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NAA10 抗体

ARD1A 适用: 人, 小鼠, 大鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7262951
发货至: 中国
  • 抗原 See all NAA10 (ARD1A) 抗体
    NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))
    适用
    • 19
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 15
    • 4
    克隆类型
    • 18
    • 1
    多克隆
    标记
    • 12
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NAA10 antibody is un-conjugated
    应用范围
    • 11
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human NAA10 (NP_003482.1).
    亚型
    IgG
    Top Product
    Discover our top product ARD1A Primary Antibody
  • 应用备注
    IHC 1:50-1:200 IF 1:50-1:100
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))
    别名
    NAA10 (ARD1A 产品)
    别名
    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
    背景
    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.
    基因ID
    8260
    UniProt
    P41227
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