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AF4 anticorps

AFF1 Reactivité: Humain, Rat IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6570791
  • Antigène Tous les produits AF4 (AFF1)
    AF4 (AFF1) (AF4/FMR2 Family, Member 1 (AFF1))
    Reactivité
    • 45
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Rat
    Hôte
    • 43
    • 2
    Lapin
    Clonalité
    • 43
    • 2
    Polyclonal
    Conjugué
    • 21
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp AF4 est non-conjugé
    Application
    • 24
    • 19
    • 13
    • 13
    • 9
    • 5
    • 4
    • 3
    • 3
    • 1
    • 1
    Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human AFF1 (NP_001160165.1).
    Isotype
    IgG
  • 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
    AF4 (AFF1) (AF4/FMR2 Family, Member 1 (AFF1))
    Autre désignation
    AFF1 (AFF1 Produits)
    Synonymes
    anticorps AF4, anticorps MLLT2, anticorps PBM1, anticorps 9630032B01Rik, anticorps AW319193, anticorps Af4, anticorps Mllt2h, anticorps Rob, anticorps Mllt2, anticorps AF4/FMR2 family member 1, anticorps AF4/FMR2 family, member 1, anticorps AFF1, anticorps Aff1
    Sujet
    This gene encodes a member of the AF4/ lymphoid nuclear protein related to AF4/Fragile X E mental retardation syndrome family of proteins, which have been implicated in childhood lymphoblastic leukemia, Fragile X E site mental retardation, and ataxia. It is the prevalent mixed-lineage leukemia fusion gene associated with spontaneous acute lymphoblastic leukemia. Members of this family have three conserved domains: an N-terminal homology domain, an AF4/ lymphoid nuclear protein related to AF4/Fragile X E mental retardation syndrome domain, and a C-terminal homology domain. The protein functions as a regulator of RNA polymerase II-mediated transcription through elongation and chromatin remodeling functions. Through RNA interference screens, this gene has been shown to promote the expression of CD133, a plasma membrane glycoprotein required for leukemia cell survival. Alternative splicing results in multiple transcript variants.
    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 131kDa/132kDa

    ID gène
    4299
    UniProt
    P51825
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