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D2HGDH Protein (Myc-DYKDDDDK Tag)

D2HGDH Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2712408
  • Antigène Voir toutes D2HGDH Protéines
    D2HGDH (D-2-Hydroxyglutarate Dehydrogenase (D2HGDH))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 2
    • 1
    • 1
    Humain
    Source
    • 3
    • 3
    HEK-293 Cells
    Purification/Conjugué
    Cette D2HGDH protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human D2HGDH / D2HGD protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product D2HGDH Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    D2HGDH (D-2-Hydroxyglutarate Dehydrogenase (D2HGDH))
    Autre désignation
    d2hgdh,d2hgd (D2HGDH Produits)
    Synonymes
    AA408776 Protein, AA408778 Protein, AI325464 Protein, RGD1307976 Protein, D2HGD Protein, zgc:158661 Protein, D-2-hydroxyglutarate dehydrogenase Protein, D2hgdh Protein, D2HGDH Protein, d2hgdh Protein
    Sujet
    This gene encodes D-2hydroxyglutarate dehydrogenase, a mitochondrial enzyme belonging to the FAD-binding oxidoreductase/transferase type 4 family. This enzyme, which is most active in liver and kidney but also active in heart and brain, converts D-2-hydroxyglutarate to 2-ketoglutarate. Mutations in this gene are present in D-2-hydroxyglutaric aciduria, a rare recessive neurometabolic disorder causing developmental delay, epilepsy, hypotonia, and dysmorphic features.
    Poids moléculaire
    54.8 kDa
    NCBI Accession
    NP_689996
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