Phospho-p53-S392 Rabbit pAb

P53 is a tumor suppressor that plays a role in maintaining genomic stability and controlling apoptosis. During the cell cycle, it can arrest cells at the G1/S checkpoint and activate DNA repair mechanisms. It is the most mutated gene in cancer. In unstressed cells, p53 usually exists at low levels in an inactive form, being bound to Mdm2. Phosphorylation of p53 at Ser392 is increased in human tumors and has been reported to influence the growth suppressor function, DNA binding, and transcriptional activation of p53.

Additional Information

Product Name: Phospho-p53-S392 Rabbit pAb
Catalog No.: Z4152-100
Also Known As: TP53; BCC7; LFS1; P53; TRP53; p53; TP53; BMFS5
Size: 100 µl
Concentration: See labels on tube
Host Species: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat
Immunogen: A synthetic phosphorylated peptide surrounding S392 of human p53 (NP_000537.3).
Swiss Prot. #: P04637
Calculated MW: 53 kDa
Detected MW: 53 kDa
Applications: WB (1:500 - 1:2,000)
IP (not tested)
IHC (not tested)
IF (not tested)
Note: Antibody dilution should be optimized by users.
Purification: Protein A or G affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Storage: Store at -20℃. Centrifuge to maximize product recovery.
PDF Data Sheet: PDF DatasheetMSDS
Image(s): (Click image to enlarge)


Shipping Method: Wet ice shipping
References: 1. Vogelstein B and Kinzler KW, (1994) Nature 370, 174 - 175.
2. Levine AJ, (1997) Cell 88, 323 - 331.
3. Lu H, et al. (1997) Mol Cell Biol 17(10), 5923 - 5934.

Details

P53 is a tumor suppressor that plays a role in maintaining genomic stability and controlling apoptosis. During the cell cycle, it can arrest cells at the G1/S checkpoint and activate DNA repair mechanisms. It is the most mutated gene in cancer. In unstressed cells, p53 usually exists at low levels in an inactive form, being bound to Mdm2. Phosphorylation of p53 at Ser392 is increased in human tumors and has been reported to influence the growth suppressor function, DNA binding, and transcriptional activation of p53.