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ACOX1 抗体 (AA 7-37)

ACOX1 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5647683
发货至: 中国
  • 抗原 See all ACOX1 抗体
    ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
    抗原表位
    • 9
    • 9
    • 8
    • 7
    • 5
    • 5
    • 1
    • 1
    • 1
    • 1
    AA 7-37
    适用
    • 71
    • 21
    • 3
    人, 小鼠
    宿主
    • 66
    • 6
    克隆类型
    • 56
    • 16
    多克隆
    标记
    • 32
    • 8
    • 8
    • 6
    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ACOX1 antibody is un-conjugated
    应用范围
    • 56
    • 48
    • 18
    • 16
    • 8
    • 3
    • 3
    • 2
    ELISA, Immunohistochemistry (IHC)
    纯化方法
    Purified
    免疫原
    A portion of amino acids 7-37 from the human protein was used as the immunogen for this ACOX1 antibody.
    亚型
    Ig Fraction
    Top Product
    Discover our top product ACOX1 Primary Antibody
  • 应用备注
    IHC (Paraffin): 1:10-1:50
    限制
    仅限研究用
  • 缓冲液
    In 1X PBS, pH 7.4, with 0.09 % sodium azide
    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
    Aliquot the ACOX1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 抗原
    ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
    别名
    ACOX1 / Peroxisomal acyl-coenzyme A oxidase 1 (ACOX1 产品)
    别名
    zgc:92584 antibody, wu:fb59h12 antibody, zgc:114033 antibody, aco antibody, acox antibody, ACOX antibody, PALMCOX antibody, SCOX antibody, RATACOA1 antibody, AOX antibody, Acox antibody, D130055E20Rik antibody, Paox antibody, PCOX1 antibody, acyl-CoA oxidase 1 antibody, acyl-CoA oxidase 1, palmitoyl antibody, acyl-CoA oxidase 1, palmitoyl L homeolog antibody, acyl-Coenzyme A oxidase 1, palmitoyl antibody, ACOX1 antibody, acox1 antibody, acox1.L antibody, Acox1 antibody
    背景
    ACOX1 is the first enzyme of the fatty acid beta-oxidation pathway, which catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids.
    UniProt
    Q15067
    途径
    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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