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MEGF10 anticorps

MEGF10 Reactivité: Humain, Souris, Rat IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6566961
  • Antigène Voir toutes MEGF10 Anticorps
    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 25
    Lapin
    Clonalité
    • 25
    Polyclonal
    Conjugué
    • 6
    • 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
    • 1
    Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human MEGF10 (NP_001295048.1).
    Isotype
    IgG
    Top Product
    Discover our top product MEGF10 Anticorps primaire
  • 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.
    Poids moléculaire

    Observed_MW: 115kDa

    Calculated_MW: 60kDa/122kDa

    ID gène
    84466
    UniProt
    Q96KG7
    Pathways
    Regulation of Muscle Cell Differentiation
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