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GFAP Protein (His tag)

Recombinant GFAP-Protein exprimiert in Escherichia coli (E. coli).
Produktnummer ABIN7581228

Kurzübersicht für GFAP Protein (His tag) (ABIN7581228)

Target

Alle GFAP Proteine anzeigen
GFAP (Glial Fibrillary Acidic Protein (GFAP))

Protein-Typ

Recombinant

Spezies

  • 13
  • 10
  • 5
  • 4
  • 1
  • 1
  • 1
  • 1
Human

Quelle

  • 18
  • 5
  • 5
  • 2
  • 2
  • 1
Escherichia coli (E. coli)

Applikation

Antibody Production (AbP), Standard (STD)

Reinheit

> 80% as determined by SDS-PAGE and Coomassie blue staining
  • Aufreinigungstag / Konjugat

    Dieses GFAP Protein ist gelabelt mit His tag.

    Verwendungszweck

    GFAP Human Recombinant Protein

    Produktmerkmale

    Purified recombinant protein of Human glial fibrillary acidic protein (GFAP), transcript variant 1, Leu292-End, with N-terminal His tag, expressed in E.coli
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    Produkt
    Expressionssystem
    Konjugat
    Origin
    Preis ab
    Expressionssystem HEK-293 Cells
    Konjugat His tag
    Origin Human
    Preis ab 12.620,45 €
    Expressionssystem Cell-free protein synthesis (CFPS)
    Konjugat Strep Tag
    Origin Human
    Preis ab 20.480,57 €

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  • Applikationshinweise

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Kommentare

    For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    25 mM Tris-HCl, pH 8.0, 150 mM NaCl, 10% glycerol

    Lagerung

    -80 °C

    Informationen zur Lagerung

    Store at -80°C after receiving vials. Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.
  • Target

    GFAP (Glial Fibrillary Acidic Protein (GFAP))

    Andere Bezeichnung

    Gfap

    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

    16.4 kDa

    NCBI Accession

    NP_002046
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