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Immunoprecipitation with MT.M MAbs from lysates of vectorially iodinated MT2 cells. MT2 cells were surface labeled with 125I, and immunoprecipitation analysis was carried out as described in Materials and Methods. In this experiment, the cell lysate was not precleared with normal rabbit serum and SaC. Control antibodies used were anti-CD54 (84H10), anti-CD18 (H52), and isotype-matched myeloma protein (IgG1). Migration positions of molecular weight standards are indicated.
