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NAA10 Protein (Myc-DYKDDDDK Tag)

ARD1A Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2726749
  • Antigène Voir toutes NAA10 (ARD1A) Protéines
    NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    • 1
    Humain
    Source
    • 1
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette NAA10 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human NAA10 / ARD1A 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 ARD1A 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
    NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))
    Autre désignation
    Naa10,ard1a (ARD1A Produits)
    Synonymes
    ARD1 Protein, ARD1A Protein, DXS707 Protein, NATD Protein, TE2 Protein, 2310039H09Rik Protein, Ard1 Protein, Ard1a Protein, Te2 Protein, RGD1565315 Protein, N(alpha)-acetyltransferase 10, NatA catalytic subunit Protein, NAA10 Protein, Naa10 Protein
    Sujet
    N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes an N-terminal acetyltransferase that functions as the catalytic subunit of the major amino-terminal acetyltransferase A complex. Mutations in this gene are the cause of Ogden syndrome. Alternate splicing results in multiple transcript variants.
    Poids moléculaire
    26.3 kDa
    NCBI Accession
    NP_003482
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