A test sample is added to a beaker.
It is washed to removed any unbound test samples.
An antibody complementary in shape to the antigen being tested for is added.
It is washed to remove unbound antibodies.
A second antibody, complementary to the first antibody, is added. It has an enzyme attached. Rinsed again.
A colourless substrate for the enzyme is added. This will produce colourful products in the presence of the enzyme.
The presence of this colour indicates the presence of the antigen.
More intense colour= more antigens.