QuantiGlo| QuantiGlo® ELISA Assay Principle
QuantiGlo® ELISA Assay Principle

Step 1

Step 2

A microplate pre-coated with capture antibody is provided. Samples or standards are added and any analyte present is bound by the immobilized antibody. Unbound materials are washed away.

A second HRP-labeled antibody (detection antibody) is added and binds to the captured analyte. Unbound detection antibody is washed away.

Step 3

Legend
Enhanced Luminol substrate is added and light is produced in proportion to the amount of analyte present in the sample. A microplate luminometer is used to measure the intensity of the light emitted.