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Six5 Protein (Myc-DYKDDDDK Tag)

SIX5 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2732100
  • Antigène Voir toutes Six5 (SIX5) Protéines
    Six5 (SIX5) (Homeobox protein SIX5 (SIX5))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    Humain
    Source
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette Six5 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human SIX5 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 SIX5 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
    Six5 (SIX5) (Homeobox protein SIX5 (SIX5))
    Autre désignation
    Six5 (SIX5 Produits)
    Synonymes
    Dmahp Protein, MDMAHP Protein, TrexBF Protein, BOR2 Protein, DMAHP Protein, sine oculis-related homeobox 5 Protein, SIX homeobox 5 Protein, Six5 Protein, SIX5 Protein
    Sujet
    The protein encoded by this gene is a homeodomain-containing transcription factor that appears to function in the regulation of organogenesis. This gene is located downstream of the dystrophia myotonica-protein kinase gene. Mutations in this gene are a cause of branchiootorenal syndrome type 2.
    Poids moléculaire
    74.4 kDa
    NCBI Accession
    NP_787071
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