Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

COL8a2 Protein (Myc-DYKDDDDK Tag)

COL8A2 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2712429
  • Target See all COL8a2 (COL8A2) Proteins
    COL8a2 (COL8A2) (Collagen, Type VIII, alpha 2 (COL8A2))
    Protein Type
    Recombinant
    Origin
    • 3
    • 3
    Human
    Source
    • 3
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This COL8a2 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Collagen type VIII alpha 2 chain 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 COL8A2 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
    COL8a2 (COL8A2) (Collagen, Type VIII, alpha 2 (COL8A2))
    Alternative Name
    Collagen Type VIII alpha 2 Chain (COL8A2 Products)
    Synonyms
    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
    Background
    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.
    Molecular Weight
    64.4 kDa
    NCBI Accession
    NP_005193
You are here:
Support