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You are viewing a stripped-down version of this page without the latest data files. This site may not be updated by NACE, Inc. Page last updated 11/06/10.
You are viewing a stripped-down version of this page without the latest data files. This site may not be updated by NACE, Inc. Page last updated 11/06/10.
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Expression of human c-MYC, the oncogene that controls the growth of various human tumors, is often related to amplification of the c-MYC gene in tumors. To examine whether MYC mRNA is translated to a full-length protein and whether this protein forms a dimer that is bioactive, we made a polyclonal antibody against a synthetic peptide that represents residues around the amino-terminal region of an human MYC protein. We found that this antibody recognized a 14-kDa protein in HeLa cells and in a T-47D adenocarcinoma cell line, both of which express abundant levels of c-MYC mRNA, but not in another cell line, the T-24 bladder carcinoma cell line. This protein was not present in T-47D cells in which c-MYC expression was repressed by a c-MYC short interfering RNA. The 14-k
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