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GFAP Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

GFAP Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2721841
  • Target Alle GFAP Proteine anzeigen
    GFAP (Glial Fibrillary Acidic Protein (GFAP))
    Protein-Typ
    Recombinant
    Proteineigenschaft
    Transcript Variant 1
    Spezies
    • 10
    • 7
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    Human
    Quelle
    • 16
    • 5
    • 2
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses GFAP Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human GFAP (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product GFAP Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    GFAP (Glial Fibrillary Acidic Protein (GFAP))
    Andere Bezeichnung
    Gfap (GFAP Produkte)
    Synonyme
    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
    Hintergrund
    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.
    Molekulargewicht
    49.7 kDa
    NCBI Accession
    NP_002046
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