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ACOX1 抗体

ACOX1 适用: 人, 小鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7264135
发货至: 中国
  • 抗原 See all ACOX1 抗体
    ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))
    适用
    • 59
    • 19
    • 3
    人, 小鼠
    宿主
    • 53
    • 6
    克隆类型
    • 44
    • 15
    多克隆
    标记
    • 29
    • 6
    • 6
    • 4
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ACOX1 antibody is un-conjugated
    应用范围
    • 43
    • 37
    • 18
    • 14
    • 7
    • 3
    • 2
    • 2
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human ACOX1 (NP_004026.2).
    亚型
    IgG
    Top Product
    Discover our top product ACOX1 Primary Antibody
  • 应用备注
    IHC 1:100-1:200 IF 1:50-1:200
    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
    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
    The protein encoded by this gene 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. Alternatively spliced transcript variants encoding different isoforms have been identified.
    基因ID
    51
    UniProt
    Q15067
    途径
    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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