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WB analysis of various sample lysates using GTX64704 ARD1A antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX64704 ARD1A antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX64704 ARD1A antibody. Dilution : 1:1000 Loading : 25microg per lane

ARD1A antibody

GTX64704
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetNAA10
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Overview

  • Supplier
    GeneTex
  • Product Name
    ARD1A antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. ICC/IF: 1:50 - 1:100. IHC-P: 1:50 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID8260
  • Target name
    NAA10
  • Target description
    N-alpha-acetyltransferase 10, NatA catalytic subunit
  • Target synonyms
    ARD1; ARD1 homolog A, N-acetyltransferase; ARD1A; ARD1P; arrest defective protein 1; DXS707; hARD1; MCOPS1; N-acetyltransferase ARD1, human homolog of; N-alpha-acetyltransferase 10; natA catalytic subunit Naa10; NATD; N-terminal acetyltransferase complex ARD1 subunit homolog A; OGDNS; TE2
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP41227
  • Protein Name
    N-alpha-acetyltransferase 10
  • Scientific Description
    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. [provided by RefSeq, Jan 2012]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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