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PHYH antibody

PHYH Reactivity: Human, Mouse IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6570342
  • Target See all PHYH Antibodies
    PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
    Reactivity
    • 55
    • 13
    • 5
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Mouse
    Host
    • 49
    • 7
    Rabbit
    Clonality
    • 50
    • 5
    Polyclonal
    Conjugate
    • 25
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This PHYH antibody is un-conjugated
    Application
    • 48
    • 25
    • 19
    • 13
    • 13
    • 13
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human PHYH (NP_006205.1).
    Isotype
    IgG
    Top Product
    Discover our top product PHYH Primary Antibody
  • Application Notes
    IF 1:10-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
    Alternative Name
    PHYH (PHYH Products)
    Synonyms
    zgc:110203 antibody, LN1 antibody, LNAP1 antibody, PAHX antibody, PHYH1 antibody, RD antibody, AI256161 antibody, AI265699 antibody, Lnap1 antibody, phytanoyl-CoA 2-hydroxylase antibody, phytanoyl-CoA hydroxylase-like antibody, phytanoyl-CoA hydroxylase antibody, PHYH antibody, LOC478001 antibody, phyh antibody, Phyh 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.
    Molecular Weight

    Observed_MW: 40kDa

    Calculated_MW: 27kDa/38kDa

    Gene ID
    5264
    UniProt
    O14832
    Pathways
    Monocarboxylic Acid Catabolic Process
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