Product Pathways - TGF-beta/Smad Signaling
Smad6 Antibody #9519
PhosphoSitePlus® protein, site, and accession data: Smad6
| Applications | Reactivity | Sensitivity | MW (kDa) | Source |
|---|---|---|---|---|
| W | H Mk | Endogenous | 62 | Rabbit |
Applications Key:
W=Western Blotting
Reactivity Key:
H=Human
Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.
Protocols
- 9519:
- Western Blotting
Specificity / Sensitivity
Smad6 Antibody detects endogenous levels of total Smad6 protein.
Source / Purification
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding cysteine 55 of human Smad6. Antibodies were purified by protein A and peptide affinity chromatography.
Background
Members of the Smad family of signal transduction molecules are components of a critical intracellular pathway that transmit TGF-β signals from the cell surface into the nucleus. Three distinct classes of Smads have been defined: the receptor-regulated Smads (R-Smads), which include Smad1, 2, 3, 5, and 8; the common-mediator Smad (co-Smad), Smad4; and the antagonistic or inhibitory Smads (I-Smads), Smad6 and 7 (1-5). Activated type I receptors associate with specific R-Smads and phosphorylate them on a conserved carboxy-terminal SSXS motif. The phosphorylated R-Smad dissociates from the receptor and forms a heteromeric complex with the co-Smad (Smad4), allowing translocation of the complex to the nucleus. Once in the nucleus, Smads can target a variety of DNA binding proteins to regulate transcriptional responses (6-8).
The inhibitory Smads, Smad6 and Smad7, were originally identified in vascular endothelium and inhibit TGF-β and BMP signaling by interfering with the phosphorylation of other Smad family members (9,10). Their expression may be induced by TGF-β, and BMP in some cell types providing a negative feedback loop (11,12).
- Heldin, C.H. et al. (1997) Nature 390, 465-471.
- Attisano, L. and Wrana, J.L. (1998) Curr. Opin. Cell Biol. 10, 188-194.
- Derynck, R. et al. (1998) Cell 95, 737-740.
- Massague, J. (1998) Annu. Rev. Biochem. 67, 753-791.
- Whitman, M. (1998) Genes Dev. 12, 2445-2462.
- Wu, G. et al. (2000) Science 287, 92-97.
- Attisano, L. and Wrana, J.L. (2002) Science 296, 1646-1647.
- Moustakas, A. et al. (2001) J. Cell Sci. 114, 4359-4369.
- Topper, J.N. et al. (1997) Proc. Natl. Acad. Sci. USA 94, 9314-9319.
- Imamura, T. et al. (1997) Nature 389, 622-626.
- Takase, M. et al. (1998) Biochem. Biophys. Res. Commun. 244, 26-29.
- Afrakhte, M. et al. (1998) Biochem. Biophys. Res. Commun. 249, 505-511.
Application References
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This product is intended for research purposes only. The product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.