Anti-PEX16 Antibody Picoband® FITC Conjugated

The protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described

A synthetic peptide corresponding to a sequence at the N-terminus of human PEX16. Human PEX16 shares 94.4% amino acid (aa) sequence identity with mouse PEX16.