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Acox2 antibody (N-Term)

The Rabbit Polyclonal anti-Acox2 antibody has been validated for WB and EIA. It is suitable to detect Acox2 in samples from Human.
Catalog No. ABIN950243

Quick Overview for Acox2 antibody (N-Term) (ABIN950243)

Target

See all Acox2 Antibodies
Acox2 (Acyl-CoA Oxidase 2, Branched Chain (Acox2))

Reactivity

  • 29
  • 27
  • 18
Human

Host

  • 41
  • 4
  • 1
Rabbit

Clonality

  • 44
  • 2
Polyclonal

Conjugate

  • 20
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Acox2 antibody is un-conjugated

Application

  • 22
  • 18
  • 13
  • 13
  • 6
  • 3
  • 3
  • 3
  • 3
  • 2
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 15
    • 8
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-30, N-Term

    Specificity

    This antibody reacts to ACOX2.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human.

    Purification

    Affinity chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human ACOX2

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) sodium azide as preservative

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    Acox2 (Acyl-CoA Oxidase 2, Branched Chain (Acox2))

    Alternative Name

    ACOX2

    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.Synonyms: 12-alpha-trihydroxy-5-beta-cholestanoyl-CoA 24-hydroxylase, 12-alpha-trihydroxy-5-beta-cholestanoyl-CoA oxidase, 3-alpha, 7-alpha, ACOX-2, EC=1.17.99.3, Peroxisomal acyl-coenzyme A oxidase 2, THCA-CoA oxidase, THCCox, Trihydroxycoprostanoyl-CoA oxidase

    Gene ID

    8309

    NCBI Accession

    NP_003491

    Pathways

    Monocarboxylic Acid Catabolic Process
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