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MEGF10 anticorps

MEGF10 Reactivité: Humain, Souris, Rat IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7255341
  • Antigène Voir toutes MEGF10 Anticorps
    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 24
    Lapin
    Clonalité
    • 24
    Polyclonal
    Conjugué
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MEGF10 est non-conjugé
    Application
    • 13
    • 13
    • 7
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human MEGF10 (NP_001295048.1).
    Isotype
    IgG
  • Indications d'application
    IF 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
    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))
    Autre désignation
    MEGF10 (MEGF10 Produits)
    Synonymes
    anticorps EMARDD, anticorps 3000002B06Rik, anticorps Gm331, anticorps multiple EGF-like domains 10, anticorps multiple EGF like domains 10, anticorps multiple EGF-like-domains 10, anticorps Megf10, anticorps MEGF10
    Sujet
    This gene encodes a member of the multiple epidermal growth factor-like domains protein family. The encoded protein plays a role in cell adhesion, motility and proliferation, and is a critical mediator of apoptotic cell phagocytosis as well as amyloid-beta peptide uptake in the brain. Expression of this gene may be associated with schizophrenia, and mutations in this gene are a cause of early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD) as well as congenital myopathy with minicores. Alternatively spliced transcript variants have been observed for this gene.
    ID gène
    84466
    UniProt
    Q96KG7
    Pathways
    Regulation of Muscle Cell Differentiation
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