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The '''Enzyme-Linked Immunosorbent Assay''' ('''ELISA''' or '''EIA''' for short) is a method usually employed in ] to detect if a certain substance is present in a ]. It utilizes ] ] to the substance; these antibodies are linked to an ] which causes a chromogenic substrate to produce a ]. The '''Enzyme-Linked Immunosorbent Assay''' ('''ELISA''' or '''EIA''' for short) is a method usually employed in ] to detect the presence of a certain substance in a ]. It utilizes ] ] to the substance (]); these antibodies are linked to an ] which causes a chromogenic or fluorogenic substrate to produce a ].


The steps of the general ELISA test are: The steps of the general, non-competitive ELISA are:
# Apply the sample to some sticky substrate, usually a plate with wells. # Apply the sample to some sticky substrate, usually a plate with wells.
# Apply the enzyme-linked antibodies and let them bind to the substance. # Apply the enzyme-linked antibodies and let them bind to the substance.
# Wash the plate, so that unbound antibodies are removed. # Wash the plate, so that unbound antibodies are removed.
# Apply a chemical which is converted by the enzyme into a ] signal. # Apply a which is converted by the enzyme into a ] signal.
# View the result: if it fluoresces, then the sample contained the substance. # View the result: if it fluoresces, then the sample contained the substance.


The enzyme acts as an amplifier: even if only few enzyme-linked antibodies are present, the enzyme molecules will produce many fluorescent signal molecules. The enzyme acts as an amplifier: even if only few enzyme-linked antibodies are present, the enzyme molecules will produce many fluorescent signal molecules.

ELISA may be run in a qualitative or quantitative format. Qualitative results provide a simple positive or negative result for a sample. The cutoff between positive and negative is determined by the analyst. In quantitative ELISA, the optical density or fluorescent units of the sample is interpolated into a standard curve which is typically a serial dilution of the target.


A variant of this technique is used in ] to detect if a person's ] contains antibodies against a certain ] (which would indicate past or present infection). The initial ] is such an ELISA test. The steps are as follows: A variant of this technique is used in ] to detect if a person's ] contains antibodies against a certain ] (which would indicate past or present infection). The initial ] is such an ELISA test. The steps are as follows:

Revision as of 18:57, 23 May 2005

For the artificial intelligence program, see ELIZA

The Enzyme-Linked Immunosorbent Assay (ELISA or EIA for short) is a method usually employed in biochemistry to detect the presence of a certain substance in a sample. It utilizes antibodies specific to the substance (antigen); these antibodies are linked to an enzyme which causes a chromogenic or fluorogenic substrate to produce a signal.

The steps of the general, non-competitive ELISA are:

  1. Apply the sample to some sticky substrate, usually a plate with wells.
  2. Apply the enzyme-linked antibodies and let them bind to the substance.
  3. Wash the plate, so that unbound antibodies are removed.
  4. Apply a 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 antibodies are present, the enzyme molecules will produce many fluorescent signal molecules.

ELISA may be run in a qualitative or quantitative format. Qualitative results provide a simple positive or negative result for a sample. The cutoff between positive and negative is determined by the analyst. In quantitative ELISA, the optical density or fluorescent units of the sample is interpolated into a standard curve which is typically a serial dilution of the target.

A variant of this technique is used in medicine to detect if a person's blood contains antibodies against a certain antigen (which would indicate past or present 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 antibodies are removed.
  4. Apply the enzyme-linked antibodies which specifically bind to the human antibodies.
  5. Wash the plate, so that unbound enzyme-linked antibodies are 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 antibodies against the antigen.

See also:

External links

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