This is a synthetic peptide designed for use in combination with anti-PHYH Antibody(ARP56681_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
Alias Symbols: LN1, LNAP1, PAHX, PHYH1, RD
Protein Interaction Partner: ACSL6,F8,FKBP4,MAGEA11,PEX7,PHYH,PHYHIP,TOM1L1,COPS3,F8,FKBP4,MAGEA11,PEX7,TOM1L1,WDR8