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RNF11 Antibody (Center) Blocking peptide

Synthetic peptide

     
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Product Information
Primary Accession Q9Y3C5
Clone Names 90504146
Additional Information
Gene ID 26994
Other Names RING finger protein 11, RNF11
Format Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name RNF11
Function Essential component of a ubiquitin-editing protein complex, comprising also TNFAIP3, ITCH and TAX1BP1, that ensures the transient nature of inflammatory signaling pathways. Promotes the association of TNFAIP3 to RIPK1 after TNF stimulation. TNFAIP3 deubiquitinates 'Lys- 63' polyubiquitin chains on RIPK1 and catalyzes the formation of 'Lys- 48'-polyubiquitin chains. This leads to RIPK1 proteasomal degradation and consequently termination of the TNF- or LPS-mediated activation of NF-kappa-B. Recruits STAMBP to the E3 ubiquitin-ligase SMURF2 for ubiquitination, leading to its degradation by the 26S proteasome.
Cellular Location Early endosome. Recycling endosome. Cytoplasm. Nucleus. Note=Predominantly cytoplasmic, when unphosphorylated, and nuclear, when phosphorylated by PKB/AKT1
Tissue Location Expressed at low levels in the lung, liver, kidney, pancreas, spleen, prostate, thymus, ovary, small intestine, colon, and peripheral blood lymphocytes, and, at intermediate levels, in the testis, heart, brain and placenta. Highest expression in the skeletal muscle. In the brain, expressed at different levels in several regions: high levels in the amygdala, moderate in the hippocampus and thalamus, low in the caudate and extremely low levels in the corpus callosum (at protein level). Restricted to neurons, enriched in somatodendritic compartments and excluded from white matter (at protein level). In substantia nigra, present in cell bodies and processes of dopaminergic and nondopaminergic cells (at protein level). In Parkinson disease, sequestered in Lewy bodies and neurites. Overexpressed in breast cancer cells, but not detected in the surrounding stroma and weakly, if at all, in normal breast epithelial cells (at protein level). Also expressed in several tumor cell lines.
Research Areas
Citations (0)
citation

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Background

The protein encoded by this gene contains a RING-H2 fingermotif, which is known to be important for protein-proteininteractions. The expression of this gene has been shown to beinduced by mutant RET proteins (MEN2A/MEN2B). The germlinemutations in RET gene are known to be responsible for thedevelopment of multiple endocrine neoplasia (MEN). [provided byRefSeq].

References

Santonico, E., et al. Oncogene 29(41):5604-5618(2010)Markson, G., et al. Genome Res. 19(10):1905-1911(2009)Shembade, N., et al. EMBO J. 28(5):513-522(2009)van Wijk, S.J., et al. Mol. Syst. Biol. 5, 295 (2009) :Chen, C., et al. Oncogene 27(54):6845-6855(2008)

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$ 277.78
Cat# BP12908c
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