Glucose-6-Phosphate Dehydrogenase Antikörper (Middle Region)

Produktnummer ABIN631813

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch Glucose-6-Phosphate Dehydrogenase in WB. Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für Glucose-6-Phosphate Dehydrogenase Antikörper (Middle Region) (ABIN631813)

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)

Produktdetails anti-Glucose-6-Phosphate Dehydrogenase Antikörper

Bindungsspezifität: Middle Region

Spezifität: G6 PD antibody was raised against the middle region of G6 D

Aufreinigung: Affinity purified

Immunogen: G6 PD antibody was raised using the middle region of G6 D corresponding to a region with amino acids VTKNIHESCMSQIGWNRIIVEKPFGRDLQSSDRLSNHISSLFREDQIYRI

Anwendungsinformationen

Applikationshinweise: WB: 1 µg/mL
Optimal conditions should be determined by the investigator.

Kommentare:

G6PD Blocking Peptide, (ABIN5613685), is also available for use as a blocking control in assays to test for specificity of this G6PD antibody

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Lyophilized powder. Add distilled water for a 1 mg/mL concentration of G0 D antibody in PBS

Konzentration: Lot specific

Buffer: PBS

Handhabung: Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.

Details zu Glucose-6-Phosphate Dehydrogenase

Target: Glucose-6-Phosphate Dehydrogenase (G6PD)

Andere Bezeichnung: G6PD

Hintergrund: G6PD is a 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.

Molekulargewicht: 57 kDa (MW of target protein)

Pathways: Regulation of Systemic Arterial Blood Pressure by Hormones