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ACOX1 抗体

ACOX1 适用: 人 WB, IF, IHC (p) 宿主: 小鼠 Monoclonal 153CT43-1-1 unconjugated
产品编号 ABIN659022
发货至: 中国
  • 抗原 See all ACOX1 抗体
    ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
    适用
    • 62
    • 22
    • 3
    宿主
    • 57
    • 6
    小鼠
    克隆类型
    • 47
    • 16
    单克隆
    标记
    • 33
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    This ACOX1 antibody is un-conjugated
    应用范围
    • 46
    • 39
    • 19
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    Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    This antibody is purified through a protein G column, followed by dialysis against PBS.
    免疫原
    This ACOX1 monoclonal antibody is generated from mouse immunized with ACOX1 recombinant protein.
    克隆位点
    153CT43-1-1
    亚型
    IgG1
    Top Product
    Discover our top product ACOX1 Primary Antibody
  • 应用备注
    IF: 1:10~50. WB: 1:4000. IHC-P: 1:10~50
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) 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
    4 °C,-20 °C
    储存方法
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    有效期
    6 months
  • 抗原
    ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
    别名
    ACOX1 (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.
    分子量
    74424
    基因ID
    51
    NCBI登录号
    NP_001171968, NP_004026, NP_009223
    UniProt
    Q15067
    途径
    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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