Course Content
Introduction to ELISA Testing
Learning Objectives By the end of this module, participants should be able to: Define ELISA and its purpose. Explain the principles behind antigen-antibody reactions. Understand the history and development of ELISA. Identify common applications of ELISA in clinical and research settings.
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Understanding ELISA Testing (Enzyme-Linked Immunosorbent Assay)

What is ELISA?

ELISA (Enzyme-Linked Immunosorbent Assay) is a laboratory technique used to detect and quantify antigens or antibodies in biological samples.

The test relies on the highly specific binding between antigens and antibodies.


Basic Principle

The ELISA process involves:

  1. Coating
    • Antigen or antibody is attached to a microplate well.
  2. Blocking
    • Unoccupied sites are blocked to prevent nonspecific binding.
  3. Sample Addition
    • Patient sample is added.
  4. Detection Antibody Addition
    • Enzyme-linked antibody binds to the target.
  5. Washing
    • Removes unbound materials.
  6. Substrate Addition
    • Enzyme reacts with substrate to produce color.
  7. Measurement
    • Color intensity is measured using an ELISA reader.

The amount of color produced is proportional to the concentration of the target analyte.