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L2HGDH Antikörper

L2HGDH Reaktivität: Human, Maus, Ratte ELISA, WB, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5703596
  • Target Alle L2HGDH Antikörper anzeigen
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Reaktivität
    • 30
    • 14
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 35
    Kaninchen
    Klonalität
    • 35
    Polyklonal
    Konjugat
    • 17
    • 6
    • 4
    • 4
    • 2
    • 2
    Dieser L2HGDH Antikörper ist unkonjugiert
    Applikation
    • 25
    • 24
    • 8
    • 2
    • 1
    ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
    Immunogen
    L-2-hydroxyglutarate dehydrogenase
    Isotyp
    IgG
    Top Product
    Discover our top product L2HGDH Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Kommentare

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

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    PBS with 0.02 % sodium azide and 50 % glycerol  pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handhabung
    Avoid repeated freeze / thaw cycles.
    Lagerung
    -20 °C
    Haltbarkeit
    12 months
  • Target
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Andere Bezeichnung
    L2HGDH (L2HGDH Produkte)
    Synonyme
    RGD1306250 antikoerper, C14orf160 antikoerper, BC016226 antikoerper, L-2-hydroxyglutarate dehydrogenase antikoerper, L2hgdh antikoerper, L2HGDH antikoerper
    Hintergrund
    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.
    Molekulargewicht
    46-48 kDa
    Gen-ID
    79944
    UniProt
    Q9H9P8
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