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Dymeclin Protein (DYM) (Myc-DYKDDDDK Tag)

DYM Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2719847
  • Target Alle Dymeclin (DYM) Proteine anzeigen
    Dymeclin (DYM)
    Protein-Typ
    Recombinant
    Spezies
    • 3
    • 1
    Human
    Quelle
    • 2
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses Dymeclin Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human Dymeclin protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product DYM Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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
    Dymeclin (DYM)
    Andere Bezeichnung
    Dymeclin (DYM Produkte)
    Synonyme
    DYM Protein, LOC734107 Protein, dym Protein, DMC Protein, SMC Protein, 1810041M12Rik Protein, 4933427L07Rik Protein, C030019K18Rik Protein, RGD1309111 Protein, dymeclin Protein, dymeclin L homeolog Protein, DYM Protein, dym Protein, Dym Protein, dym.L Protein
    Hintergrund
    This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia, which involve both skeletal defects and mental retardation.
    Molekulargewicht
    75.8 kDa
    NCBI Accession
    NP_060123
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