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Radioimmunoassay - Radioimmunoassay is an extremely sensitive method for the detection and quantitation of any substance that is antigenic and that can be labelled with a radioactive isotope. Basically the method depends upon the competition between labelled (known) and unlabelled (unknown) antigen for the same antibody.

A known amount of labelled antigen (enzyme in this case), a known amount of specific antibody and an unknown amount of unlabelled antigen in the sample are allowed to reach equilibrium.

By measuring the amount of labelled antigen bound to the antibody, a measure of the antigen in unknown sample can be obtained. By suitably adjusting the amounts of antibody and labelled antigen, even small amount of antigen in an unknown material can be detected.

In order to measure the amount of labelled antigen attached to antibody, it is necessary to separate the antigen antibody complexes from the mixture. By measuring the radioactivity, the percentage of labelled antigen bound to the antibody can be calculated.

The concentration of an unknown (unlabelled) antigen can be determined by reference to a standard curve constructed from data obtained by allowing varying amounts of unlabelled antigen to compete