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Acox2 抗体 (AA 1-30)

Acox2 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5647636
发货至: 中国
  • 抗原 See all Acox2 抗体
    Acox2 (Acyl-CoA Oxidase 2, Branched Chain (Acox2))
    抗原表位
    • 15
    • 13
    • 7
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-30
    适用
    • 34
    • 26
    • 17
    宿主
    • 44
    • 4
    • 1
    克隆类型
    • 47
    • 2
    多克隆
    标记
    • 18
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This Acox2 antibody is un-conjugated
    应用范围
    • 25
    • 22
    • 13
    • 13
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA
    纯化方法
    Antigen affinity purified
    免疫原
    A portion of amino acids 1-30 from the human protein was used as the immunogen for this ACOX2 antibody.
    亚型
    Ig Fraction
    Top Product
    Discover our top product Acox2 Primary Antibody
  • 应用备注
    Western blot: 1:1000
    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 ACOX2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 抗原
    Acox2 (Acyl-CoA Oxidase 2, Branched Chain (Acox2))
    别名
    ACOX2 / Peroxisomal acyl-coenzyme A oxidase 2 (Acox2 产品)
    别名
    BCOX antibody, BRCACOX antibody, BRCOX antibody, THCCox antibody, THCA antibody, acyl-CoA oxidase 2 antibody, acyl-CoA oxidase 2, branched chain L homeolog antibody, acyl-CoA oxidase 2, branched chain antibody, acyl-Coenzyme A oxidase 2, branched chain antibody, ACOX2 antibody, acox2.L antibody, acox2 antibody, Acox2 antibody
    背景
    Peroxisomal acyl-coenzyme A oxidase 2 belongs to the acyl-CoA oxidase family. It encodes the branched-chain acyl-CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates, and may lead to Zellweger syndrome, severe mental retardation, and death in children.
    UniProt
    Q99424
    途径
    Monocarboxylic Acid Catabolic Process
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