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NAA10 antibody

ARD1A Reactivity: Human, Mouse, Rat IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7262951
  • Target See all NAA10 (ARD1A) Antibodies
    NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))
    Reactivity
    • 19
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 15
    • 4
    Rabbit
    Clonality
    • 18
    • 1
    Polyclonal
    Conjugate
    • 12
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NAA10 antibody is un-conjugated
    Application
    • 11
    • 4
    • 3
    • 3
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human NAA10 (NP_003482.1).
    Isotype
    IgG
    Top Product
    Discover our top product ARD1A Primary Antibody
  • Application Notes
    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
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))
    Alternative Name
    NAA10 (ARD1A Products)
    Synonyms
    ARD1 antibody, ARD1A antibody, DXS707 antibody, NATD antibody, TE2 antibody, 2310039H09Rik antibody, Ard1 antibody, Ard1a antibody, Te2 antibody, RGD1565315 antibody, N(alpha)-acetyltransferase 10, NatA catalytic subunit antibody, NAA10 antibody, Naa10 antibody
    Background
    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.
    Gene ID
    8260
    UniProt
    P41227
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