Characterization by Scatchard plots of monoclonal antibody enzyme conjugates directed against alpha-1-foetoprotein

A radioimmunoassay was used to investigate the affinity of 2 monoclonal antibodies against human alpha-1-foetoprotein before and after conjugation with horseradish peroxidase. The equilibrium constant of the high-affinity antibody was reduced 10-fold whereas it remained unaffected in the low-affinit...

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Veröffentlicht in:Journal of immunological methods 1984-02, Vol.66 (2), p.277-284
Hauptverfasser: Porstmann, T., Porstmann, Baerbel, Micheel, B., Schmidt, E.-H., Herzmann, H.
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Sprache:eng
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Zusammenfassung:A radioimmunoassay was used to investigate the affinity of 2 monoclonal antibodies against human alpha-1-foetoprotein before and after conjugation with horseradish peroxidase. The equilibrium constant of the high-affinity antibody was reduced 10-fold whereas it remained unaffected in the low-affinity antibody. With the Scatchard diagram, quantification of unlabelled antibodies in the unpurified conjugate mixture is also possible if antibody affinity is changed by the coupling procedure.
ISSN:0022-1759
1872-7905
DOI:10.1016/0022-1759(84)90339-9