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COL8a2 Protein (Myc-DYKDDDDK Tag)

COL8A2 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2712429
  • Target Alle COL8a2 (COL8A2) Proteine anzeigen
    COL8a2 (COL8A2) (Collagen, Type VIII, alpha 2 (COL8A2))
    Protein-Typ
    Recombinant
    Spezies
    • 3
    • 3
    Human
    Quelle
    • 3
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses COL8a2 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human Collagen type VIII alpha 2 chain 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 COL8A2 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
    COL8a2 (COL8A2) (Collagen, Type VIII, alpha 2 (COL8A2))
    Andere Bezeichnung
    Collagen Type VIII alpha 2 Chain (COL8A2 Produkte)
    Synonyme
    FECD Protein, FECD1 Protein, PPCD Protein, PPCD2 Protein, AI429819 Protein, collagen type VIII alpha 2 chain Protein, collagen, type VIII, alpha 2 Protein, COL8A2 Protein, Col8a2 Protein
    Hintergrund
    This gene encodes the alpha 2 chain of type VIII collagen. This protein is a major component of the basement membrane of the corneal endothelium and forms homo- or heterotrimers with alpha 1 (VIII) type collagens. Defects in this gene are associated with Fuchs endothelial corneal dystrophy and posterior polymorphous corneal dystrophy type 2. Alternative splicing results in multiple transcript variants.
    Molekulargewicht
    64.4 kDa
    NCBI Accession
    NP_005193
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