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Glucose-6-Phosphate Dehydrogenase Antikörper

Der Kaninchen Polyklonal Anti-Glucose-6-Phosphate Dehydrogenase-Antikörper wurde für IF validiert. Er ist geeignet, Glucose-6-Phosphate Dehydrogenase in Proben von Human und Maus zu detektieren.
Produktnummer ABIN7257547

Kurzübersicht für Glucose-6-Phosphate Dehydrogenase Antikörper (ABIN7257547)

Target

Alle Glucose-6-Phosphate Dehydrogenase (G6PD) Antikörper anzeigen
Glucose-6-Phosphate Dehydrogenase (G6PD)

Reaktivität

  • 88
  • 41
  • 22
  • 9
  • 7
  • 6
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Maus

Wirt

  • 115
  • 15
  • 12
Kaninchen

Klonalität

  • 118
  • 24
Polyklonal

Konjugat

  • 73
  • 22
  • 9
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Glucose-6-Phosphate Dehydrogenase Antikörper ist unkonjugiert

Applikation

  • 104
  • 51
  • 50
  • 31
  • 22
  • 20
  • 16
  • 15
  • 14
  • 14
  • 9
  • 8
  • 8
  • 7
  • 5
  • 4
  • 3
  • 1
Immunofluorescence (IF)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

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

    Isotyp

    IgG
  • Applikationshinweise

    IF 1:50-1:200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

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

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    Glucose-6-Phosphate Dehydrogenase (G6PD)

    Andere Bezeichnung

    G6PD

    Hintergrund

    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.

    Gen-ID

    2539

    UniProt

    P11413

    Pathways

    Regulation of Systemic Arterial Blood Pressure by Hormones
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