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PGD Protein (AA 1-483) (His tag)

PGD Spezies: Human Wirt: Escherichia coli (E. coli) Recombinant > 95 % as determined by reducing SDS-PAGE.
Produktnummer ABIN7505267
  • Target Alle PGD Proteine anzeigen
    PGD (Phosphogluconate Dehydrogenase (PGD))
    Protein-Typ
    Recombinant
    Proteineigenschaft
    AA 1-483
    Spezies
    • 7
    • 1
    • 1
    • 1
    • 1
    Human
    Quelle
    • 4
    • 4
    • 2
    • 1
    Escherichia coli (E. coli)
    Aufreinigungstag / Konjugat
    Dieses PGD Protein ist gelabelt mit His tag.
    Sequenz
    Met 1-Ala 483
    Produktmerkmale
    A DNA sequence encoding the Human PGD protein (P52209) (Met 1-Ala 483) was expressed with a N-His&C-His.
    Reinheit
    > 95 % as determined by reducing SDS-PAGE.
    Top Product
    Discover our top product PGD Protein
  • Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Buffer
    Lyophilized from sterile PBS, pH 7.4.
    Normally 5 % - 8 % trehalose, mannitol and 0.01 % Tween80 are added as protectants before lyophilization.
    Lagerung
    4 °C,-20 °C,-80 °C
    Informationen zur Lagerung
    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
    Haltbarkeit
    12 months
  • Target
    PGD (Phosphogluconate Dehydrogenase (PGD))
    Andere Bezeichnung
    PGD (PGD Produkte)
    Hintergrund

    Abbreviation: PGD

    Target Synonym: 6-phosphogluconate dehydrogenase,Decarboxylating,PGD,PGDH,6PGD

    Background: 6-phosphogluconate dehydrogenase(PGD) is a cytoplasm-located protein, and belongs to the 6-phosphogluconate dehydrogenase family. 6PGD is the second dehydrogenase in the pentose phosphate shunt. It catalyzes the oxidative decarboxylation of 6-phosphogluconate to ribulose 5-phosphate and CO2, with concomitant reduction of NADP to NADPH. Mutations within the gene coding this enzyme result in 6-phosphogluconate dehydrogenase deficiency, an autosomal hereditary disease effecting the red blood cells.

    Molekulargewicht

    Calculated MW: 53.02 kDa

    Observed MW: 55 kDa

    UniProt
    P52209
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