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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.

More information Original publication

DOI

10.1007/978-1-4939-9550-9_6

Type

Journal article

Publication Date

2019-01-01T00:00:00+00:00

Volume

2013

Pages

83 - 90

Total pages

7

Addresses

K, E, M, R, I, , W, e, l, l, c, o, m, e, , T, r, u, s, t, , R, e, s, e, a, r, c, h, , P, r, o, g, r, a, m, m, e, ,, , C, e, n, t, r, e, , f, o, r, , G, e, o, g, r, a, p, h, i, c, , M, e, d, i, c, i, n, e, , R, e, s, e, a, r, c, h, -, C, o, a, s, t, ,, , K, i, l, i, f, i, ,, , K, e, n, y, a, ., , L, M, u, r, u, n, g, i, @, k, e, m, r, i, -, w, e, l, l, c, o, m, e, ., o, r, g, .

Keywords

Humans, Malaria, Antibodies, Antigens, Antimalarials, Enzyme-Linked Immunosorbent Assay