| Literature DB >> 31267495 |
Linda M Murungi1, Rinter K Kimathi2, James Tuju2,3, Gathoni Kamuyu4, Faith H A Osier2,4.
Abstract
The enzyme-linked immunosorbent assay (ELISA) is a reliable and relatively low-cost method for measuring soluble ligands such as antibodies and proteins in biological samples. For analysis of specific antibodies in serum, a capture antigen is immobilized onto a solid polystyrene surface from which it can capture the antibodies. The captured antibodies are subsequently detected using a secondary antibody conjugated to an enzyme. Detection is accomplished by addition of a colorimetric substrate, and the readout is absorbance (optical density). Here, we provide a detailed standardized ELISA protocol for the quantification of antibodies against malaria antigens.Entities:
Keywords: Antibodies; Antigens; ELISA; Optical density; Serum
Mesh:
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Year: 2019 PMID: 31267495 PMCID: PMC7613324 DOI: 10.1007/978-1-4939-9550-9_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745