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ACOX1 antibody
ACOX1
Reactivity: Human, Mouse, Rat
ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-ACOX1 Antibody
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Target
See all ACOX1 Antibodies
ACOX1
(Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
Reactivity
Human, Mouse, Rat
Host
All hosts for ACOX1 antibodies
Rabbit
Clonality
All clonalities for ACOX1 antibodies
Polyclonal
Conjugate
All conjugates for ACOX1 antibodies
This ACOX1 antibody is un-conjugated
Application
All applications for ACOX1 antibodies
ELISA, Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant protein of human ACOX1
Isotype
IgG
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Discover our top product ACOX1 Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC 1:50-1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.4 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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 Details for ACOX1
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Target
ACOX1
(Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
Alternative Name
ACOX1 (ACOX1 Products )
Synonyms
zgc:92584 antibody, wu:fb59h12 antibody, zgc:114033 antibody, aco antibody, acox antibody, ACOX antibody, PALMCOX antibody, SCOX antibody, RATACOA1 antibody, AOX antibody, Acox antibody, D130055E20Rik antibody, Paox antibody, PCOX1 antibody, acyl-CoA oxidase 1 antibody, acyl-CoA oxidase 1, palmitoyl antibody, acyl-CoA oxidase 1, palmitoyl L homeolog antibody, acyl-Coenzyme A oxidase 1, palmitoyl antibody, ACOX1 antibody, acox1 antibody, acox1.L antibody, Acox1 antibody
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.
UniProt
Q15067
Pathways
Regulation of Lipid Metabolism by PPARalpha , Monocarboxylic Acid Catabolic Process
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