DYRK1A/B (Phospho Tyr321/273) rabbit pAb

活动价:

¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2612387

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商品描述
  • 靶点-Target

    DYRK1A/B

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Phospho

  • MW(Calculated)

    84kD

  • 推荐稀释比

    WB 1:500-2000

  • 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 serum by affinity-chromatography using 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 human DYRK1A/B (Phospho-Tyr321/273)

  • 特异性

    This antibody detects endogenous levels of DYRK1A/B (Phospho-Tyr321/273) at Human, Mouse,Rat

  • 基因名称

    DYRK1A DYRK MNB MNBH

  • 蛋白名称

    DYRK1A/B (Phospho-Tyr321/273)

  • 别名

    Dual specificity tyrosine-phosphorylation-regulated kinase 1A;Dual specificity YAK1-related kinase;HP86;Protein kinase minibrain homolog;MNBH;hMNB;

  • Organism-1

    Human

  • 基因ID-1

    1859

  • SwissProt-1

    Q13627

  • Organism-2

    Mouse

  • 基因ID-2

    13548

  • SwissProt-2

    Q61214

  • Organism-3

    Rat

  • 基因ID-3

    25255

  • SwissProt-3

    Q63470

  • 背景

    This gene encodes a member of the Dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) family. This member contains a nuclear targeting signal sequence, a protein kinase domain, a leucine zipper motif, and a highly conservative 13-consecutive-histidine repeat. It catalyzes its autophosphorylation on serine/threonine and tyrosine residues. It may play a significant role in a signaling pathway regulating cell proliferation and may be involved in brain development. This gene is a homolog of Drosophila mnb (minibrain) gene and rat Dyrk gene. It is localized in the Down syndrome critical region of chromosome 21, and is considered to be a strong candidate gene for learning defects associated with Down syndrome. Alternative splicing of this gene generates several transcript variants differing from each other either in the 5' UTR or in the 3' co

  • 细胞定位

    Nucleus . Nucleus speckle .