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MOG Protein (AA 30-154) (His tag)

MOG Origin: Human Host: HEK-293 Cells Recombinant > 95 % as determined by Tris-Bis PAGE,> 95 % as determined by HPLC
Catalog No. ABIN7275275
  • Target See all MOG Proteins
    MOG (Myelin Oligodendrocyte Glycoprotein (MOG))
    Protein Type
    Recombinant
    Protein Characteristics
    AA 30-154
    Origin
    • 12
    • 7
    • 2
    • 1
    Human
    Source
    • 11
    • 5
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This MOG protein is labelled with His tag.
    Purpose
    Human MOG/Myelin Oligodendrocyte Glycoprotein Protein
    Sequence
    Gly30-Gly154
    Characteristics
    Recombinant Human MOG/Myelin Oligodendrocyte Glycoprotein Protein is expressed from HEK293 with His tag at the C-Terminus.It contains Gly30-Gly154.
    Purity
    > 95 % as determined by Tris-Bis PAGE,> 95 % as determined by HPLC
    Sterility
    0.22 μm filtered
    Endotoxin Level
    Less than 1EU per μg by the LAL method.
    Top Product
    Discover our top product MOG Protein
  • 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 0.22μm filtered solution in PBS ( pH 7.4). Normally 8 % trehalose is added as protectant before lyophilization.
    Storage
    -20 °C,-80 °C
    Storage Comment
    -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.
    Expiry Date
    12 months
  • Target
    MOG (Myelin Oligodendrocyte Glycoprotein (MOG))
    Alternative Name
    MOG (MOG Products)
    Synonyms
    MOGIG2 Protein, NRCLP7 Protein, B230317G11Rik Protein, MOG Protein, myelin oligodendrocyte glycoprotein Protein, MOG Protein, Mog Protein
    Background
    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).
    Molecular Weight
    15.4 kDa. Due to glycosylation, the protein migrates to 20-23 kDa based on Tris-Bis PAGE result.
    UniProt
    Q16653
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