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ACOX1 antibody

The Rabbit Polyclonal anti-ACOX1 antibody has been validated for WB. It is suitable to detect ACOX1 in samples from Human.
Catalog No. ABIN7469233

Quick Overview for ACOX1 antibody (ABIN7469233)

Target

See all ACOX1 Antibodies
ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))

Reactivity

  • 57
  • 21
  • 3
Human

Host

  • 52
  • 6
Rabbit

Clonality

  • 46
  • 12
Polyclonal

Conjugate

  • 32
  • 5
  • 5
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ACOX1 antibody is un-conjugated

Application

  • 41
  • 34
  • 17
  • 12
  • 9
  • 4
  • 3
  • 2
Western Blotting (WB)
  • Cross-Reactivity

    Human

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human ACOX1. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: HepG2

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.89 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))

    Alternative Name

    ACOX1

    Background

    Synonyms: acyl-CoA oxidase 1 , ACOX , PALMCOX , SCOX

    Background: The protein encoded by this gene is the first enzyme of the fatty acid beta-oxidation pathway, which catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq]

    Molecular Weight

    74 kDa

    Gene ID

    51

    UniProt

    Q15067

    Pathways

    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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