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Acox2 anticorps (N-Term)
L’anticorps Lapin Polyclonal anti-Acox2 a été validé pour WB et EIA. Il convient pour détecter Acox2 dans des échantillons de Humain.
Aperçu rapide pour Acox2 anticorps (N-Term) (ABIN950243)
Antigène
Voir toutes Acox2 Anticorps
Acox2
(Acyl-CoA Oxidase 2, Branched Chain (Acox2))
Reactivité
Toutes les réactivités sur Acox2 Anticorps
Humain
Hôte
Toutes les hôtes sur Acox2 Anticorps
Lapin
Clonalité
Toutes les clonalités sur Acox2 Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers Acox2 Anticorps
Cet anticorp Acox2 est non-conjugé
Application
Tous les applications à travers Acox2 Anticorps.
Western Blotting (WB), Enzyme Immunoassay (EIA)
Détail du produit anti-Acox2 anticorps
(cache)
Épitope
Tous les épitopes à travers Acox2 Anticorps.
AA 1-30, N-Term
Specificité
This antibody reacts to ACOX2.
Réactivité croisée (Details)
Species reactivity (tested):Human.
Purification
Affinity chromatography on Protein A
Immunogène
KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human ACOX2
Isotype
Ig Fraction
Alternatives
(show)
Information d'application
(cache)
Indications d'application
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Stockage
(cache)
Format
Liquid
Concentration
0.25 mg/mL
Buffer
PBS containing 0.09 % (W/V) sodium azide as preservative
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.
Conseil sur la manipulation
Avoid repeated freezing and thawing.
Stock
4 °C/-20 °C
Stockage commentaire
Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
Détails sur Acox2
(cache)
Antigène
Acox2
(Acyl-CoA Oxidase 2, Branched Chain (Acox2))
Autre désignation
ACOX2
Sujet
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
ID gène
8309
NCBI Accession
NP_003491
Pathways
Monocarboxylic Acid Catabolic Process
Vus récemment
(cache)
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