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CCDC50 encodes a soluble, cytoplasmic, tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains. Zusätzlich bieten wir Ihnen Coiled-Coil Domain Containing 50 Kits (12) und Coiled-Coil Domain Containing 50 Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 82 products:
Human Polyclonal CCDC50 Primary Antibody für ICC, IF - ABIN4366523
Farfsing, Engel, Seiffert, Hartmann, Ott, Rosenwald, Stilgenbauer, Döhner, Boutros, Lichter, Pscherer: Gene knockdown studies revealed CCDC50 as a candidate gene in mantle cell lymphoma and chronic lymphocytic leukemia. in Leukemia 2009
Human Polyclonal CCDC50 Primary Antibody für IHC (p), IHC - ABIN250431
Blagoev, Ong, Kratchmarova, Mann: Temporal analysis of phosphotyrosine-dependent signaling networks by quantitative proteomics. in Nature biotechnology 2004
Up to now, merely 7 loci have been linked to mid-frequency hearing loss. Only four genetic mid-frequency deafness genes, namely, DFNA10 (EYA4 (zeige EYA4 Antikörper)), DFNA8 (zeige TECTA Antikörper)/12 (TECTA (zeige TECTA Antikörper)), DFNA13 (COL11A2 (zeige COL11A2 Antikörper)), DFNA44 (CCDC50), have been reported to date. [review]
Ymer acts as a regulator downstream of several receptors and that Ymer functions as a positive or negative regulator in a signaling pathway-dependent manner.
identification of a novel DFNA locus on chromosome 3q28-29 in a Spanish family with postlingual and progressive hearing loss[DFNA44]
Ymer functions as a novel inhibitor for the down-regulation of the EGF receptor (zeige EGFR Antikörper) and plays a crucial role for regulating the amount of the EGF receptor (zeige EGFR Antikörper) on the cell surface membrane
These findings demonstrate that Ymer is likely to be a negative regulator for the NF-kappaB (zeige NFKB1 Antikörper) signaling pathway.
CCDC50 is required for survival in mantle cell lymphoma and chronic lymphocytic leukemia cells and controls NFkappaB signaling
This gene encodes a soluble, cytoplasmic, tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains. Mutations in this gene cause nonsyndromic, postlingual, progressive sensorineural DFNA44 hearing loss. In mouse, the protein is expressed in the inner ear during development and postnatal maturation and associates with microtubule-based structures. This protein may also function as a negative regulator of NF-kB signaling and as an effector of epidermal growth factor (EGF)-mediated cell signaling. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
coiled-coil domain containing 50
, Ymer protein
, coiled-coil domain-containing protein 50
, protein Ymer
, putative C3orf6 protein homolog