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COL6A2 Protein (Myc-DYKDDDDK Tag)

COL6A2 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2712426
  • Antigène Voir toutes COL6A2 Protéines
    COL6A2 (Collagen, Type VI, alpha 2 (COL6A2))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 1
    Humain
    Source
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette COL6A2 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Collagen type VI alpha 2 chain (transcript variant 2C2) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product COL6A2 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    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.
  • Antigène
    COL6A2 (Collagen, Type VI, alpha 2 (COL6A2))
    Autre désignation
    Collagen Type VI alpha 2 Chain (COL6A2 Produits)
    Synonymes
    PP3610 Protein, Col6a-2 Protein, collagen type VI alpha 2 chain Protein, collagen, type VI, alpha 2 Protein, COL6A2 Protein, col6a2 Protein, Tcur_3411 Protein, Col6a2 Protein
    Sujet
    This gene encodes one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The product of this gene contains several domains similar to von Willebrand Factor type A domains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in this gene are associated with Bethlem myopathy and Ullrich scleroatonic muscular dystrophy. Three transcript variants have been identified for this gene.
    Poids moléculaire
    106.5 kDa
    NCBI Accession
    NP_001840
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