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FANCM anticorps

FANCM Reactivité: Humain IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5963437
  • Antigène Voir toutes FANCM Anticorps
    FANCM (Fanconi Anemia Complementation Group M (FANCM))
    Reactivité
    • 28
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 26
    • 2
    • 1
    Lapin
    Clonalité
    • 29
    Polyclonal
    Conjugué
    • 15
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp FANCM est non-conjugé
    Application
    • 13
    • 13
    • 11
    • 8
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human FANCM (NP_065988.1).
    Isotype
    IgG
    Top Product
    Discover our top product FANCM Anticorps primaire
  • Indications d'application
    IF 1:50-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    FANCM (Fanconi Anemia Complementation Group M (FANCM))
    Autre désignation
    FANCM (FANCM Produits)
    Synonymes
    anticorps FAAP250, anticorps KIAA1596, anticorps AI427100, anticorps C730036B14Rik, anticorps D12Ertd364e, anticorps Fanconi anemia complementation group M, anticorps hypothetical protein, anticorps Fanconi anemia, complementation group M, anticorps FANCM, anticorps PGTG_17854, anticorps Fancm
    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 M. Alternative splicing results in multiple transcript variants.
    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 75kDa/229kDa/232kDa

    ID gène
    57697
    UniProt
    Q8IYD8
    Pathways
    Réparation de l'ADN
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