TBL1X Monoclonal Antibody

活动价:

¥880.00

市场价:¥1280.00

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产品规格:
  • 50μL
货号:

FAB2600876

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商品描述
  • 靶点-Target

    TBL1X

  • 反应性

    Human,Monkey

  • 应用

    WB,ELISA

  • 宿主物种-Host Species

    Mouse

  • 修饰-Modification

    Unmodified

  • MW(Calculated)

    62kD

  • 推荐稀释比

    WB 1:500-1:2000;ELISA 1:10000;Not yet tested in other applications.

  • 组成

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

  • 纯化工艺

    Affinity purification

  • 储存

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

  • 克隆性

    Monoclonal

  • 免疫原

    Purified recombinant fragment of human TBL1X expressed in E. Coli.

  • 特异性

    TBL1X Monoclonal Antibody detects endogenous levels of TBL1X protein.

  • 基因名称

    TBL1X

  • 蛋白名称

    F-box-like/WD repeat-containing protein TBL1X

  • 别名

    TBL1X;TBL1;F-box-like/WD repeat-containing protein TBL1X;SMAP55;Transducin beta-like protein 1X;Transducin-beta-like protein 1;X-linked

  • Organism-1

    Human

  • 基因ID-1

    6907

  • SwissProt-1

    O60907

  • Organism-2

    Mouse

  • SwissProt-2

    Q9QXE7

  • 背景

    The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have bee

  • 细胞定位

    Nucleus . Colocalized with MECP2 to the heterochromatin foci. .