Flow Cytometric Analysis of PFA-fixed HeLa cells. MXI1 Mouse Monoclonal Antibody (PCRP-MXI1-1A3) followed by goat anti-mouse IgG-CF488 (blue); unstained cells (red).
Immunofluorescence analysis of PFA-fixed HeLa cells. MXI1 Mouse Monoclonal Antibody (PCRP-MXI1-1A3)
SDS-PAGE Analysis Purified MXI1 Mouse Monoclonal Antibody (PCRP-MXI1-1A3). Confirmation of Purity and Integrity of Antibody.
Analysis of Protein Array containing more than 19,000 full-length human proteins using MXI1 Mouse Monoclonal Antibody (PCRP-MXI1-1A3).
Known Applications & Suggested Dilutions
Host / Ig Isotype
Mol. Weight of Antigen
Specificity & Comments
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 heterodimers with at least four related proteins designated Mad 1, Mxi1 (also designated Mad 2), Mad 3 and Mad 4. Like Mad 1 and Mxi1, 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.