PHYH Polyclonal Antibody

Rs. 16,500.00
SKU E-AB-15297


Synonyms LN1,LNAP1,LNAP1,mouse,homolog of,OTTHUMP00000019131,OTTHUMP00000019132,OTTHUMP00000179083,OTTHUMP00000216226,PAHX,PAHX,peroxisomal,PhyH,PHYH1,Phytanic acid oxidase,phytanoil-CoA alpha hydroxylase,phytanoyl CoA 2 hydroxylase,Phytanoyl CoA 2 oxoglutarate dioxygenase,Phytanoyl CoA alpha hydroxylase,Phytanoyl CoA dioxygenase,Phytanoyl CoA dioxygenase peroxisomal,Phytanoyl-CoA alpha-hydroxylase,Phytanoyl-CoA dioxygenase,RD
Swissprot O14832
Source Rabbit
Reactivity Human,Mouse
Immunogen Recombinant protein of human PHYH
Application WB,IHC,ELISA
Recommended dilution WB 1:500-1:2000, IHC 1:25-1:100
Concentration 0.2mg/mL
Clonality Polyclonal


Cellular localization  
Tissue specificity  
Isotype IgG
Purification Affinity purification
Conjugation Unconjugated
Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
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.


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