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Emerin Protein (EMD) (Myc-DYKDDDDK Tag)

EMD Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2720155
  • Antigène Voir toutes Emerin (EMD) Protéines
    Emerin (EMD)
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 1
    Humain
    Source
    • 2
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette Emerin protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Emerin protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product EMD Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    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.
    Stock
    -80 °C
    Stockage commentaire
    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.
  • Antigène
    Emerin (EMD)
    Autre désignation
    Emerin (EMD Produits)
    Synonymes
    fj58f01 Protein, wu:fj58f01 Protein, EMD Protein, Bocks Protein, Bocksbeutel Protein, CG9424 Protein, Dmel\\CG9424 Protein, emerin Protein, emd Protein, xemd1 Protein, xemerin2 Protein, xemd2 Protein, xemerin1 Protein, EDMD Protein, LEMD5 Protein, STA Protein, AW550900 Protein, Sta Protein, emerin Protein, emerin (Emery-Dreifuss muscular dystrophy) Protein, bocksbeutel Protein, emerin L homeolog Protein, emerin S homeolog Protein, EMD Protein, emd Protein, bocks Protein, emd.L Protein, emd.S Protein, Emd Protein
    Sujet
    Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene.
    Poids moléculaire
    28.8 kDa
    NCBI Accession
    NP_000108
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