MDM2 Recombinant Rabbit Monoclonal Antibody

The MDM2 (murine double minute-2) protein was initially identified as an oncogene in a murine transformation system. MDM2 functions to bind p53 and block p53-mediated transactivation of cotransfected reporter constructs. p53 is the most commonly mutated gene in human cancer identified to date. Expression of p53 leads to inhibition of cell growth by preventing progression of cells from G1 to S phase of the cell cycle. Most importantly, p53 functions to cause arrest of cells in the G1 phase of the cell cycle following any exposure of cells to DNA-damaging agents. The MDM2 gene is amplified in a high percentage of human sarcomas that retain wt p53 and tumor cells that overexpress MDM2 can tolerate high levels of p53 expression. These findings argue that MDM2 overexpression represents at least one mechanism by which p53 function can be abrogated during tumorigenesis.

Specifications

Catalog No.
BX50226
Clone No.
BP6203
Application
IHC-P
Subcellular location
Nucleus
Control
Dedifferentiated liposarcoma
Recommended method
HIER
Volume
100μl/vial, 1ml/vial
Dilution
1:100-1:200
Immunogen
Synthetic peptide within Human MDM2.

Reference

1. Boudreau, C.E., et al. 2017. Vet. Comp. Oncol. 15: 133-150.
2. Lee, E.W., et al. 2017. BMB Rep. 50: 373-378.

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