Acox2 Antikörper (N-Term)

Produktnummer ABIN950243

Produktdetails anti-Acox2 Antikörper

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

Bindungsspezifität: AA 1-30, N-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Acox2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Enzyme Immunoassay (EIA)

Spezifität: This antibody reacts to ACOX2.

Kreuzreaktivität (Details): Species reactivity (tested):Human.

Aufreinigung: Affinity chromatography on Protein A

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

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

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

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu Acox2

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

Andere Bezeichnung: ACOX2 (Acox2 Produkte)

Synonyme: BCOX antikoerper, BRCACOX antikoerper, BRCOX antikoerper, THCCox antikoerper, THCA antikoerper, acyl-CoA oxidase 2 antikoerper, acyl-CoA oxidase 2, branched chain L homeolog antikoerper, acyl-CoA oxidase 2, branched chain antikoerper, acyl-Coenzyme A oxidase 2, branched chain antikoerper, ACOX2 antikoerper, acox2.L antikoerper, acox2 antikoerper, Acox2 antikoerper

Hintergrund: 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

Gen-ID: 8309

NCBI Accession: NP_003491

Pathways: Monocarboxylic Acid Catabolic Process