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RASD2 Protein (Myc-DYKDDDDK Tag)

RASD2 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2730533
  • Antigène Voir toutes RASD2 Protéines
    RASD2 (RASD Family, Member 2 (RASD2))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 2
    • 2
    • 1
    Humain
    Source
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette RASD2 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human RASD2 / TEM2 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 RASD2 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
    RASD2 (RASD Family, Member 2 (RASD2))
    Autre désignation
    Rasd2,tem2 (RASD2 Produits)
    Synonymes
    RASD2 Protein, MGC:4834 Protein, Rhes Protein, TEM2 Protein, 4930526B11Rik Protein, AU045414 Protein, TEM-2 Protein, RASD family member 2 Protein, RASD family, member 2 Protein, RASD2 Protein, Rasd2 Protein
    Sujet
    This gene belongs to the Ras superfamily of small GTPases and is enriched in the striatum. The encoded protein functions as an E3 ligase for attachment of small ubiquitin-like modifier (SUMO). This protein also binds to mutant huntingtin (mHtt), the protein mutated in Huntington disease (HD). Sumoylation of mHTT by this protein may cause degeneration of the striatum. The protein functions as an activator of mechanistic target of rapamycin 1 (mTOR1), which in turn plays a role in myelination, axon growth and regeneration. Reduced levels of mRNA expressed by this gene were found in HD patients.
    Poids moléculaire
    30.2 kDa
    NCBI Accession
    NP_055125
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