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ACADL 抗体 (N-Term)

This anti-ACADL antibody is a 兔 多克隆 antibody detecting ACADL in WB 和 IHC (p). Suitable for 人.
产品编号 ABIN2854767
发货至: 中国

Quick Overview for ACADL 抗体 (N-Term) (ABIN2854767)

抗原

See all ACADL 抗体
ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

适用

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  • 1
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宿主

  • 67
  • 1

克隆类型

  • 68
多克隆

标记

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This ACADL antibody is un-conjugated

应用范围

  • 49
  • 31
  • 26
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  • 7
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  • 5
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 15
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    N-Term

    交叉反应

    产品特性

    Rabbit Polyclonal antibody to ACADL (acyl-CoA dehydrogenase, long chain)
    ACADL antibody [N1N2], N-term

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the N-terminus region of human ACADL. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: H1299 , HCT116

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): 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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

    别名

    acyl-CoA dehydrogenase long chain

    背景

    The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.

    Cellular Localization: Mitochondrion matrix

    分子量

    48 kDa

    基因ID

    33

    UniProt

    P28330

    途径

    Monocarboxylic Acid Catabolic Process
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