AMPD3 Polyclonal Antibody

活动价:

¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2612785

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商品描述
  • 靶点-Target

    AMPD3

  • 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)

    89kD

  • 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

    Synthesized peptide derived from AMPD3 . at AA range: 280-360

  • 特异性

    AMPD3 Polyclonal Antibody detects endogenous levels of AMPD3 protein.

  • 基因名称

    AMPD3

  • 蛋白名称

    AMP deaminase 3

  • 别名

    AMPD3;AMP deaminase 3;AMP deaminase isoform E;Erythrocyte AMP deaminase

  • Organism-1

    Human

  • 基因ID-1

    272

  • SwissProt-1

    Q01432

  • Organism-2

    Mouse

  • 基因ID-2

    11717

  • SwissProt-2

    O08739

  • Organism-3

    Rat

  • 基因ID-3

    25095

  • SwissProt-3

    O09178

  • 背景

    This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008],

  • 细胞定位

    cytosol,