Acox2 anticorps (C-Term)

N° du produit ABIN5516231

Cet anticorps anti-Acox2 Polyclonal Lapin (ABIN5516231) détecte spécifiquement Acox2 dans WB. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Acox2 anticorps (C-Term) (ABIN5516231)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Acox2 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Acox2 anticorps

Épitope: C-Term

Fonction: ACOX2 Antibody - C-terminal region

Séquence: DQCLNSALGC YDGNVYERLF QWAQKSPTNT QENPAYEEYI RPLLQSWRSK

Attributs du produit: This is a rabbit polyclonal antibody against ACOX2. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the C-terminal region of Human ACOX2

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP73731-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Détails sur Acox2

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

Autre désignation: ACOX2

Sujet:

Background Information: 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.

Alternative Symbols: BCOX, BRCOX, CBAS6, THCCox, BRCACOX

Poids moléculaire: 74kDa

ID gène: 8309

NCBI Accession: XP_005265562

UniProt: Q99424

Pathways: Monocarboxylic Acid Catabolic Process