EHMT1 Monoclonal Antibody

活动价:

¥880.00

市场价:¥1280.00

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产品规格:
  • 50μL
货号:

FAB2600592

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商品描述
  • 靶点-Target

    EHMT1

  • 反应性

    Human

  • 应用

    WB,ELISA

  • 宿主物种-Host Species

    Mouse

  • 修饰-Modification

    Unmodified

  • MW(Calculated)

    141kD

  • 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 EHMT1 expressed in E. Coli.

  • 特异性

    EHMT1 Monoclonal Antibody detects endogenous levels of EHMT1 protein.

  • 基因名称

    EHMT1

  • 蛋白名称

    Histone-lysine N-methyltransferase, H3 lysine-9 specific 5

  • 别名

    EHMT1;EUHMTASE1;GLP;KIAA1876;KMT1D;Histone-lysine N-methyltransferase EHMT1;Euchromatic histone-lysine N-methyltransferase 1;Eu-HMTase1;G9a-like protein 1;GLP;GLP1;Histone H3-K9 methyltransferase 5;H3-K9-HMTase 5;Lysine N-methy

  • Organism-1

    Human

  • 基因ID-1

    79813

  • SwissProt-1

    Q9H9B1

  • Organism-2

    Mouse

  • SwissProt-2

    Q5DW34

  • 背景

    The protein encoded by this gene is a histone methyltransferase that is part of the E2F6 complex, which represses transcription. The encoded protein methylates the Lys-9 position of histone H3, which tags it for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014],

  • 细胞定位

    Nucleus. Chromosome. Associates with euchromatic regions.