FoxP2 Rabbit mAb

活动价:

¥880.00

市场价:¥1280.00

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产品规格:
  • 50μL
货号:

FAB2622234

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商品描述
  • 靶点-Target

    FoxP2

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB,IF,IP,ELISA

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG,Kappa

  • 修饰-Modification

    Unmodified

  • MW(Calculated)

    80kD

  • MW(Observed)

    95kD

  • 推荐稀释比

    WB 1:1000-1:5000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;

  • 组成

    PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA

  • 纯化工艺

    Protein A

  • 储存

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

  • 克隆号

    Monoclonal

  • 免疫原

    PT1405R

  • 特异性

    Endogenous

  • 基因名称

    FOXP2

  • 蛋白名称

    Forkhead box protein P2

  • 别名

    FOXP2;CAGH44;TNRC10;Forkhead box protein P2;CAG repeat protein 44;Trinucleotide repeat-containing gene 10 protein

  • Organism-1

    Human

  • 基因ID-1

    93986

  • SwissProt-1

    O15409

  • Organism-2

    Mouse

  • SwissProt-2

    P58463

  • 背景

    This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isofor

  • 细胞定位

    Nucleus .