Thromb Haemost 1987; 57(02): 212-216
DOI: 10.1055/s-0038-1651096
Original Article
Schattauer GmbH Stuttgart

Identification of Platelet Antigens by Monoclonal Antibodies Using Crossed Immunoelectrophoresis with Immunoblotting of the Monoclonal Antibody

L I Thorsen
Research Institute for Internal Medicine, Rikshospitalet, University of Oslo, Oslo
,
G Gaudernack
*   Institute of Transplantation Immunology, Rikshospitalet, University of Oslo, Oslo
,
F Brosstad
Research Institute for Internal Medicine, Rikshospitalet, University of Oslo, Oslo
,
T M Pedersen
Research Institute for Internal Medicine, Rikshospitalet, University of Oslo, Oslo
,
N O Solum
Research Institute for Internal Medicine, Rikshospitalet, University of Oslo, Oslo
› Author Affiliations
Further Information

Publication History

Received 28 October 1986

Accepted after revision 27 January 1987

Publication Date:
28 June 2018 (online)

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Summary

A method is described for the identification of antigens by monoclonal antibodies. This is applicable whenever precipitating antibodies to the same antigens from a different species are available. The method is based upon: 1) Separation and immunoprécipitation of cellular proteins with a polyspecific antiserum in crossed immunoelectrophoresis in the presence of the non-denaturing detergent Triton X-100 and the monoclonal antibody. 2) Coprecipitation of the monoclonal antibody with its antigen. 3) Subsequent passive transfer of the monoclonal antibody in the antibody-antigen complex onto a nitrocellulose membrane. 4) Visualization of the blotted antibody using an enzyme-linked secondary antibody and a chromogenic substrate. 5) Identification of the corresponding antigen by comparisons to the immunoprecipitate pattern of the original immunoplate. To test this method we have analyzed the detection of the antigens recognized by six previously described monoclonal antibodies against platelet membrane proteins and von Willebrand factor. Specific immunoblots were obtained in each case using small amounts of monoclonal antibodies. Thus, the technique provides an alternative when epitopes are denatured by SDS, and avoids the use of radioactively labelled monoclonal antibodies.