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NAA10 antibody (AA 161-235)

This anti-NAA10 antibody is a Rabbit Polyclonal antibody detecting NAA10 in WB, IHC and IF. Suitable for Human.
Catalog No. ABIN6144318

Quick Overview for NAA10 antibody (AA 161-235) (ABIN6144318)

Target

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

Reactivity

  • 19
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 14
  • 5
Rabbit

Clonality

  • 17
  • 2
Polyclonal

Conjugate

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

Application

  • 11
  • 5
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 161-235

    Sequence

    HLELKEKGRH VVLGAIENKV ESKGNSPPSS GEACREEKGL AAEDSGGDSK DLSEVSETTE STDVKDSSEA SDSAS

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 161-235 of human NAA10 (NP_003482.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

    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.,NAA10,ARD1,ARD1A,ARD1P,DXS707,MCOPS1,NATD,OGDNS,TE2,Epigenetics & Nuclear Signaling,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,NAA10

    Molecular Weight

    24 kDa/26 kDa

    Gene ID

    8260

    UniProt

    P41227
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