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FANCD2 Antikörper (Isoform B)

FANCD2 Reaktivität: Human, Maus IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN966127
  • Target Alle FANCD2 Antikörper anzeigen
    FANCD2 (Fanconi Anemia, Complementation Group D2 (FANCD2))
    Bindungsspezifität
    • 16
    • 15
    • 15
    • 8
    • 7
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Isoform B
    Reaktivität
    • 102
    • 25
    • 22
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 101
    • 2
    Kaninchen
    Klonalität
    • 91
    • 12
    Polyklonal
    Konjugat
    • 35
    • 8
    • 7
    • 7
    • 7
    • 7
    • 7
    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Dieser FANCD2 Antikörper ist unkonjugiert
    Applikation
    • 29
    • 27
    • 27
    • 24
    • 16
    • 14
    • 12
    • 9
    • 8
    • 7
    • 6
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Immunogen
    Polyclonal antibody produced in rabbits immunizing with a synthetic peptide corresponding to N-terminal residues of human FANCD2 (Fanconi anemia complementation group D2 isoform b)
    Top Product
    Discover our top product FANCD2 Primärantikörper
  • Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Lagerung
    4 °C
  • Kweekel, Antonini, Nortier, Punt, Gelderblom, Guchelaar: "Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array." in: British journal of cancer, Vol. 101, Issue 2, pp. 357-62, (2009) (PubMed).

    Singh, Bakker, Agarwal, Jansen, Grassman, Godthelp, Ali, Du, Rooimans, Fan, Wahengbam, Steltenpool, Andreassen, Williams, Joenje, de Winter, Meetei: "Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M." in: Blood, Vol. 114, Issue 1, pp. 174-80, (2009) (PubMed).

    Kuhnert, Kachnic, Li, Purschke, Gheorghiu, Lee, Held, Willers: "FANCD2-deficient human fibroblasts are hypersensitive to ionising radiation at oxygen concentrations of 0% and 3% but not under normoxic conditions." in: International journal of radiation biology, Vol. 85, Issue 6, pp. 523-31, (2009) (PubMed).

    Chan, Palmai-Pallag, Ying, Hickson: "Replication stress induces sister-chromatid bridging at fragile site loci in mitosis." in: Nature cell biology, Vol. 11, Issue 6, pp. 753-60, (2009) (PubMed).

  • Target
    FANCD2 (Fanconi Anemia, Complementation Group D2 (FANCD2))
    Andere Bezeichnung
    FANCD2 (FANCD2 Produkte)
    Synonyme
    FANCD2 antikoerper, CG17269 antikoerper, CG31192 antikoerper, CG31194 antikoerper, Dmel\\CG17269 antikoerper, dmFANCD2 antikoerper, xfancd2 antikoerper, FA-D2 antikoerper, FA4 antikoerper, FACD antikoerper, FAD antikoerper, FAD2 antikoerper, FANCD antikoerper, 2410150O07Rik antikoerper, AU015151 antikoerper, BB137857 antikoerper, Fanconi anemia complementation group D2 antikoerper, CG17269 gene product from transcript CG17269-RA antikoerper, Fanconi anemia group D2 protein antikoerper, Fanconi anemia, complementation group D2 antikoerper, Fanconi anemia complementation group D2 L homeolog antikoerper, FANCD2 antikoerper, Fancd2 antikoerper, LOC100455970 antikoerper, fancd2 antikoerper, fancd2.L 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). 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 D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA1 AND BRCA2) involved in homologydirected DNA repair. Alternative splicing results in two transcript variants encoding different isoforms.
    Pathways
    DNA Reparatur
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