Enzyme-linked immunosorbent assay (ELISA) is a method of target antigen (or antibody) capture in samples using a specific antibody (or antigen), and of target molecule detection/quantitation using an enzyme reaction with its substrate.
In ELISA, various antigen-antibody combinations are used, always including an enzyme-labeled antigen or antibody, and enzyme activity is measured colorimetrically.
The enzyme activity is measured using a substrate that changes color when modified by the enzyme. Light absorption of the product formed after substrate addition is measured and converted to numeric values.
Depending on the antigen-antibody combination, the assay is called a direct ELISA, indirect ELISA, sandwich ELISA, competitive ELISA etc.
A target protein (or a target antibody) is immobilized on the surface of microplate wells and incubated with an enzyme-labeled antibody to the target protein (or a specific antigen to the target antibody). After washing, the activity of the microplate well-bound enzyme is measured.
A target protein is immobilized on the surface of microplate wells and incubated with an antibody to the target protein (the primary antibody), followed by a secondary antibody against the primary antibody. After washing, the activity of the microplate well-bound enzyme is measured.
Although indirect ELISA requires more steps than direct ELISA, labeled secondary antibodies are commercially available, eliminating the need to label the primary antibody.
An antibody to a target protein is immobilized on the surface of microplate wells and incubated first with the target protein and then with another target protein-specific antibody, which is labeled with an enzyme. After washing, the activity of the microplate well-bound enzyme is measured. The immobilized antibody (orange) and the enzyme-labeled antibody (green) must recognize different epitopes of the target protein.
An antibody specific for a target protein is immobilized on the surface of microplate wells and incubated with samples containing the target protein and a known amount of enzyme-labeled target protein.
After the reaction, the activity of the microplate well-bound enzyme is measured.
When the antigen level in the sample is high, the level of antibody-bound enzyme-labeled antigen is lower and the color is lighter. Conversely, when it is low, the level of antibody-bound enzyme-labeled antigen is higher and the color, darker. The graph above and to the right illustrates the correlation between absorption and antigen levels in samples.
Immobilization is commonly mediated by hydrophobic interaction or covalent bonds.
Microplates that are pre-activated for different immobilization methods are commercially available. The choice of method of immobilization depends on the type of protein to be immobilized. In general, covalent bonding is preferred for smaller molecules, such as peptides, and hydrophobic interaction (physical adsorption) is preferred for larger molecules, such as proteins. An appropriate method should be determined for each assay system.
Many types of ELISA microplates are commercially available, including the hydrophobic type, hydrophilic type as well as types surface-activated with amino or carboxyl groups. Surface-activated microplates are useful for covalent bonding.
It is important to select the correct type of ELISA microplate for the intended use.
|Preparation of reagents and equipment|
|Immobilization of antibody
Add diluted antibody to each well of a 96-well ELISA plate. Seal the plate to prevent evaporation, and allow it to incubate at 4°C for 15-18 hours to immobilize the antibody.
Remove the diluted antibody, and wash 3 times with washing solution.
Add blocking buffer to each well, and allow it to incubate at 37°C for 1 hour to reduce non-specific binding of the target protein to the well.
Remove the blocking buffer, and wash 3 times with washing solution.
| Addition of samples
Dilute the samples with sample dilution buffer, and add 100 µL of each sample to each well. For the calibration curve, prepare a dilution series of the standard on the same plate. Allow it to incubate at 37°C for 1 hour.
Remove the samples, and wash 5 times with washing solution.
|Addition of the detection antibody
Dilute the detection antibody in sample dilution buffer, and add 100 µL to each well.
Allow it to incubate at 37°C for 1 hour.
After reaction, remove the detection antibody, and wash 5 times with washing solution.
|Addition of enzyme-labeled secondary antibody
Dilute an enzyme-labeled secondary antibody with sample dilution buffer, and add 100 µL to each well.
Allow it to incubate at 37°C for 1 hour.
After reaction, remove the secondary antibody, and wash 5 times with washing solution.
|Add a substrate solution.
Allow it to incubate as the color develops.
|Add a stop solution to stop the reaction when the color is sufficiently developed.
|Measure the absorption at 450 nm by a plate reader.|
|Antibodies suitable for ELISA
||List of primary antibodies
List of secondary antibodies
|ELISA kits||Kits to make sandwich ELISA: Ab-Match Kits
ELISA kits and related products for drug discovery
ELISA kits and related products for metabolism research
|When Blocking||Bovine Serum Albumin Reagent Grade Powder (pH7.0)|