Glucose-6-Phosphate Dehydrogenase anticorps (Middle Region)

N° du produit ABIN631813

Cet anticorps Lapin Polyclonal détecte spécifiquement Glucose-6-Phosphate Dehydrogenase dans WB. Il présente une réactivité envers Humain.

Aperçu rapide pour Glucose-6-Phosphate Dehydrogenase anticorps (Middle Region) (ABIN631813)

Antigène: Glucose-6-Phosphate Dehydrogenase (G6PD)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

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

Application: Western Blotting (WB)

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

Épitope: Middle Region

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

Purification: Affinity purified

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

Information d'application

Indications d'application: WB: 1 µg/mL
Optimal conditions should be determined by the investigator.

Commentaires:

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

Restrictions: For Research Use only

Stockage

Format: Lyophilized

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

Concentration: Lot specific

Buffer: PBS

Conseil sur la manipulation: Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.

Détails sur Glucose-6-Phosphate Dehydrogenase

Antigène: Glucose-6-Phosphate Dehydrogenase (G6PD)

Autre désignation: G6PD

Sujet: 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.

Poids moléculaire: 57 kDa (MW of target protein)

Pathways: Regulation of Systemic Arterial Blood Pressure by Hormones