Glucose-6-Phosphate Dehydrogenase anticorps

N° du produit ABIN7880879

Cet anticorps Lapin Monoclonal détecte spécifiquement Glucose-6-Phosphate Dehydrogenase dans WB. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour Glucose-6-Phosphate Dehydrogenase anticorps (ABIN7880879)

Antigène: Glucose-6-Phosphate Dehydrogenase (G6PD)

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp Glucose-6-Phosphate Dehydrogenase est non-conjugé

Application: Western Blotting (WB)

Clone: ABBI-7

Détail du produit anti-Glucose-6-Phosphate Dehydrogenase anticorps

Fonction: G6PD Antibody / Glucose-6-phosphate dehydrogenase

Purification: Affinity purified

Immunogène: A synthetic peptide specific to human Glucose 6 Phosphate Dehydrogenase / G6PD was used as the immunogen for the G6PD antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the G6PD antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Antibody in PBS with 0.02 % sodium azide, 50 % glycerol and 0.4-0.5 mg/mL BSA

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: Store the G6PD antibody at -20oC.

Détails sur Glucose-6-Phosphate Dehydrogenase

Antigène: Glucose-6-Phosphate Dehydrogenase (G6PD)

Autre désignation: G6PD

Sujet: The G6PD gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene. [RefSeq]

UniProt: P11413

Pathways: Regulation of Systemic Arterial Blood Pressure by Hormones