The developed method is an indirect competitive immunoassay designed to overcome these problems.
HAM1101 blood concentrations were quantified via competitive immunoassay employing chemoluminescence-labeled HAM1101 as tracer and ADM in the solid phase.
A competitive immunoassay between the antigen and the biotinylated hormone for the binding sites of the immobilized antibody was performed.
In addition, the mutants retained specific binding activity to anti-epitope antibodies, showing their potential utility in competitive immunoassay.
A competitive immunoassay format was employed to detect CA125 antigen with horseradish peroxidase (HRP) labeled CA125 antibody as tracer, o-phenylenediamine and hydrogen peroxide as enzyme substrates.
Based on a competitive immunoassay, benzo[a]pyrene, which can compete with the immobilized aminopyrene BSA in the association ability of the antibody, was successfully detected.
With a competitive immunoassay format, coated MC-LR competed for MC-LR antibody with added target MC-LR to form antibody-antigen immunocomplex.
In this competitive immunoassay system, PB acts as the redox mediator to reduce H2O2 originated from the catalyst cycle of GOD.
A popular technique in drug monitoring is competitive immunoassay for example ELISA which has proven to be simpler and less expensive.
With a competitive immunoassay format, the coated MC-LR antigen competed for MC-LR antibody with added target MC-LR to form antibody-antigen immunocomplex.
A competitive immunoassay format was adopted with horseradish peroxidase (HRP C3 as a tracer, hydroquinone and hydrogen peroxide as the enzymatic substrates.
