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Glucose-6-Phosphate Dehydrogenase anticorps

L’anticorps Lapin Polyclonal anti-Glucose-6-Phosphate Dehydrogenase a été validé pour IF. Il convient pour détecter Glucose-6-Phosphate Dehydrogenase dans des échantillons de Humain et Souris.
N° du produit ABIN7257547

Aperçu rapide pour Glucose-6-Phosphate Dehydrogenase anticorps (ABIN7257547)

Antigène

Voir toutes Glucose-6-Phosphate Dehydrogenase (G6PD) Anticorps
Glucose-6-Phosphate Dehydrogenase (G6PD)

Reactivité

  • 88
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  • 2
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  • 1
Humain, Souris

Hôte

  • 115
  • 15
  • 12
Lapin

Clonalité

  • 118
  • 24
Polyclonal

Conjugué

  • 73
  • 22
  • 9
  • 6
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  • 3
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  • 2
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  • 2
  • 1
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Cet anticorp Glucose-6-Phosphate Dehydrogenase est non-conjugé

Application

  • 104
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  • 50
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  • 9
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Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

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

    Glucose-6-Phosphate Dehydrogenase (G6PD)

    Autre désignation

    G6PD

    Sujet

    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.

    ID gène

    2539

    UniProt

    P11413

    Pathways

    Regulation of Systemic Arterial Blood Pressure by Hormones
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