Glucose-6-Phosphate Dehydrogenase Antikörper (AA 297-326)

Produktnummer ABIN3031057

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch Glucose-6-Phosphate Dehydrogenase in WB, IHC, ELISA und FACS. Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für Glucose-6-Phosphate Dehydrogenase Antikörper (AA 297-326) (ABIN3031057)

Target: Glucose-6-Phosphate Dehydrogenase (G6PD)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

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

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)

Produktdetails anti-Glucose-6-Phosphate Dehydrogenase Antikörper

Bindungsspezifität: AA 297-326

Verwendungszweck: G6PD Antibody

Aufreinigung: Purified

Immunogen: A portion of amino acids 297-326 from the human protein was used as the immunogen for this G6PD antibody.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Titration of the G6PD antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

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: Aliquot the G6PD antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Details zu Glucose-6-Phosphate Dehydrogenase

Target: Glucose-6-Phosphate Dehydrogenase (G6PD)

Andere Bezeichnung: G6PD

Hintergrund: G6PD 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.

UniProt: P11413

Pathways: Regulation of Systemic Arterial Blood Pressure by Hormones