Product Type: Antibody
Descritpion: 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 Areas: Cancer, Metabolism, Neuroscience, Signal transduction
Recommended Dilutions: IHC 1:25-1:100
Size: 200 uL
Gene Accession: BC029512
Immunogen: Recombinant protein of human PHYH
Formulation: PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Purification: Affinity purification
Tissue Specificity/Positive Control: Expressed in liver, kidney, and T-cells, but not in spleen, brain, heart, lung and skeletal muscle.
Cellular Localization: Peroxisome.
Storage: Store at -20C. Avoid freeze / thaw cycles.
Product Link: https://www.elabscience.com/p-phyh_polyclonal_antibody-31526.html
Manual Link: https://www.elabscience.com/viewpdf-31526-elabscience-E-AB-11486.PDF