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GDAP1 anticorps

GDAP1 Reactivité: Souris, Humain, Rat WB, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7262477
  • Antigène Voir toutes GDAP1 Anticorps
    GDAP1 (Ganglioside-Induced Differentiation-Associated Protein 1 (GDAP1))
    Reactivité
    • 26
    • 14
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Souris, Humain, Rat
    Hôte
    • 28
    • 1
    Lapin
    Clonalité
    • 29
    Polyclonal
    Conjugué
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp GDAP1 est non-conjugé
    Application
    • 22
    • 13
    • 13
    • 7
    • 3
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human GDAP1 (NP_001035808.1).
    Isotype
    IgG
  • Indications d'application
    WB 1:500-1:2000 IHC 1:50-1:200
    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
    GDAP1 (Ganglioside-Induced Differentiation-Associated Protein 1 (GDAP1))
    Autre désignation
    GDAP1 (GDAP1 Produits)
    Synonymes
    anticorps CMT4, anticorps CMT4A, anticorps CMTRIA, anticorps ganglioside induced differentiation associated protein 1, anticorps ganglioside-induced differentiation-associated-protein 1, anticorps GDAP1, anticorps Gdap1
    Sujet
    This gene encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. Mutations in this gene have been associated with various forms of Charcot-Marie-Tooth Disease and neuropathy. Two transcript variants encoding different isoforms and a noncoding variant have been identified for this gene.
    Poids moléculaire

    Observed_MW: 38 kDa

    Calculated_MW: 33 kDa/41 kDa

    ID gène
    54332
    UniProt
    Q8TB36
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