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GFAP Protein (AA 7-66) (Fc Tag)

GFAP Origin: Human Host: HEK-293 Cells Recombinant The purity of the protein is greater than 95 % as determined by SDS-PAGE and Coomassie blue staining.
Catalog No. ABIN7092818
  • Target See all GFAP Proteins
    GFAP (Glial Fibrillary Acidic Protein (GFAP))
    Protein Type
    Recombinant
    Protein Characteristics
    AA 7-66
    Origin
    • 10
    • 7
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    Human
    Source
    • 16
    • 5
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This GFAP protein is labelled with Fc Tag.
    Purpose
    Recombinant Human GFAP(7-66) with C-terminal human Fc tag
    Specificity
    GFAP (Thr7-Arg66) hFc (Glu99-Ala330)
    Characteristics
    Extracellular Domain Protein
    Purification
    Purified from cell culture supernatant by affinity chromatography
    Purity
    The purity of the protein is greater than 95 % as determined by SDS-PAGE and Coomassie blue staining.
    Top Product
    Discover our top product GFAP Protein
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Buffer
    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.
    Storage
    -20 °C,-80 °C
    Storage Comment
    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.
    Expiry Date
    12 months
  • Target
    GFAP (Glial Fibrillary Acidic Protein (GFAP))
    Alternative Name
    GFAP (GFAP Products)
    Synonyms
    GFAP Protein, AI836096 Protein, cb345 Protein, etID36982.3 Protein, gfapl Protein, wu:fb34h11 Protein, wu:fk42c12 Protein, xx:af506734 Protein, zgc:110485 Protein, glial fibrillary acidic protein Protein, GFAP Protein, LOC100136168 Protein, gfap Protein, Gfap Protein
    Background
    This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
    Molecular Weight
    predicted molecular mass of 32.4 kDa after removal of the signal peptide. The apparent molecular mass of GFAP(7-66)-hFc is 35-55 kDa due to glycosylation.
    UniProt
    P14136
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