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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. Additionally we are shipping CFC1 Antibodies (34) and CFC1 Proteins (8) and many more products for this protein.
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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
Functional redundancy of the Cfc1 gene in epiblast and extraembryonic patterning during early mouse embryogenesis is reported.
Cripto (show TDGF1 ELISA Kits), which encodes a Nodal co-receptor, is a primary target of beta-catenin (show CTNNB1 ELISA Kits) signals in embryogenesis.
cells coexpressing GRP78 (show HSPA5 ELISA Kits) and Cripto (show TDGF1 ELISA Kits) 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