ACOX1 anticorps (C-Term)

N° du produit ABIN5535442

Détail du produit anti-ACOX1 anticorps

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

Épitope: AA 629-659, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACOX1 est non-conjugé

Application: Western Blotting (WB)

Purification: This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis

Immunogène: This ACOX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 629-659 amino acids from the C-terminal region of human ACOX1.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 2 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur ACOX1

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

Autre désignation: ACOX1 (ACOX1 Produits)

Synonymes: anticorps zgc:92584, anticorps wu:fb59h12, anticorps zgc:114033, anticorps aco, anticorps acox, anticorps ACOX, anticorps PALMCOX, anticorps SCOX, anticorps RATACOA1, anticorps AOX, anticorps Acox, anticorps D130055E20Rik, anticorps Paox, anticorps PCOX1, anticorps acyl-CoA oxidase 1, anticorps acyl-CoA oxidase 1, palmitoyl, anticorps acyl-CoA oxidase 1, palmitoyl L homeolog, anticorps acyl-Coenzyme A oxidase 1, palmitoyl, anticorps ACOX1, anticorps acox1, anticorps acox1.L, anticorps Acox1

Sujet: 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.

Poids moléculaire: 74 kDa

ID gène: 51

UniProt: Q15067

Pathways: Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process