Information about ELISA
The Enzyme Linked Immuno-Sorbent Assay or ELISA is a method commonly employed in biochemistry to detect if a certain substance is present in a sample. It employs antibody specific to the substance; these antibody are linked to an enzyme which produces a signal. The steps of the general ELISA test are as follows: 1. Apply the sample to some sticky substrate, usually a plate with wells. 2. Apply the enzyme-linked antibody and let it bind to the substance. 3. Wash the plate, so that unbound antibody is removed. 4. Apply a chemical which is converted by the enzyme into a fluorescent signal. 5. View the result: if it fluoresces, then the sample contained the substance. The enzyme acts as an amplifier: even if only few enzyme-linked antibody are present, the enzyme molecules will produce many fluorescent signal molecules. A variant of this techniqe is used in medicine to detect if a person's blood contains antibody against a certain antigen (which would indicate infection). The initial screening test for HIV infection is such an ELISA test. The steps are as follows: 1. Prepare a plate to which the antigen is bound 2. Apply the human serum to be tested 3. Wash the plate, so that unbound antibody is removed. 4. Apply an enzyme-linked antibody which specifically binds to human antibody. 5. Wash the plate, so that the unbound enzyme-linked antibody is removed. 6. Apply a chemical which is converted by the enzyme into a fluorescent signal. 7. View the result: if it fluoresces, then the serum sample contained antibody against the antigen.
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