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NAA10 antibody (AA 111-235)

This anti-NAA10 antibody is a Mouse Monoclonal antibody detecting NAA10 in WB, ELISA, ICC and FACS. Suitable for Human, Mouse and Monkey.
Catalog No. ABIN5611234

Quick Overview for NAA10 antibody (AA 111-235) (ABIN5611234)

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
Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS)

Clone

3G3B9
  • 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

    FCM: 1/200 - 1/400

    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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