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RCBTB1 encodes a protein with an N-terminal RCC1 domain and a C-terminal BTB (broad complex, tramtrack and bric-a-brac) domain. De plus, nous expédions RCBTB1 Anticorps (76) et RCBTB1 Protéines (5) et beaucoup plus de produits pour cette protéine.
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study puts forward mutations in RCBTB1 as a cause of autosomal-recessive non-syndromic and syndromic inherited retinal dystrophies; data support a role for impaired ubiquitination in the pathogenetic mechanism of RCBTB1 mutations
Results identified RCBTB1 as a gene associated with vitreoretinopathy and found that it plays a role in retinal angiogenesis through Norrin (Montrer NDP Kits ELISA)-induced beta-catenin (Montrer CTNNB1 Kits ELISA) signaling.
Study identifies RCBTB1 as a modifier of the smoking effect on carotid intima-media thickness.
Data show that the biological actions of Clld7 are consistent with those of a tumor suppressor.
This gene encodes a protein with an N-terminal RCC1 domain and a C-terminal BTB (broad complex, tramtrack and bric-a-brac) domain. In rat, over-expression of this gene in vascular smooth muscle cells induced cellular hypertrophy. In rat, the C-terminus of RCBTB1 interacts with the angiotensin II receptor-1A. In humans, this gene maps to a region of chromosome 13q that is frequently deleted in B-cell chronic lymphocytic leukemia and other lymphoid malignancies.
RCC1 and BTB domain-containing protein 1
, regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1
, RCC1 and BTB domain-containing protein 1-like
, CLL deletion region gene 7 protein
, GDP/GTP exchange factor (GEF)-like protein
, chronic lymphocytic leukemia deletion region gene 7 protein
, regulator of chromosome condensation and BTB domain-containing protein 1