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GFAP Protein (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
    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
    affinity purification
    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
    Reconstitution
    Reconstitute with deionized water
    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
    Synonymes: ALXDRD
    Description: 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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