Final answer:
To detect antibodies against bacteria using an EIA, you need to attach antigen from the bacteria to the wells of a microtiter plate. Then add a marker-specific antibody, wash the support, add a second antibody that binds specifically to the primary antibody, and finally add a colorless substrate that is converted to a colored product only if the specific antigen is present. The color intensity can be measured using a spectrophotometer.
Step-by-step explanation:
- Attach antigen from the bacteria to the wells of a microtiter plate
- Add marker-specific antibody (primary antibody) to the bound material
- Wash the support to remove unbound primary antibody
- Add a second antibody (secondary antibody) that binds specifically to the primary antibody
- Add a colorless substrate that is converted to a colored product only if the specific antigen is present
- Measure the color intensity using a spectrophotometer