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TAT Protein (Myc-DYKDDDDK Tag)

TAT Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2733246
  • Antigène Voir toutes TAT Protéines
    TAT (tyrosine Aminotransferase (TAT))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 4
    • 3
    HEK-293 Cells
    Purification/Conjugué
    Cette TAT protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human TAT (Tyrosine aminotransferase) 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 TAT 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
    TAT (tyrosine Aminotransferase (TAT))
    Autre désignation
    Tat (Tyrosine Aminotransferase) (TAT Produits)
    Synonymes
    MGC89628 Protein, wu:fb60g09 Protein, zgc:154059 Protein, si:ch211-238a12.1 Protein, F27C12.23 Protein, F27C12_23 Protein, TAT Protein, TYROSINE AMINOTRANSFERASE Protein, tyrosine aminotransferase 3 Protein, tyrosine aminotransferase Protein, tyrosine aminotransferase 3 Protein, TAT Protein, Tat Protein, tat Protein, TAT3 Protein
    Sujet
    This nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked.
    Poids moléculaire
    50.2 kDa
    NCBI Accession
    NP_000344
    Pathways
    Response to Water Deprivation
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