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L2HGDH anticorps

L2HGDH Reactivité: Humain, Souris WB, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6293250
  • Antigène Voir toutes L2HGDH Anticorps
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Reactivité
    • 31
    • 15
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 36
    Lapin
    Clonalité
    • 36
    Polyclonal
    Conjugué
    • 18
    • 6
    • 4
    • 4
    • 2
    • 2
    Cet anticorp L2HGDH est non-conjugé
    Application
    • 26
    • 25
    • 9
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human L2HGDH
    Isotype
    IgG
    Top Product
    Discover our top product L2HGDH Anticorps primaire
  • Indications d'application
    WB 1:500 - 1:2000
    IF 1:50 - 1:200
    Commentaires

    Widely expressed, Highly expressed in brain, testis and muscle, Expressed to a lower extent in lymphocytes, fibroblasts, keratinocytes, placenta, bladder, small intestine, liver and bone marrow

    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide, 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.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20C. Avoid freeze / thaw cycles.
  • 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
    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
    50.316 kDa
    ID gène
    79944
    UniProt
    Q9H9P8
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