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Glucose-6-Phosphate Dehydrogenase antibody

The Rabbit Polyclonal anti-Glucose-6-Phosphate Dehydrogenase antibody is suitable to detect Glucose-6-Phosphate Dehydrogenase in samples from Human and Mouse. It has been validated for IF.
Catalog No. ABIN7257547
$696.00
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 15 Business Days

Quick Overview for Glucose-6-Phosphate Dehydrogenase antibody (ABIN7257547)

Target

See all Glucose-6-Phosphate Dehydrogenase (G6PD) Antibodies
Glucose-6-Phosphate Dehydrogenase (G6PD)

Reactivity

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Human, Mouse

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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

Application

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Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human G6PD (NP_000393.4).

    Isotype

    IgG
  • Application Notes

    IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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 at -20°C. Avoid freeze / thaw cycles.
  • Target

    Glucose-6-Phosphate Dehydrogenase (G6PD)

    Alternative Name

    G6PD

    Background

    This 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.

    Gene ID

    2539

    UniProt

    P11413

    Pathways

    Regulation of Systemic Arterial Blood Pressure by Hormones
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