HADH anticorps (AA 43-301) (Cy3)

N° du produit ABIN7998621

Cet anticorps Lapin Polyclonal détecte spécifiquement HADH dans FACS. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour HADH anticorps (AA 43-301) (Cy3) (ABIN7998621)

Antigène: HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HADH est conjugé à/à la Cy3

Application: Flow Cytometry (FACS)

Détail du produit anti-HADH anticorps (Cy3)

Épitope: AA 43-301

Fonction: Anti-HADH Antibody Cy3 Conjugated

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

Homologie: Human HADH shares 90.3%,90.7% amino acid (aa) sequence identity with mouse,rat HADH,respectively.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human HADH recombinant protein (Position: A43-K301). Human HADH shares 90.3% and 90.7% amino acid (aa) sequence identity with mouse and rat HADH, respectively.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, 1-3 μg/1x10⁶ cells

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 HADH

Antigène: HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

Autre désignation: HADH

Sujet:

Background: Hydroxyacyl-Coenzyme A dehydrogenase (HADH) is an enzyme which in humans is encoded by the HADH gene. This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15.

Gene Full Name: hydroxyacyl-CoA dehydrogenase

ID gène: 3033

UniProt: Q16836

Pathways: Negative Regulation of Hormone Secretion, Monocarboxylic Acid Catabolic Process