Product Pathways - Akt Signaling
PTEN (D4.3) Rabbit mAb #9188
| Applications | Reactivity | Sensitivity | MW (kDa) | Isotype |
|---|---|---|---|---|
| W IP IHC-P IF-IC F | H M R Mk | Endogenous | 55 | Rabbit IgG |
Applications Key:
W=Western Blotting
IP=Immunoprecipitation
IHC-P=Immunohistochemistry (Paraffin)
IF-IC=Immunofluorescence (Immunocytochemistry)
F=Flow Cytometry
Reactivity Key:
H=Human
M=Mouse
R=Rat
Mk=Monkey
Species cross-reactivity is determined by Western blot.
Specificity / Sensitivity
PTEN (D4.3) Rabbit mAb detects endogenous levels of total PTEN protein.
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide (KLH-coupled) corresponding to residues in the carboxy-terminal sequence of human PTEN.
Western Blotting
Western blot analysis of extracts from various cell lines using PTEN (D4.3) Rabbit mAb (upper) and Akt (pan) (C67E7) Rabbit mAb #4691 (lower).
IHC-P (paraffin)
Immunohistochemical analysis of paraffin-embedded human colon using PTEN (D4.3) Rabbit mAb.
IHC-P (paraffin)
Immunohistochemical analysis of SignalSlide(TM) PTEN IHC Controls #8106 (LNCaP) (left) and NIH/3T3 (right) paraffin-embedded cell pellets) using PTEN (D4.3) Rabbit mAb.
Background
PTEN (phosphatase and tensin homologue deleted on chromosome ten), also referred to as MMAC (mutated in multiple advanced cancers) phosphatase, is a tumor suppressor implicated in a wide variety of human cancers (1). PTEN encodes a 403 amino acid polypeptide originally described as a dual-specificity protein phosphatase (2). The main substrates of PTEN are inositol phospholipids generated by the activation of the phosphoinositide 3-kinase (PI3K) (3). PTEN is a major negative regulator of the PI3K/Akt signaling pathway (1,4,5). PTEN possesses a carboxy-terminal, noncatalytic regulatory domain with three phosphorylation sites (Ser380, Thr382 and Thr383) that regulate PTEN stability and may affect its biological activity (6,7). PTEN regulates p53 protein levels and activity (8) and is involved in G protein coupled signaling during chemotaxis (9,10).
- Cantley, L.C. and Neel, B.G. (1999) Proc. Natl. Acad. Sci. U S A 96, 4240-4245.
- Myers, M.P. et al. (1997) Proc. Natl. Acad. Sci. U S A 94, 9052-9057.
- Myers, M.P. et al. (1998) Proc. Natl. Acad. Sci U S A 95, 13513-13518.
- Wan, X. and Helman, L.J. (2003) Oncogene 22, 8205-8211.
- Wu, X. et al. (1998) Proc. Natl. Acad. Sci. U S A 95, 15587-15591.
- Vazquez, F. et al. (2000) Mol. Cell. Biol. 20, 5010-5018.
- Torres, J. and Pulido, R. (2001) J. Biol. Chem. 276, 993-998.
- Freeman, D.J. et al. (2003) Cancer Cell 3, 117-130.
- Funamoto, S. et al. (2002) Cell 109, 611-623.
- Iijima, M. and Devreotes, P. (2002) Cell 109, 599-610.
Application References
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- 9998 BSA
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This product is for in vitro research use only and is not intended for use in humans or animals. This product is not intended for use as therapeutic or in diagnostic procedures.