Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

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

PGD Origin: Human Host: Escherichia coli (E. coli) Recombinant > 95 % as determined by reducing SDS-PAGE.
Catalog No. ABIN7505267
  • Target See all PGD Proteins
    PGD (Phosphogluconate Dehydrogenase (PGD))
    Protein Type
    Recombinant
    Protein Characteristics
    AA 1-483
    Origin
    • 7
    • 1
    • 1
    • 1
    • 1
    Human
    Source
    • 4
    • 4
    • 2
    • 1
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This PGD protein is labelled with His tag.
    Sequence
    Met 1-Ala 483
    Characteristics
    A DNA sequence encoding the Human PGD protein (P52209) (Met 1-Ala 483) was expressed with a N-His&C-His.
    Purity
    > 95 % as determined by reducing SDS-PAGE.
    Top Product
    Discover our top product PGD Protein
  • Restrictions
    For Research Use only
  • 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.
    Storage
    4 °C,-20 °C,-80 °C
    Storage Comment
    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.
    Expiry Date
    12 months
  • Target
    PGD (Phosphogluconate Dehydrogenase (PGD))
    Alternative Name
    PGD (PGD Products)
    Background

    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.

    Molecular Weight

    Calculated MW: 53.02 kDa

    Observed MW: 55 kDa

    UniProt
    P52209
You are here:
Support