Enzyme-linked immunoassay (ELISA) for connective tissue components

SI Rennard, R Berg, GR Martin, JM Foidart… - Analytical …, 1980 - Elsevier
SI Rennard, R Berg, GR Martin, JM Foidart, PG Robey
Analytical Biochemistry, 1980Elsevier
Enzyme-linked immunoadsorbant assays have been developed for types I, II, III, and IV
collagen and for laminin and fibronectin. These assays offer a specific, sensitive, and
convenient method for the measurement of various connective tissue components either
separately or simultaneously. Plastic microtiter wells are coated with purified antigen, then
antibodies to the antigen are allowed to bind to the insolubilized antigen in each well. The
amount of bound antibody is determined by incubation with a second antibody which is …
Enzyme-linked immunoadsorbant assays have been developed for types I, II, III, and IV collagen and for laminin and fibronectin. These assays offer a specific, sensitive, and convenient method for the measurement of various connective tissue components either separately or simultaneously. Plastic microtiter wells are coated with purified antigen, then antibodies to the antigen are allowed to bind to the insolubilized antigen in each well. The amount of bound antibody is determined by incubation with a second antibody which is covalently linked to alkaline phosphatase or horseradish peroxidase. The amount of bound enzyme is assayed after adding an appropriate substrate. The level of protein in a sample is estimated from its ability to inhibit the binding of the first antibody to the antigen-coated well. Specificity of the assay depends on the purity of the adsorbed antigen and allows for highly specific tests. Under optimum conditions the sensitivity of the assay is determined by the KB of the antibody and allows 10–20 ng of a specific type of collagen or laminin and 1 ng fibronectin to be detected.
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