CFC1 Rabbit Polyclonal Antibody, 50ul Nucleic Acid Extraction including the heart

including the heart

A mutation in PEX14 results in one form of Zellweger syndrome

Chromosome 8 is also associated with Pfeiffer syndrome

The encoded protein binds calcium and is activated by myosin light chain kinase

a coiled-coil motif and a C-terminal Rab domain

CFC1 Rabbit Polyclonal Antibody, 50ul Nucleic Acid Extraction including the heartThis 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