
A transplantable murine breast tumor antigen (called JC tumor) has been recognized by the detection of McAb F36/22 with the method of immunoblotting. JC tumor antigen was isolated by Sepharose-CL-4B, then was purified by McAb F36/22 affinity chromatography. Solid phase RIA detection demonstrated that the specific activity of the antigen which was purified by 188.4 times was 148,000 cpm/mg protein. SDS-PAGE and immunoblot analysis revealed that the tumor antigen possessed a molecular weight of 60kd. Competitive binding RIA indicated that JC tumor antigen inhibited the combining of ductal carcinoma antigen with McAb F36/22. It implied that some groups (antigen determinant) on JC tumor antigen were the same as or similar to those on ductal cancer antigen.
Epitopes, Mice, Mice, Inbred BALB C, Antigens, Neoplasm, Immunoblotting, Radioimmunoassay, Animals, Antibodies, Monoclonal, Mammary Neoplasms, Experimental, Chromatography, Affinity
Epitopes, Mice, Mice, Inbred BALB C, Antigens, Neoplasm, Immunoblotting, Radioimmunoassay, Animals, Antibodies, Monoclonal, Mammary Neoplasms, Experimental, Chromatography, Affinity
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