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ACOX1 抗体 (AA 1-270)

The 兔 多克隆 anti-ACOX1 antibody (ABIN7111266) specifically detects ACOX1 in WB, IHC, ELISA 和 IF. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN7111266
发货至: 中国
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Quick Overview for ACOX1 抗体 (AA 1-270) (ABIN7111266)

抗原

See all ACOX1 抗体
ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))

适用

人, 小鼠, 大鼠

宿主

  • 62
  • 5

克隆类型

  • 47
  • 20
多克隆

标记

  • 32
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This ACOX1 antibody is un-conjugated

应用范围

  • 49
  • 33
  • 20
  • 15
  • 9
  • 3
  • 3
  • 2
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
  • 抗原表位

    • 8
    • 8
    • 5
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-270

    原理

    ACOX1 antibody

    纯化方法

    Immunogen affinity purified

    纯度

    ≥95 % as determined by SDS-PAGE

    免疫原

    Immunogen sequence: 1-270aa

    Immunogen: acyl-Coenzyme A oxidase 1, palmitoyl

    亚型

    IgG
  • 应用备注

    WB: 1:500 - 1:2000, IHC: 1:100 - 1:200, IF: 1:50 - 1:200

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide and 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.

    注意事项

    Avoid repeated freeze / thaw cycles.

    储存条件

    -20 °C

    储存方法

    -20°C for 12 months

    有效期

    12 months
  • 抗原

    ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))

    别名

    ACOX1

    背景

    Synonyms: Peroxisomal acyl-coenzyme A oxidase 1 (AOX)|Palmitoyl-CoA oxidase|Peroxisomal fatty acyl-CoA oxidase|Straight-chain acyl-CoA oxidase (SCOX)|Peroxisomal acyl-CoA oxidase 1, A chain|Peroxisomal acyl-CoA oxidase 1, B chain|Peroxisomal acyl-CoA oxidase 1, C chain|ACOX1|ACOX

    Background: 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.It has 3 isoforms produced by alternative splicing with the molecular mass of 70-74 kDa and can be cleaved post-translationally into a 50- kDa and a 22- kDa subunit between Val468 and Ala469 (PMID: 10672038).

    分子量

    74 kDa

    基因ID

    51

    UniProt

    Q15067

    途径

    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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