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

MOG Origine: Souris Hôte: HEK-293 Cells Recombinant > 95 % as determined by Tris-Bis PAGE
N° du produit ABIN7504467
  • Antigène Voir toutes MOG Protéines
    MOG (Myelin Oligodendrocyte Glycoprotein (MOG))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 29-156
    Origine
    • 12
    • 6
    • 2
    • 1
    Souris
    Source
    • 11
    • 4
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette MOG protéine est marqué à la His tag.
    Fonction
    Mouse MOG/Myelin Oligodendrocyte Glycoprotein Protein
    Séquence
    Gly29-Thr156
    Attributs du produit
    Recombinant Mouse MOG/Myelin Oligodendrocyte Glycoprotein Protein is expressed from HEK293 with His tag at the C-Terminus.It contains Gly29-Thr156.
    Pureté
    > 95 % as determined by Tris-Bis PAGE
    Stérilité
    0.22 μm filtered
    niveau d'endotoxine
    Less than 1EU per μg by the LAL method.
    Top Product
    Discover our top product MOG Protéine
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    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.
    Stock
    -20 °C,-80 °C
    Stockage commentaire
    -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.
    Date de péremption
    12 months
  • Antigène
    MOG (Myelin Oligodendrocyte Glycoprotein (MOG))
    Autre désignation
    MOG (MOG Produits)
    Synonymes
    MOGIG2 Protein, NRCLP7 Protein, B230317G11Rik Protein, MOG Protein, myelin oligodendrocyte glycoprotein Protein, MOG Protein, Mog Protein
    Sujet
    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).
    Poids moléculaire
    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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