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GFAP Protein (AA 68-377) (His tag)

GFAP Origine: Humain Hôte: HEK-293 Cells Recombinant The purity of the protein is greater than 85 % as determined by SDS-PAGE and Coomassie blue staining.
N° du produit ABIN7092819
  • Antigène Voir toutes GFAP Protéines
    GFAP (Glial Fibrillary Acidic Protein (GFAP))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 68-377
    Origine
    • 10
    • 7
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 16
    • 5
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette GFAP protéine est marqué à la His tag.
    Fonction
    Recombinant human GFAP(68-377) protein with N-terminal 6xHis tag
    Specificité
    6xHis tag GFAP (Ser68-Ile377)
    Attributs du produit
    Extracellular Domain Protein
    Purification
    Purified from cell culture supernatant by affinity chromatography
    Pureté
    The purity of the protein is greater than 85 % as determined by SDS-PAGE and Coomassie blue staining.
    Top Product
    Discover our top product GFAP Protéine
  • 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.
    Stock
    -20 °C,-80 °C
    Stockage commentaire
    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.
    Date de péremption
    12 months
  • Antigène
    GFAP (Glial Fibrillary Acidic Protein (GFAP))
    Autre désignation
    GFAP (GFAP Produits)
    Synonymes
    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
    Sujet
    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]
    Poids moléculaire
    predicted molecular mass of 37.2 kDa after removal of the signal peptide. The apparent molecular mass of His-GFAP(68-377) is 35-55 kDa due to glycosylation.
    UniProt
    P14136
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