AffiELISA® Pan ADT Kit: Max Sensitivity Androsterone ELISA Detection

The AffiELISA® Pan ADT Kit uses competitive inhibition enzyme immunoassay technique. The provided microtiter plate comes pre-coated with Androsterone (ADT) protein. To perform the assay, standards or samples are added to designated wells on the microtiter plate. Subsequently, a biotin-conjugated antibody specific to Androsterone (ADT) is introduced. Avidin conjugated to Horseradish Peroxidase (HRP) is then added to each well, followed by an incubation period. Afterward, the TMB substrate solution is added, initiating an enzyme-substrate reaction. To conclude the reaction, a sulphuric acid solution is introduced, causing a color change that can be measured spectrophotometrically at a wavelength of 450nm ± 10nm. By comparing the optical density (OD) of the samples to the standard curve, the concentration of Androsterone (ADT) in the samples can be determined.