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COL6A2 Protein (Myc-DYKDDDDK Tag)

COL6A2 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2712427
  • Target See all COL6A2 Proteins
    COL6A2 (Collagen, Type VI, alpha 2 (COL6A2))
    Protein Type
    Recombinant
    Origin
    • 4
    • 1
    Human
    Source
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This COL6A2 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Collagen type VI alpha 2 chain (transcript variant 2C2a) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product COL6A2 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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
    COL6A2 (Collagen, Type VI, alpha 2 (COL6A2))
    Alternative Name
    Collagen Type VI alpha 2 Chain (COL6A2 Products)
    Synonyms
    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
    Background
    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.
    Molecular Weight
    95.3 kDa
    NCBI Accession
    NP_478054
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