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NAA10 anticorps

ARD1A Reactivité: Humain, Souris, Rat IHC, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6570853
  • Antigène Voir toutes NAA10 (ARD1A) Anticorps
    NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))
    Reactivité
    • 20
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 16
    • 4
    Lapin
    Clonalité
    • 19
    • 1
    Polyclonal
    Conjugué
    • 13
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp NAA10 est non-conjugé
    Application
    • 11
    • 5
    • 4
    • 4
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human NAA10 (NP_003482.1).
    Isotype
    IgG
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    Discover our top product ARD1A Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200 IF 1:50-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))
    Autre désignation
    NAA10 (ARD1A Produits)
    Synonymes
    anticorps ARD1, anticorps ARD1A, anticorps DXS707, anticorps NATD, anticorps TE2, anticorps 2310039H09Rik, anticorps Ard1, anticorps Ard1a, anticorps Te2, anticorps RGD1565315, anticorps N(alpha)-acetyltransferase 10, NatA catalytic subunit, anticorps NAA10, anticorps Naa10
    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

    Observed_MW: 26kDa

    Calculated_MW: 24kDa/26kDa

    ID gène
    8260
    UniProt
    P41227
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