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L2HGDH Antikörper

L2HGDH Reaktivität: Human, Maus WB, IF Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN6293250
  • Target Alle L2HGDH Antikörper anzeigen
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    Reaktivität
    • 31
    • 15
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 36
    Kaninchen
    Klonalität
    • 36
    Polyklonal
    Konjugat
    • 18
    • 6
    • 4
    • 4
    • 2
    • 2
    Dieser L2HGDH Antikörper ist unkonjugiert
    Applikation
    • 26
    • 25
    • 9
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein of human L2HGDH
    Isotyp
    IgG
    Top Product
    Discover our top product L2HGDH Primärantikörper
  • Applikationshinweise
    WB 1:500 - 1:2000
    IF 1:50 - 1:200
    Kommentare

    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

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    PBS with 0.02 % sodium azide, 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.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20C. Avoid freeze / thaw cycles.
  • 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
    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
    50.316 kDa
    Gen-ID
    79944
    UniProt
    Q9H9P8
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