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WTX anticorps

AMER1 Reactivité: Humain, Souris ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7238951
  • Antigène Voir toutes WTX (AMER1) Anticorps
    WTX (AMER1) (APC Membrane Recruitment Protein 1 (AMER1))
    Reactivité
    • 26
    • 16
    • 4
    Humain, Souris
    Hôte
    • 41
    Lapin
    Clonalité
    • 41
    Polyclonal
    Conjugué
    • 7
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp WTX est non-conjugé
    Application
    • 26
    • 26
    • 20
    • 8
    • 6
    • 6
    • 2
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human AMER1
    Isotype
    IgG
    Top Product
    Discover our top product AMER1 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    WTX (AMER1) (APC Membrane Recruitment Protein 1 (AMER1))
    Autre désignation
    AMER1 (AMER1 Produits)
    Synonymes
    anticorps 2810002O09Rik, anticorps AW492303, anticorps Fam123b, anticorps Wtx, anticorps FAM123B, anticorps OSCS, anticorps WTX, anticorps RGD1560322, anticorps fam123b, anticorps APC membrane recruitment 1, anticorps APC membrane recruitment protein 1, anticorps Amer1, anticorps AMER1, anticorps amer1
    Sujet
    The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts witHuman, Mouseany other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).
    NCBI Accession
    NP_689637
    UniProt
    Q5JTC6
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