Glucose-6-Phosphate Dehydrogenase Antikörper

Produktnummer ABIN7880879

Dieser Kaninchen Monoklonal Antikörper detektiert spezifisch Glucose-6-Phosphate Dehydrogenase in WB. Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für Glucose-6-Phosphate Dehydrogenase Antikörper (ABIN7880879)

Target: Glucose-6-Phosphate Dehydrogenase (G6PD)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Monoklonal

Konjugat: Dieser Glucose-6-Phosphate Dehydrogenase Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Klon: ABBI-7

Produktdetails anti-Glucose-6-Phosphate Dehydrogenase Antikörper

Verwendungszweck: G6PD Antibody / Glucose-6-phosphate dehydrogenase

Aufreinigung: Affinity purified

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the G6PD antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store the G6PD antibody at -20oC.

Details zu Glucose-6-Phosphate Dehydrogenase

Target: Glucose-6-Phosphate Dehydrogenase (G6PD)

Andere Bezeichnung: G6PD

Hintergrund: 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