ACAD9 anticorps (AA 92-621) (Fluoro647)

N° du produit ABIN7966065

Cet anticorps anti-ACAD9 Polyclonal Lapin conjugué à Fluoro647 (ABIN7966065) détecte spécifiquement ACAD9 dans FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour ACAD9 anticorps (AA 92-621) (Fluoro647) (ABIN7966065)

Antigène: ACAD9 (Acyl-CoA Dehydrogenase Family, Member 9 (ACAD9))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACAD9 est conjugé à/à la Fluoro647

Application: Flow Cytometry (FACS)

Détail du produit anti-ACAD9 anticorps (Fluoro647)

Épitope: AA 92-621

Fonction: Anti-ACAD9 Antibody Fluoro647 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human ACAD9 recombinant protein (Position: K92-C621).

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur ACAD9

Antigène: ACAD9 (Acyl-CoA Dehydrogenase Family, Member 9 (ACAD9))

Autre désignation: ACAD9

Sujet:

Background: Acyl-CoA dehydrogenase family member 9, mitochondrial is an enzyme that in humans is encoded by the ACAD9 gene. This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.

Gene Full Name: acyl-CoA dehydrogenase family member 9

ID gène: 28976

UniProt: Q9H845

Pathways: SARS-CoV-2 Protein Interactome