Group-selective immunoassay

A new solid-phase immunoassay technique has been applied for anti-digoxin monoclonal antibodies (Mabs) detection. At the first assay step, anti-digoxin Mabs (IgG1, K aff = 9.2 × 10 9 M −1) were bound to a specially prepared immunosorbent, the microtiter plates coated with digoxin-human serum albumin...

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Veröffentlicht in:Immunology letters 1994-07, Vol.41 (2), p.235-239
Hauptverfasser: Yazynin, Sergey A., Deyev, Sergey M.
Format: Artikel
Sprache:eng
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Zusammenfassung:A new solid-phase immunoassay technique has been applied for anti-digoxin monoclonal antibodies (Mabs) detection. At the first assay step, anti-digoxin Mabs (IgG1, K aff = 9.2 × 10 9 M −1) were bound to a specially prepared immunosorbent, the microtiter plates coated with digoxin-human serum albumin conjugate (Dig-HSA), in which free amino groups were protected by a glutaraldehyde cross-linking modification. The modification did not essentially influence the antibody-binding capacity of the immunosorbent. After antigen-antibody reaction, free amino groups were located only on the anti-digoxin Mabs, bound to chemically modified immunosorbent. At the second assay step, free amino groups of anti-digoxin Mabs were biotinylated by N-hydroxysuccinimide-biotin ester. Then the biotin residues were detected by the streptavidin-peroxidase conjugate. The method does not require second labeled antibodies and may be used for anti-hapten hybridoma screening.
ISSN:0165-2478
1879-0542
DOI:10.1016/0165-2478(94)90139-2