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ACOX1 antibody

This Mouse Monoclonal antibody specifically detects ACOX1 in WB, IF, ICC and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN5541563

Quick Overview for ACOX1 antibody (ABIN5541563)

Target

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

Reactivity

  • 57
  • 21
  • 3
Human

Host

  • 53
  • 5
Mouse

Clonality

  • 47
  • 11
Monoclonal

Conjugate

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

Application

  • 41
  • 34
  • 17
  • 11
  • 8
  • 4
  • 2
  • 2
Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

153CT43-1-1
  • Specificity

    This antibody recognizes Human ACOX1. Other species not tested.

    Purification

    Protein G Chromatography, followed by dialysis against PBS

    Immunogen

    ACOX1 recombinant protein.

    Isotype

    IgG1
  • Application Notes

    Western blot: 1/100-1/500. Immunofluorescence: 1/10-1/50. Immunohistochemistry on Paraffin Sections: 1/10-1/50.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS Preservatives: 0.09 % (W/V) Sodium Azide

    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

    4 °C,-20 °C

    Storage Comment

    Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. Shelf life: one year from despatch.

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    acox1

    Background

    ACOX1 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. Function: Catalyzes the desaturation of acyl-CoAs to 2-trans- enoyl-CoAs. Isoform 1 shows highest activity against medium-chain fatty acyl-CoAs and activity decreases with increasing chain length. Isoform 2 is active against a much broader range of substrates and shows activity towards very long-chain acyl-CoAs. Isoform 2 is twice as active as isoform 1 against 16-hydroxy- palmitoyl-CoA and is 25 % more active against 1,16-hexadecanodioyl- CoA. Cellular Location: Peroxisome. Tissue Location: Widely expressed with highest levels of isoform 1 and isoform 2 detected in testis. Isoform 1 is expressed at higher levels than isoform 2 in liver and kidney while isoform 2 levels are higher in brain, lung, muscle, white adipose tissue and testis. Levels are almost equal in heart.

    UniProt

    Q15067

    Pathways

    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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