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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This section contains information intended for wide distribution and may therefore contain product details or information that is not available or valid in your country. Please contact your local Sebia representative. Information intended for healthcare professionals. Carefully read the instructions in the reagent package inserts and instrument manuals.
