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ACOX1 抗体 (AA 605-648) (Fluoro647)

The 兔 多克隆 anti-ACOX1 antibody is suitable to detect ACOX1 in samples from 人, 小鼠 和 大鼠. It has been validated for FACS.
产品编号 ABIN7966109
发货至: 中国
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Quick Overview for ACOX1 抗体 (AA 605-648) (Fluoro647) (ABIN7966109)

抗原

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

适用

人, 小鼠, 大鼠

宿主

  • 74
  • 7

克隆类型

  • 58
  • 23
多克隆

标记

  • 37
  • 7
  • 6
  • 5
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ACOX1 antibody is conjugated to Fluoro647

应用范围

  • 56
  • 38
  • 25
  • 21
  • 10
  • 7
  • 4
  • 3
  • 2
Flow Cytometry (FACS)
  • 抗原表位

    • 11
    • 8
    • 8
    • 5
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 605-648

    原理

    Anti-ACOX1 Antibody Fluoro647 Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins

    预测反应

    Human ACOX1shares 93.2%,90.9% amino acid (aa) sequence identity with mouse,rat ACOX1,respectively.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human ACOX1 recombinant protein (Position: A605-E648). Human ACOX1shares 93.2% and 90.9% amino acid (aa) sequence identity with mouse and rat ACOX1, respectively.

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

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

    别名

    ACOX1

    背景

    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.

    Gene Full Name: acyl-CoA oxidase 1

    基因ID

    51

    UniProt

    Q15067

    途径

    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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