Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

L2HGDH Protein (Myc-DYKDDDDK Tag)

L2HGDH Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2719817
  • Antigène Voir toutes L2HGDH Protéines
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Type de proteíne
    Recombinant
    Origine
    • 4
    • 2
    Humain
    Source
    • 4
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette L2HGDH protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Duranin 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 L2HGDH 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
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Autre désignation
    Duranin (L2HGDH Produits)
    Synonymes
    RGD1306250 Protein, C14orf160 Protein, BC016226 Protein, L-2-hydroxyglutarate dehydrogenase Protein, L2hgdh Protein, L2HGDH Protein
    Sujet
    This gene encodes L-2-hydroxyglutarate dehydrogenase, a FAD-dependent enzyme that oxidizes L-2-hydroxyglutarate to alpha-ketoglutarate in a variety of mammalian tissues. Mutations in this gene cause L-2-hydroxyglutaric aciduria, a rare autosomal recessive neurometabolic disorder resulting in moderate to severe mental retardation.
    Poids moléculaire
    45.2 kDa
    NCBI Accession
    NP_079160
Vous êtes ici:
Support technique