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CRTAP Protein (Myc-DYKDDDDK Tag)

CRTAP Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2712569
  • Target See all CRTAP Proteins
    CRTAP (Cartilage Associated Protein (CRTAP))
    Protein Type
    Recombinant
    Origin
    • 4
    • 3
    • 1
    Human
    Source
    • 4
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This CRTAP protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human CRTAP 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 CRTAP 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
    CRTAP (Cartilage Associated Protein (CRTAP))
    Alternative Name
    Crtap (CRTAP Products)
    Synonyms
    zgc:85621 Protein, wu:fb47h01 Protein, CASP Protein, LEPREL3 Protein, OI7 Protein, 5730529N23Rik Protein, Leprel3 Protein, RGD1565180 Protein, cartilage associated protein Protein, cartilage-associated protein Protein, crtap Protein, CRTAP Protein, LOC5574430 Protein, CpipJ_CPIJ013810 Protein, Crtap Protein
    Background
    The protein encoded by this gene is similar to the chicken and mouse CRTAP genes. The encoded protein is a scaffolding protein that may influence the activity of at least one member of the cytohesin/ARNO family in response to specific cellular stimuli. Defects in this gene are associated with osteogenesis imperfecta, a connective tissue disorder characterized by bone fragility and low bone mass.
    Molecular Weight
    43.9 kDa
    NCBI Accession
    NP_006362
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