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L2HGDH anticorps

L2HGDH Reactivité: Humain, Souris, Rat ELISA, WB, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5703596
  • Antigène Voir toutes L2HGDH Anticorps
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Reactivité
    • 30
    • 14
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 35
    Lapin
    Clonalité
    • 35
    Polyclonal
    Conjugué
    • 17
    • 6
    • 4
    • 4
    • 2
    • 2
    Cet anticorp L2HGDH est non-conjugé
    Application
    • 25
    • 24
    • 8
    • 2
    • 1
    ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
    Immunogène
    L-2-hydroxyglutarate dehydrogenase
    Isotype
    IgG
    Top Product
    Discover our top product L2HGDH Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Commentaires

    mouse small intestine tissue were subjected to SDS PAGE followed by western blot with FNab04670(L2HGDH antibody) at dilution of 1:800

    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide and 50 % glycerol  pH 7.3
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Conseil sur la manipulation
    Avoid repeated freeze / thaw cycles.
    Stock
    -20 °C
    Date de péremption
    12 months
  • Antigène
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Autre désignation
    L2HGDH (L2HGDH Produits)
    Synonymes
    anticorps RGD1306250, anticorps C14orf160, anticorps BC016226, anticorps L-2-hydroxyglutarate dehydrogenase, anticorps L2hgdh, anticorps L2HGDH
    Sujet
    Synonyms:C14orf160 Background: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
    46-48 kDa
    ID gène
    79944
    UniProt
    Q9H9P8
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