Clock Monoclonal Antibody

活动价:

¥880.00

市场价:¥1280.00

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产品规格:
  • 50μL
货号:

FAB2600559

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商品描述
  • 靶点-Target

    Clock

  • 反应性

    Human

  • 应用

    WB,IF,ELISA

  • 宿主物种-Host Species

    Mouse

  • 修饰-Modification

    Unmodified

  • MW(Calculated)

    95kD

  • 推荐稀释比

    WB 1:500-1:2000;IF 1:200-1:1000;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 Clock expressed in E. Coli.

  • 特异性

    Clock Monoclonal Antibody detects endogenous levels of Clock protein.

  • 基因名称

    CLOCK

  • 蛋白名称

    Circadian locomoter output cycles protein kaput

  • 别名

    CLOCK;BHLHE8;KIAA0334;Circadian locomoter output cycles protein kaput;hCLOCK;Class E basic helix-loop-helix protein 8;bHLHe8

  • Organism-1

    Human

  • 基因ID-1

    9575

  • SwissProt-1

    O15516

  • Organism-2

    Mouse

  • SwissProt-2

    O08785

  • 背景

    The protein encoded by this gene plays a central role in the regulation of circadian rhythms. The protein encodes a transcription factor of the basic helix-loop-helix (bHLH) family and contains DNA binding histone acetyltransferase activity. The encoded protein forms a heterodimer with ARNTL (BMAL1) that binds E-box enhancer elements upstream of Period (PER1, PER2, PER3) and Cryptochrome (CRY1, CRY2) genes and activates transcription of these genes. PER and CRY proteins heterodimerize and repress their own transcription by interacting in a feedback loop with CLOCK/ARNTL complexes. Polymorphisms in this gene may be associated with behavioral changes in certain populations and with obesity and metabolic syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014],

  • 细胞定位

    Nucleus . Cytoplasm . Cytoplasm, cytosol . Shuttling between the cytoplasm and the nucleus is under circadian regulation and is ARNTL/BMAL1-dependent. Phosphorylated form located in the nucleus while the nonphosphorylated form found only in the cytoplasm. Sequestered to the cytoplasm in the presence of ID2 (By similarity). Localizes to sites of DNA damage in a H2AX-independent manner. .