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Anti-Human/Mouse PHYH Polyclonal Antibody

Categories: [ Antibodies][ Polyclonal Antibodies]
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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Properties

Data Sheet Click for Datasheet
Catalog Number PA11817
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human PHYH
Specificity Expressed in liver, kidney, and T-cells, but not in spleen, brain, heart, lung and skeletal muscle.
Isotype IgG
Reacitivity Human,Mouse
Clone
Uniprot O14832
Concentration 0.2 mg/mL
Dilution WB 1:500-1:2000, IHC 1:25-1:100
Formulation
Application WB,IHC,ELISA
Other Names 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
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.
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