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Acox2 anticorps

Acox2 Reactivité: Humain, Souris IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7256364
  • Antigène Voir toutes Acox2 Anticorps
    Acox2 (Acyl-CoA Oxidase 2, Branched Chain (Acox2))
    Reactivité
    • 34
    • 25
    • 17
    Humain, Souris
    Hôte
    • 44
    • 4
    • 1
    Lapin
    Clonalité
    • 47
    • 2
    Polyclonal
    Conjugué
    • 18
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Acox2 est non-conjugé
    Application
    • 26
    • 23
    • 13
    • 13
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human ACOX2 (NP_003491.1).
    Isotype
    IgG
    Top Product
    Discover our top product Acox2 Anticorps primaire
  • Indications d'application
    IHC 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
    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
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    Acox2 (Acyl-CoA Oxidase 2, Branched Chain (Acox2))
    Autre désignation
    ACOX2 (Acox2 Produits)
    Synonymes
    anticorps BCOX, anticorps BRCACOX, anticorps BRCOX, anticorps THCCox, anticorps THCA, anticorps acyl-CoA oxidase 2, anticorps acyl-CoA oxidase 2, branched chain L homeolog, anticorps acyl-CoA oxidase 2, branched chain, anticorps acyl-Coenzyme A oxidase 2, branched chain, anticorps ACOX2, anticorps acox2.L, anticorps acox2, anticorps Acox2
    Sujet
    The product of this gene belongs to the acyl-CoA oxidase family. It encodes the branched-chain acyl-CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates, and may lead to Zellweger syndrome, severe mental retardation, and death in children.
    ID gène
    8309
    UniProt
    Q99424
    Pathways
    Monocarboxylic Acid Catabolic Process
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