Glucose-6-Phosphate Dehydrogenase antibody

Catalog No. ABIN7880879

This Rabbit Monoclonal antibody specifically detects Glucose-6-Phosphate Dehydrogenase in WB. It exhibits reactivity toward Human.

Quick Overview for Glucose-6-Phosphate Dehydrogenase antibody (ABIN7880879)

Target: Glucose-6-Phosphate Dehydrogenase (G6PD)

Reactivity: Human

Host: Rabbit

Clonality: Monoclonal

Conjugate: This Glucose-6-Phosphate Dehydrogenase antibody is un-conjugated

Application: Western Blotting (WB)

Clone: ABBI-7

Product Details anti-Glucose-6-Phosphate Dehydrogenase Antibody

Purpose: G6PD Antibody / Glucose-6-phosphate dehydrogenase

Purification: Affinity purified

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

Isotype: IgG

Application Details

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

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store the G6PD antibody at -20oC.

Target Details for Glucose-6-Phosphate Dehydrogenase

Target: Glucose-6-Phosphate Dehydrogenase (G6PD)

Alternative Name: G6PD

Background: 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