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ACOX1 抗体 (C-Term)

This anti-ACOX1 antibody is a 兔 多克隆 antibody detecting ACOX1 in WB. Suitable for 人. This Primary Antibody has been cited in 1 publication.
产品编号 ABIN389100
发货至: 中国

Quick Overview for ACOX1 抗体 (C-Term) (ABIN389100)

抗原

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

适用

  • 57
  • 21
  • 3

宿主

  • 52
  • 6

克隆类型

  • 46
  • 12
多克隆

标记

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  • 5
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  • 3
  • 1
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  • 1
  • 1
  • 1
This ACOX1 antibody is un-conjugated

应用范围

  • 41
  • 34
  • 17
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  • 9
  • 4
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  • 2
Western Blotting (WB)

克隆位点

RB04651-04652
  • 抗原表位

    • 8
    • 7
    • 5
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 629-659, C-Term

    纯化方法

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    免疫原

    This ACOX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 629-659 amino acids from the C-terminal region of human ACOX1.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000. WB: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal 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
  • Gyamfi, Wan: "Mechanisms of resistance of hepatocyte retinoid X receptor alpha-null mice to WY-14,643-induced hepatocyte proliferation and cholestasis." in: The Journal of biological chemistry, Vol. 284, Issue 14, pp. 9321-30, (2009) (PubMed).

  • 抗原

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

    别名

    ACOX1

    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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