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Fanconi Anemia Complementation Group G (FANCG) (Middle Region) Peptide

FANCG Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5671574
  • Antigène Tous les produits FANCG
    FANCG (Fanconi Anemia Complementation Group G (FANCG))
    Protein Region
    Middle Region
    Origine
    Humain
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    KSDAALQQLR AAALISRGLE WVASGQDTKA LQDFLLSVQM CPGNRDTYFH
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti- FANCG Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    FANCG (Fanconi Anemia Complementation Group G (FANCG))
    Synonymes
    xFANCG Peptide, FAG Peptide, XRCC9 Peptide, AU041407 Peptide, Xrcc9 Peptide, Fanconi anemia complementation group G S homeolog Peptide, Fanconi anemia complementation group G Peptide, Fanconi anemia, complementation group G Peptide, fancg.S Peptide, FANCG Peptide, Fancg Peptide
    Sujet
    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.

    Alias Symbols: FAG, XRCC9

    Protein Size: 622
    ID gène
    2189
    NCBI Accession
    NM_004629, NP_004620
    UniProt
    O15287
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