p53 Recombinant Rabbit Monoclonal Antibody - BSA and Azide free [PSH03-95] (HA750920)

UNIPROT #

P02340

PROTEIN NAME

p53

SYNONYMS

Antigen NY-CO-13 antibody;BCC7 antibody;Cellular tumor antigen p53 antibody;FLJ92943 antibody;LFS1 antibody;Mutant tumor protein 53 antibody;p53 antibody;p53 tumor suppressor antibody;P53_HUMAN antibody;Phosphoprotein p53 antibody;Tp53 antibody;Transformation related protein 53 antibody;TRP53 antibody;Tumor protein 53 antibody;Tumor protein p53 antibody;Tumor suppressor p53 antibody

SUBCELLULAR LOCATION

Nucleus. Cytoplasm. Localized in both nucleus and cytoplasm in most cells. In some cells, forms foci in the nucleus that are different from nucleoli.

FUNCTION

Acts as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on the physiological circumstances and cell type. Involved in cell cycle regulation as a trans-activator that acts to negatively regulate cell division by controlling a set of genes required for this process. One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression. In cooperation with mitochondrial PPIF is involved in activating oxidative stress-induced necrosis; the function is largely independent of transcription. Induces the transcription of long intergenic non-coding RNA p21 (lincRNA-p21) and lincRNA-Mkln1. LincRNA-p21 participates in TP53-dependent transcriptional repression leading to apoptosis and seem to have to effect on cell-cycle regulation. Implicated in Notch signaling cross-over. Prevents CDK7 kinase activity when associated to CAK complex in response to DNA damage, thus stopping cell cycle progression. Isoform 2 enhances the transactivation activity of isoform 1 from some but not all TP53-inducible promoters. Isoform 4 suppresses transactivation activity and impairs growth suppression mediated by isoform 1. Isoform 7 inhibits isoform 1-mediated apoptosis. Regulates the circadian clock by repressing CLOCK-ARNTL/BMAL1-mediated transcriptional activation of PER2.