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MOG Protein (AA 29-156) (His tag)

MOG Spezies: Maus Wirt: HEK-293 Cells Recombinant > 95 % as determined by Tris-Bis PAGE
Produktnummer ABIN7504467
  • Target Alle MOG Proteine anzeigen
    MOG (Myelin Oligodendrocyte Glycoprotein (MOG))
    Protein-Typ
    Recombinant
    Proteineigenschaft
    AA 29-156
    Spezies
    • 12
    • 6
    • 2
    • 1
    Maus
    Quelle
    • 11
    • 4
    • 2
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses MOG Protein ist gelabelt mit His tag.
    Verwendungszweck
    Mouse MOG/Myelin Oligodendrocyte Glycoprotein Protein
    Sequenz
    Gly29-Thr156
    Produktmerkmale
    Recombinant Mouse MOG/Myelin Oligodendrocyte Glycoprotein Protein is expressed from HEK293 with His tag at the C-Terminus.It contains Gly29-Thr156.
    Reinheit
    > 95 % as determined by Tris-Bis PAGE
    Sterilität
    0.22 μm filtered
    Endotoxin-Niveau
    Less than 1EU per μg by the LAL method.
    Top Product
    Discover our top product MOG Protein
  • Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Centrifuge the tube before opening. Reconstituting to a concentration more than 100 μg/mL is recommended. Dissolve the lyophilized protein in distilled water.
    Buffer
    Lyophilized from 0.22 μm filtered solution in PBS ( pH 7.4). Normally 8 % trehalose is added as protectant before lyophilization.
    Lagerung
    -20 °C,-80 °C
    Informationen zur Lagerung
    -20 to -80°C for 12 months as supplied from date of receipt., -80°C for 3-6 months after reconstitution., 2-8°C for 2-7 days after reconstitution., Recommend to aliquot the protein into smaller quantities for optimal storage. Please minimize freeze-thaw cycles.
    Haltbarkeit
    12 months
  • Target
    MOG (Myelin Oligodendrocyte Glycoprotein (MOG))
    Andere Bezeichnung
    MOG (MOG Produkte)
    Synonyme
    MOGIG2 Protein, NRCLP7 Protein, B230317G11Rik Protein, MOG Protein, myelin oligodendrocyte glycoprotein Protein, MOG Protein, Mog Protein
    Hintergrund
    Myelin oligodendrocyte glycoprotein (MOG) antibody disease is a rare autoimmune disorder with antibodies against the MOG predominantly involving the optic nerve and spinal cord leading to vision loss and paralysis. When MOG antibody disease involves the brain, the phenotype is similar to acute disseminated encephalomyelitis (ADEM).
    Molekulargewicht
    15.68 kDa. Due to glycosylation, the protein migrates to 18-25 kDa based on Tris-Bis PAGE result.
    UniProt
    Q61885
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