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NAA10 antibody (AA 111-235)

The Mouse Monoclonal anti-NAA10 antibody has been validated for WB, ELISA and ICC. It is suitable to detect NAA10 in samples from Human, Mouse and Monkey.
Catalog No. ABIN5611233

Quick Overview for NAA10 antibody (AA 111-235) (ABIN5611233)

Target

See all NAA10 (ARD1A) Antibodies
NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))

Reactivity

  • 19
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Monkey

Host

  • 15
  • 4
Mouse

Clonality

  • 18
  • 1
Monoclonal

Conjugate

  • 12
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NAA10 antibody is un-conjugated

Application

  • 11
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Immunocytochemistry (ICC)

Clone

3G3E9
  • Binding Specificity

    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 111-235

    Purpose

    NAA10 Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human NAA10 (AA: 111-235) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    ICC: 1/200 - 1/1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))

    Alternative Name

    NAA10

    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.

    Molecular Weight

    26.5 kDa

    UniProt

    P41227
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