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Smoothelin Protein (SMTN) (Transcript Variant 2) (Myc-DYKDDDDK Tag)

SMTN Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2732255
  • Target See all Smoothelin (SMTN) Proteins
    Smoothelin (SMTN)
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 2
    Origin
    • 3
    • 1
    • 1
    Human
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This Smoothelin protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Smoothelin (transcript variant 2) 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 SMTN 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
    Smoothelin (SMTN)
    Alternative Name
    Smoothelin (SMTN Products)
    Synonyms
    smsmo Protein, MGC68765 Protein, SMTN Protein, MGC140000 Protein, MGC155237 Protein, DKFZp468D019 Protein, smoothelin Protein, smoothelin L homeolog Protein, smoothelin b Protein, SMTN Protein, Smtn Protein, smtn.L Protein, smtnb Protein, smtn Protein
    Background
    This gene encodes a structural protein that is found exclusively in contractile smooth muscle cells. It associates with stress fibers and constitutes part of the cytoskeleton. This gene is localized to chromosome 22q12.3, distal to the TUPLE1 locus and outside the DiGeorge syndrome deletion. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms.
    Molecular Weight
    98.7 kDa
    NCBI Accession
    NP_599031
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