PHYH Polyclonal Antibody

Background:
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.

Research Area: Cancer, Metabolism, Neuroscience, Signal Transduction

Synonyms:
PHYH, LN1, LNAP1, PAHX, PHYH1, RD

Immunogen: Recombinant fusion protein of human PHYH (NP_006205.1).

Swissprot: O14832
Gene ID: 5264

Purification Method: Affinity purification

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Concentration: 1 mg/mL
Dilution: "IF 1:10-1:100"

Storage:
Store at -20°C. Avoid freeze / thaw cycles.