The principle of the following enzyme immunoassay test follows the typical competitive binding scenario. Competition occurs between an unlabeled antigen (present in calibrators, control and patient samples) and an enzyme-labelled antigen (conjugate) for a limited number of antibody binding sites on the microwell plate.

The washing and decanting procedures remove unbound materials. After the washing step, the enzyme substrate is added. The enzymatic reaction is terminated by addition of the stopping solution. The absorbance is measured on a microtiter plate reader.

The intensity of the colour formed is inversely proportional to the concentration of fT4 in the sample. A set of calibrators is used to plot a calibration curve from which the amount of fT4 in patient samples and controls can be directly read.

The labeled T4 (conjugate) employed in this assay system has shown no binding properties towards thyroxine-binding globulin (TBG) and human serum albumin (HSA). The binding sites on the microwell plates are designed to be of a low binding-capacity in order not to disturb the equilibrium between T4 and its carrying proteins.

The assay is carried out under normal physiological conditions of pH, temperature and ionic strength.

Hey, it seems that you’re connected from United States.

For registration requirements in countries outside of European market, please contact regulatory.affairs@diasource.be.