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CFC1 encodes a member of the epidermal growth factor (EGF)- Cripto, Frl-1, and Cryptic (CFC) family, which are involved in signalling during embryonic development. Zusätzlich bieten wir Ihnen CFC1 Antikörper (51) und CFC1 Proteine (9) und viele weitere Produktgruppen zu diesem Protein an.
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The knockdown and overexpression of CFC1 were performed using a lentiviral system in NB cell lines. The overexpression of CFC1 increased sphere formation, cell growth, and colony formation.
Results demonstrated that over expression of Snail suppresses Cryptic expression and confirmed that Snail directly binds to Cryptic gene promoter and regulates its expression.
enhances macrophage phagocytic activity and upregulates the production of anti- and pro-inflammatory cytokines via the NF-kappaB signaling pathway
Data indicate that the duplication and deletion of CFC1 protein may play key roles in the occurrence of heterotaxy syndrome.
CFC1 may be involved in the etiology of non-syndromic congenital heart disease in a Chinese population.
CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle
results suggest that heterozygous cryptic family 1 (CFC1) mutation may represent a genetic predisposition to biliary atresia splenic malformation syndrome
Characterization of the glycosylphosphatidylinositol-anchor signal sequence of human Cryptic with a hydrophilic extension is reported.
Functional redundancy of the Cfc1 gene in epiblast and extraembryonic patterning during early mouse embryogenesis is reported.
Cripto, which encodes a Nodal co-receptor, is a primary target of beta-catenin signals in embryogenesis.
cells coexpressing GRP78 and Cripto grow much more rapidly in soft agar than do cells expressing either protein individually
This gene encodes a member of the epidermal growth factor (EGF)- Cripto, Frl-1, and Cryptic (CFC) family, which are involved in signalling during embryonic development. Proteins in this family share a variant EGF-like motif, a conserved cysteine-rich domain, and a C-terminal hydrophobic region. The protein encoded by this gene is necessary for patterning the left-right embryonic axis. Mutations in this gene are associated with defects in organ development, including autosomal visceral heterotaxy and congenital heart disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
cripto, FRL-1, cryptic family 1
, cripto, FRL-1, cryptic family 1B
, cryptic protein
, fibroblast growth factor receptor ligand 1
, cryptic family protein 1
, CRIPTO-related factor 1