JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

PHYH Antibodies

AND PHYH ELISA kits, PHYH Proteins

Many biological assays use antibodies to detect PHYH, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with PHYH in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop PHYH antibodies...

We validate the specificity of these antibodies to PHYH by testing them on tissues known to express PHYH positively and negatively. Browse below to find the PHYH antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

Previous: CBLIF Next: SERPINB6

PHYH Infographic by Boster Bio

PHYH protein infographic

All PHYH Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-PHYH Antibody

Human, Mouse

WB

$405
Cat # A05846
100ul

PHYH (NM_006214) Human Over-expression Lysate

Human

$628
Cat # LS005264
100 µg

PHYH Overview

Facts about Phytanoyl-CoA dioxygenase, peroxisomal.

PHYH 3D structure

PHYH 3D structure. Source: alphafold

Phytanoyl-CoA dioxygenase, peroxisomal (PHYH)

Converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. .

Gene Information

Human
Gene Name:	PHYH
Uniprot:	O14832
Entrez:	5264

Gene Information

Family

Belongs to:

PhyH family

Family

Alternative Names

LNAP1; PAHXLN1; peroxisomal; PhyH; PHYH1; phytanoyl-CoA 2-hydroxylase; phytanoyl-CoA hydroxylase (Refsum disease); phytanoyl-CoA hydroxylase; RD

Molecular Weight

Mass (kDA):
38.538 kDA

Molecular Weight

Genomic Context


Human

Location:	10p13
Sequence:	10; NC_000010.11 (13277796..13300130, complement)

Tissue Specificity

Expressed in liver, kidney, and T-cells, but not in spleen, brain, heart, lung and skeletal muscle.

Subcellular Localizations

Peroxisome.

Subcellular Localization

Diseases

Refsum Disease
Retinitis Pigmentosa
Ataxia
Polyneuropathy
Peroxisomal Disorders
Cerebellar Ataxia
Anosmia
Sensory Neuropathy
Chondrodysplasia Punctata
Chondrodysplasia Punctata, Rhizomelic
Blind Vision

Peripheral Neuropathy
Nervousness
Complete Hearing Loss
Nervous System Disorder
Acidemia
Neoplasms

Disease

Interacting Proteins

FAM9B
MAGEA11

Interacting Proteins

Pathways

Localization
Transport
Cell Differentiation
Pathogenesis
Fatty Acid Oxidation
Ras Protein Signal Transduction
Cell Adhesion
Neurogenesis
Positive Regulation Of Fat Cell Differentiation
System Development
Fatty Acid Transport
Cell Cycle
Regulation Of Mitosis

Regulation Of Fat Cell Differentiation
Lipid Storage
Lipid Transport
Visual Perception
Cell Proliferation
Circadian Rhythm
Establishment Of Blood-nerve Barrier

Pathways

PTMs

Oxidation
Hydroxylation

Phosphorylation
Cleavage

Research Areas

Lipid and Metabolism
Vision

Research Areas

Bosterbio | ELISA Kits, Antibodies, Antibody Company

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/PHYH

References

PMID: 9326939 by Mihalik S.J., et al. Identification of PAHX, a Refsum disease gene.

PMID: 9326940 by Jansen G.A., et al. Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene.