal antibody-based immunoenzymometric assay for serum human growth hormone. Braz J Med Biol Res 1990 23 293-6. [Pg.2001]

Methods based on radiolabels continue to hold an important place in routine analysis and in research related to clinical testing. The main techniques included in this group are radioimmunoassy (RIA), immunoradiometric assay (IRMA), and scintillation proximity assay (SPA). Many researchers in this field use short-lived radioisotopes and chelating agents in antibody labeling.139 The most popular types of immunoassay are methods that use enzymatic labels the enzyme-linked immunosorbent assay (ELISA), the enzyme-monitored immunotest (EMIT), the competitive binding enzyme immunoassay (EIA), and the immunoenzymometric assay (IEMA). [Pg.46]

Homogenous immuno-radiometric assay (IRMA) Homogenous immunoenzymometric assay (lEMA)... [Pg.645]

Immunoenzymometric assay was performed with microtiter plates as a solid-phase antibody and enzyme-labeled antibodies as conjugate (Fig. 1). Lipoprotein particles react first with immobilized antibody 1. Unbound particles are removed by washing and excess of enzyme labeled antibody 2 is allowed to react with bound antigen. Unbound labeled antibodies are removed by washing and solid phase bound enzyme is measured. The different steps have been automatized in our laboratory. [Pg.19]

Monoclonal antibodies can be used as first antibody in our immunoenzymometric assay. As any single epitope of an apolipoprotein may be more or less exposed depending on which particle one is examining, monoclonal antibodies can separate lipoproteins that may be similar by physicochemical criteria. [Pg.23]

See other pages where Immunoenzymometric assay is mentioned: [Pg.139]    [Pg.143]    [Pg.2129]    [Pg.10]    [Pg.645]    [Pg.222]    [Pg.139]    [Pg.143]    [Pg.2129]    [Pg.10]    [Pg.645]    [Pg.222]   
See also in sourсe #XX -- [ Pg.143 ]



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