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ACOX1 抗体 (N-Term)

Cited in 1 publication. This 兔 多克隆 anti-ACOX1 antibody (Clone RB04649) specifically detects ACOX1 in IHC (p). The antibody is reactive with 人 和 小鼠 samples.
产品编号 ABIN389099
发货至: 中国
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Quick Overview for ACOX1 抗体 (N-Term) (ABIN389099)

抗原

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

适用

  • 66
  • 31
  • 14
人, 小鼠

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

  • 50
  • 34
  • 21
  • 16
  • 9
  • 3
  • 2
  • 2
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

克隆位点

RB04649
  • 抗原表位

    • 8
    • 7
    • 5
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 7-37, N-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 7-37 amino acids from the N-terminal region of human ACOX1.

    亚型

    Ig Fraction
  • 应用备注

    IHC-P: 1:10~50

    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
  • Bagattin, Hugendubler, Mueller: "Transcriptional coactivator PGC-1alpha promotes peroxisomal remodeling and biogenesis." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Issue 47, pp. 20376-81, (2010) (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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