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SKOR1 Antibody, HRP conjugated

  • 中文名稱:
    SKOR1兔多克隆抗體, HRP偶聯
  • 貨號:
    CSB-PA308064HB01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) SKOR1 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    SKOR1
  • 別名:
    SKOR1 antibody; CORL1 antibody; FUSSEL15 antibody; LBXCOR1 antibody; SKI family transcriptional corepressor 1 antibody; Functional Smad-suppressing element on chromosome 15 antibody; Fussel-15 antibody; LBX1 corepressor 1 antibody; Ladybird homeobox corepressor 1 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human SKI family transcriptional corepressor 1 protein (744-965AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    HRP
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA
  • Protocols:
  • 儲存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期:
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
  • 用途:
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 功能:
    Acts as a transcriptional corepressor of LBX1. Inhibits BMP signaling.
  • 基因功能參考文獻:
    1. Permanent expression of Fussel-15 in keloid and skin sclerosis fibroblasts could be involved in the pathogenesis of these conditions. PMID: 21641385
    2. a novel gene, fussel-15 (functional smad suppressing element on chromosome 15) with high homology to the recently discovered Fussel-18 protein. PMID: 17292623
    3. MEIS1 and LBXCOR1 are developmental factors and raise new pathophysiologic questions for RLS. PMID: 18541116
    4. Observational study of gene-disease association. (HuGE Navigator) PMID: 19822783
    5. Observational study of gene-disease association. (HuGE Navigator) PMID: 19279021
    6. Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) PMID: 17637780

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  • 亞細胞定位:
    Nucleus.
  • 蛋白家族:
    SKI family
  • 組織特異性:
    Present specifically in cerebellar Purkinje cells (at protein level).
  • 數據庫鏈接:

    HGNC: 21326

    OMIM: 611273

    KEGG: hsa:390598

    STRING: 9606.ENSP00000369374

    UniGene: Hs.451224



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