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Phenylalanine Hydroxylase anticorps (AA 71-208)

Reactivité: Humain WB, IHC (p) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5518942
  • Antigène Voir toutes Phenylalanine Hydroxylase Anticorps
    Phenylalanine Hydroxylase
    Épitope
    • 7
    • 7
    • 6
    • 6
    • 6
    • 4
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 71-208
    Reactivité
    • 52
    • 22
    • 15
    Humain
    Hôte
    • 45
    • 7
    • 1
    Lapin
    Clonalité
    • 48
    • 5
    Polyclonal
    Conjugué
    • 26
    • 8
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Phenylalanine Hydroxylase est non-conjugé
    Application
    • 41
    • 25
    • 15
    • 5
    • 5
    • 5
    • 4
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Fonction
    Rabbit IgG polyclonal antibody for Phenylalanine-4-hydroxylase(PAH) detection. Tested with WB, IHC-P in Human,Mouse,Rat.
    Réactivité croisée (Details)
    No cross reactivity with other proteins.
    Attributs du produit
    Rabbit IgG polyclonal antibody for Phenylalanine-4-hydroxylase(PAH) detection. Tested with WB, IHC-P in Human,Mouse,Rat.
    Gene Name: phenylalanine hydroxylase
    Protein Name: Phenylalanine-4-hydroxylase
    Purification
    Immunogen affinity purified.
    Immunogène
    E. coli-derived human PAH recombinant protein (Position: R71-H208). Human PAH shares 89.1% and 88.4% amino acid (aa) sequence identity with mouse and rat PAH, respectively.
    Isotype
    IgG
    Top Product
    Discover our top product Phenylalanine Hydroxylase Anticorps primaire
  • Indications d'application
    WB: Concentration: 0.1-0.5 μg/mL, Tested Species: Human, Mouse, Rat
    IHC-P: Concentration: 0.5-1 μg/mL, Tested Species: Human, Mouse, Rat, Epitope Retrieval by Heat: Boiling the paraffin sections in 10 mM citrate buffer, pH 6.0, for 20 mins is required for the staining of formalin/paraffin sections.
    Notes: Tested Species: Species with positive results. Other applications have not been tested. Optimal dilutions should be determined by end users.
    Commentaires

    Boster recommends Enhanced Chemiluminescent Kit with anti-Rabbit IgG (ABIN921124) for Western blot, and HRP Conjugated anti-Rabbit IgG Super Vision Assay Kit (SV0002-1) for IHC(P).

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
    Concentration
    500 μg/mL
    Buffer
    Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Sodium azide.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    At -20°C for one year. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20 °C for a longer time. Avoid repeated freezing and thawing.
  • Antigène
    Phenylalanine Hydroxylase
    Autre désignation
    PAH (Phenylalanine Hydroxylase Produits)
    Synonymes
    anticorps cb877, anticorps wu:fb02f10, anticorps zgc:65981, anticorps GB18494, anticorps PAH, anticorps pku, anticorps pku1, anticorps DDBDRAFT_0206188, anticorps DDBDRAFT_0231664, anticorps DDB_0206188, anticorps DDB_0231664, anticorps AW106920, anticorps PH, anticorps PKU, anticorps PKU1, anticorps phenylalanine-4-hydroxylase, anticorps phenylalanine hydroxylase, anticorps protein henna, anticorps phenylalanine 4-monooxygenase, anticorps pah, anticorps LOC408622, anticorps PAH, anticorps CpipJ_CPIJ002149, anticorps Pah
    Classe de substances
    Chemical
    Sujet
    Phenylalanine hydroxylase (PAH) is an enzyme that catalyzes the hydroxylation of the aromatic side-chain of phenylalanine to generate tyrosine. It is one of three members of the biopterin-dependent aromatic amino acid hydroxylases, a class of monooxygenase that uses tetrahydrobiopterin (BH4, a pteridine cofactor) and a non-heme iron for catalysis. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.

    Synonyms: Phenylalanine-4-hydroxylase, PAH, Phe-4-monooxygenase
    ID gène
    5053
    UniProt
    P00439
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