AMPD1 Polyclonal Antibody

活动价:

¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2612783

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商品描述
  • 靶点-Target

    AMPD1

  • 反应性

    Human,Mouse,Rat

  • 应用

    IHC,IF,ELISA

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Unmodified

  • MW(Calculated)

    86kD

  • 推荐稀释比

    IHC 1:100-1:300;ELISA 1:40000;IF 1:50-200

  • 组成

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • 纯化工艺

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • 储存

    -15°C to -25°C/1 year(Do not lower than -25°C)

  • 浓度

    1 mg/ml

  • 克隆性

    Polyclonal

  • 免疫原

    The antiserum was produced against synthesized peptide derived from human AMPD1. AA range:261-310

  • 特异性

    AMPD1 Polyclonal Antibody detects endogenous levels of AMPD1 protein.

  • 基因名称

    AMPD1

  • 蛋白名称

    AMP deaminase 1

  • 别名

    AMPD1;AMP deaminase 1;AMP deaminase isoform M;Myoadenylate deaminase

  • Organism-1

    Human

  • 基因ID-1

    270

  • SwissProt-1

    P23109

  • Organism-2

    Mouse

  • SwissProt-2

    Q3V1D3

  • Organism-3

    Rat

  • 基因ID-3

    25028

  • SwissProt-3

    P10759

  • 背景

    Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010],

  • 细胞定位

    cytosol,