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FANCG Antikörper

FANCG Reaktivität: Human ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN2423431
  • Target Alle FANCG Antikörper anzeigen
    FANCG (Fanconi Anemia Complementation Group G (FANCG))
    Reaktivität
    • 64
    • 4
    • 2
    Human
    Wirt
    • 59
    • 4
    • 1
    Kaninchen
    Klonalität
    • 62
    • 2
    Polyklonal
    Konjugat
    • 26
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Dieser FANCG Antikörper ist unkonjugiert
    Applikation
    • 62
    • 28
    • 26
    • 26
    • 18
    • 9
    • 6
    • 4
    • 3
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein of human FANCG
    Isotyp
    IgG
    Top Product
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  • Applikationshinweise
    IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Konservierungsmittel
    Sodium azide
    Handhabung
    Avoid freeze / thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    FANCG (Fanconi Anemia Complementation Group G (FANCG))
    Andere Bezeichnung
    FANCG (FANCG Produkte)
    Synonyme
    xFANCG antikoerper, FAG antikoerper, XRCC9 antikoerper, AU041407 antikoerper, Xrcc9 antikoerper, Fanconi anemia complementation group G S homeolog antikoerper, Fanconi anemia complementation group G antikoerper, Fanconi anemia, complementation group G antikoerper, fancg.S antikoerper, FANCG antikoerper, Fancg antikoerper
    Hintergrund
    The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity, they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group G.
    Pathways
    DNA Reparatur
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