Product Pathways - PI3K / Akt Signaling
YAP/TAZ (D24E4) Rabbit mAb #8418
|8418S||100 µl (10 western blots)||---||In Stock||---|
|8418||carrier free and custom formulation / quantity||email request|
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|W||1:1000||Human, Mouse, Monkey||Endogenous||50, 70||Rabbit IgG|
Species cross-reactivity is determined by western blot.
Applications Key: W=Western Blotting, IP=Immunoprecipitation, IHC-P=Immunohistochemistry (Paraffin)
Specificity / Sensitivity
YAP/TAZ (D24E4) Rabbit mAb recognizes endogenous levels of total YAP and TAZ proteins.
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Asp362 of human TAZ protein.
Western blot analysis of extracts from various cell lines using YAP/TAZ (D24E4) Rabbit mAb.
Immunohistochemical analysis of paraffin-embedded human colon carcinoma using YAP/TAZ (D24E4) Rabbit mAb.
Immunohistochemical analysis of paraffin-embedded human lymphoma using YAP/TAZ (D24E4) Rabbit mAb.
YAP (Yes-associated protein, YAP65) was identified based on its ability to associate with the SH3 domain of Yes. It also binds to other SH3 domain-containing proteins such as Nck, Crk, Src, and Abl (1). In addition to the SH3 binding motif, YAP contains a PDZ interaction motif, a coiled-coil domain, and WW domains (2-4). While initial studies of YAP all pointed towards a role in anchoring and targeting to specific subcellular compartments, subsequent studies showed that YAP is a transcriptional co-activator by virtue of its WW domain interacting with the PY motif (PPxY) of the transcription factor PEBP2 and other transcription factors (5,6). Upon phosphorylation at Ser127, YAP interacts with 14-3-3 in an Akt-dependent manner and suppresses p73-mediated apoptosis (6).
YAP may also function as a transcriptional repressor (7) and is now recognized as a critical regulator of the Hippo (Mst1/Mst2) signaling pathway (8). YAP may therefore play an important role in both organ size determination and tumor suppression (8).
TAZ is a closely related transcriptional co-activator also implicated in the Hippo signaling pathway (9). Taz contains a PDZ-binding motif, which shares homology with the WW domain of YAP, and has been proposed to modulate the switch between proliferation and differentiation of mesenchymal stem cells (MSCs) via interaction with the transcription factors Runx2 and PPARγ. This process is critical for normal tissue development and tumor suppression (10). Due to its role in the determination of MSC fate, TAZ may have clinical relevance to several human diseases caused by an imbalance of MSC differentiation (11).
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- Mohler, P. et al. (1999) J. Cell Biol. 147, 879-890.
- Espanel, X. and Sudol, M. (2001) J. Biol. Chem. 276, 14514-14523.
- Sudol, M. et al. (1995) FEBS Lett. 369, 67-71.
- Yagi, R. et al. (1999) EMBO J. 18, 2551-2562.
- Basu, S. et al. (2003) Mol. Cell 11, 11-23.
- Zaidi, S.K. et al. (2004) EMBO J 23, 790-9.
- Pan, D. (2010) Dev Cell 19, 491-505.
- Kanai, F. et al. (2000) EMBO J 19, 6778-91.
- Hong, J.H. et al. (2005) Science 309, 1074-8.
- Hong, J.H. and Yaffe, M.B. (2006) Cell Cycle 5, 176-9.
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For Research Use Only. Not For Use In Diagnostic Procedures.
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