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Acox2 antibody

Acox2 Reactivity: Human, Mouse IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7256364
  • Target See all Acox2 Antibodies
    Acox2 (Acyl-CoA Oxidase 2, Branched Chain (Acox2))
    Reactivity
    • 34
    • 25
    • 17
    Human, Mouse
    Host
    • 44
    • 4
    • 1
    Rabbit
    Clonality
    • 47
    • 2
    Polyclonal
    Conjugate
    • 18
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Acox2 antibody is un-conjugated
    Application
    • 26
    • 23
    • 13
    • 13
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human ACOX2 (NP_003491.1).
    Isotype
    IgG
    Top Product
    Discover our top product Acox2 Primary Antibody
  • Application Notes
    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
    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
    Acox2 (Acyl-CoA Oxidase 2, Branched Chain (Acox2))
    Alternative Name
    ACOX2 (Acox2 Products)
    Synonyms
    BCOX antibody, BRCACOX antibody, BRCOX antibody, THCCox antibody, THCA antibody, acyl-CoA oxidase 2 antibody, acyl-CoA oxidase 2, branched chain L homeolog antibody, acyl-CoA oxidase 2, branched chain antibody, acyl-Coenzyme A oxidase 2, branched chain antibody, ACOX2 antibody, acox2.L antibody, acox2 antibody, Acox2 antibody
    Background
    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.
    Gene ID
    8309
    UniProt
    Q99424
    Pathways
    Monocarboxylic Acid Catabolic Process
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