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About Enzyme-Linked Immunosorbent Assay (ELISA)
The ELISA reaction relies on the specific interaction between antibodies and antigens. Wells in ELISA plates are coated with test-specific antigens. After a wash cycle removes excess and non-specifically bound antibodies, a secondary antibody with an enzyme detects the generated immune complex. Another wash cycle removes excess of the enzyme conjugate before a colorless substrate is added and converted into a colored product by the enzyme.
The color intensity is measured photometrically. It is proportional to the antibody activity in the sample. A standardized master curve is used for evaluation.
Some pathologies available on ELISA
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