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MEGF10 Antikörper

MEGF10 Reaktivität: Human, Maus, Ratte IF Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5967274
  • Target Alle MEGF10 Antikörper anzeigen
    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))
    Reaktivität
    Human, Maus, Ratte
    Wirt
    • 25
    Kaninchen
    Klonalität
    • 25
    Polyklonal
    Konjugat
    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser MEGF10 Antikörper ist unkonjugiert
    Applikation
    • 13
    • 13
    • 7
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human MEGF10 (NP_001295048.1).
    Isotyp
    IgG
    Top Product
    Discover our top product MEGF10 Primärantikörper
  • Applikationshinweise
    IF 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))
    Andere Bezeichnung
    MEGF10 (MEGF10 Produkte)
    Synonyme
    EMARDD antikoerper, 3000002B06Rik antikoerper, Gm331 antikoerper, multiple EGF-like domains 10 antikoerper, multiple EGF like domains 10 antikoerper, multiple EGF-like-domains 10 antikoerper, Megf10 antikoerper, MEGF10 antikoerper
    Hintergrund
    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.
    Molekulargewicht

    Observed_MW: 115kDa

    Calculated_MW: 60kDa/122kDa

    Gen-ID
    84466
    UniProt
    Q96KG7
    Pathways
    Regulation of Muscle Cell Differentiation
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