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FKRP Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

FKRP Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2721451
  • Antigène Voir toutes FKRP Protéines
    FKRP (Fukutin Related Protein (FKRP))
    Type de proteíne
    Recombinant
    Attributs du protein
    Transcript Variant 1
    Origine
    • 3
    • 2
    Humain
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette FKRP protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Fukutin-related protein (transcript variant 1) 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 FKRP 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
    FKRP (Fukutin Related Protein (FKRP))
    Autre désignation
    Fukutin-Related Protein (FKRP Produits)
    Synonymes
    zgc:162829 Protein, LGMD2I Protein, MDC1C Protein, MDDGA5 Protein, MDDGB5 Protein, MDDGC5 Protein, A830029B19Rik Protein, AI842067 Protein, AI847300 Protein, LGMD1I Protein, fukutin related protein Protein, FKRP Protein, fkrp Protein, Fkrp Protein
    Sujet
    This gene encodes a protein which is targeted to the medial Golgi apparatus and is necessary for posttranslational modification of dystroglycan. Mutations in this gene have been associated with congenital muscular dystrophy, mental retardation, and cerebellar cysts. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
    Poids moléculaire
    54.4 kDa
    NCBI Accession
    NP_077277
    Pathways
    Regulation of Carbohydrate Metabolic Process
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