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Phenylalanine Hydroxylase antibody

Reactivity: Human, Mouse, Rat WB, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7009050
  • Target See all Phenylalanine Hydroxylase Antibodies
    Phenylalanine Hydroxylase
    Reactivity
    Human, Mouse, Rat
    Host
    • 44
    • 7
    • 1
    Rabbit
    Clonality
    • 47
    • 5
    Polyclonal
    Conjugate
    • 25
    • 8
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Phenylalanine Hydroxylase antibody is un-conjugated
    Application
    • 40
    • 24
    • 14
    • 6
    • 5
    • 4
    • 4
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human PAH (NP_000268.1).
    Isotype
    IgG
    Top Product
    Discover our top product Phenylalanine Hydroxylase Primary Antibody
  • Application Notes
    WB 1:500-1:2000 IF 1:50-1:200
    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
    Phenylalanine Hydroxylase
    Alternative Name
    PAH (Phenylalanine Hydroxylase Products)
    Synonyms
    cb877 antibody, wu:fb02f10 antibody, zgc:65981 antibody, GB18494 antibody, PAH antibody, pku antibody, pku1 antibody, DDBDRAFT_0206188 antibody, DDBDRAFT_0231664 antibody, DDB_0206188 antibody, DDB_0231664 antibody, AW106920 antibody, PH antibody, PKU antibody, PKU1 antibody, phenylalanine-4-hydroxylase antibody, phenylalanine hydroxylase antibody, protein henna antibody, phenylalanine 4-monooxygenase antibody, pah antibody, LOC408622 antibody, PAH antibody, CpipJ_CPIJ002149 antibody, Pah antibody
    Background
    PAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.
    Molecular Weight

    Observed_MW: 55 kDa

    Calculated_MW: 51 kDa

    Gene ID
    5053
    UniProt
    P00439
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