Misplaced Pages

ELISA: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editNext edit →Content deleted Content addedVisualWikitext
Revision as of 18:34, 29 September 2002 edit163.28.80.22 (talk)No edit summary← Previous edit Revision as of 02:10, 30 September 2002 edit undoAxelBoldt (talk | contribs)Administrators44,502 editsNo edit summaryNext edit →
Line 1: Line 1:
ELISA stands for ] Linked Immuno-Sorbent Assay. Essentially, this assay tells you if there is a certain ] in any given sample. The steps in this procedure are: The '''Enzyme Linked Immuno-Sorbent Assay''' or '''ELISA''' is a method commonly employed in ] to detect if a certain ] is present in a given sample. The steps in this procedure are:

1) Attach an ] (this ] specifically binds to the ] of interest) to a solid support (usually a membrane)
2) Apply the sample to this membrane, and let the ] bind to the ] # Create an ] which specifically binds to the protein of interest.
# Attach this antibody to a solid support (usually a membrane) .
3) Wash the membrane
# Apply the sample to this membrane, and let the protein bind to the antibody.
4) Apply a second ] which is linked to an ]
# Wash the membrane, so that only the proteine bound to the antibody remains.
5) Apply a chemical which is coverted by the ] into a flourescent signal
# Apply a second antibody which is linked to an ] and binds to the proteine of interest.
6) See the result
# Apply a chemical which is coverted by the enzyme into a flourescent signal.
# View the result


Any basic ] or ] textbook should have more information. Any basic ] or ] textbook should have more information.

Revision as of 02:10, 30 September 2002

The Enzyme Linked Immuno-Sorbent Assay or ELISA is a method commonly employed in biochemistry to detect if a certain protein is present in a given sample. The steps in this procedure are:

  1. Create an antibody which specifically binds to the protein of interest.
  2. Attach this antibody to a solid support (usually a membrane) .
  3. Apply the sample to this membrane, and let the protein bind to the antibody.
  4. Wash the membrane, so that only the proteine bound to the antibody remains.
  5. Apply a second antibody which is linked to an enzyme and binds to the proteine of interest.
  6. Apply a chemical which is coverted by the enzyme into a flourescent signal.
  7. View the result

Any basic immunology or molecular biology textbook should have more information. Try http://www.ncbi.nlm.nih.gov. They got books.