mSin3B Background Information It is now well established that Myc regulation of cell proliferation and differentiation involves a family of related transcription factors. One such factor, Max, is an obligate heterodimeric partner for Myc and can also form hetero-dimers with at least four related proteins designated Mad 1, Mxi 1 (alternatively designated Mad 2), Mad 3 and Mad 4. Like Mad 1 and Mxi 1, association of Mad 3 and Mad 4 with Max results in transcriptional repression. Both Myc and the Mad proteins have short half-lives and their synthesis is tightly regulated while Max expression is constitutive and relatively stable. Two related mammalian cDNAs have been identified and shown to encode Mad-binding proteins. Both possess sequence homology with the yeast transcription repressor Sin3 including four conserved paired amphipathic helix (PAH) domains. mSin3A and mSin3B specifically interact with the Mad proteins via their second paired amphipathic helix domain (PAH2). It has been suggested that Mad-Max heterodimers repress transcription by tethering mSin3 to DNA as corepressors.
mSin3B (A-20) Product Citations
See how others have used mSin3B (A-20): sc-996 antibody and or mSin3B (A-20) antibody conjugates.
8 total citations
Loading citations.
mSin3B (A-20)
Click on image to enlarge
mSin3B (A-20): sc-996. Immunoperoxidase staining of formalin-fixed, paraffin-embedded human lung tumor showing nuclear staining.
mSin3B (A-20): sc-996. Western blot analysis of mSin3B expression in HeLa nuclear extract.
mSin3B (A-20): sc-996. Western blot analysis of mSin3B expression in non-transfected: sc-117752 (A) and mouse mSin3B transfected: sc-121802 (B) 293T whole cell lysates.
mSin3B (A-20): sc-996. Western blot analysis of mSin3B expression in non-transfected: sc-117752 (A) and human mSin3B transfected: sc-116734 (B) 293T whole cell lysates.