<ul id="eack0"><dfn id="eack0"></dfn></ul>
  • <strike id="eack0"><menu id="eack0"></menu></strike>
  • <strike id="eack0"><input id="eack0"></input></strike>
    
    
  • <strike id="eack0"><menu id="eack0"></menu></strike>
  • <strike id="eack0"><menu id="eack0"></menu></strike>
  • <strike id="eack0"></strike>
    歡迎來到上海通蔚!

    021-54845833/15800441009

    品質保證 · 通蔚試劑

    當前位置: 首頁 > 科研產品 > 科研抗體 > 其他抗體 > NIPBL抗原(重組蛋白)

    產品中心

    • NIPBL抗原(重組蛋白)

      規(guī)格:
      價格:
      • 品牌 : 通蔚生物
      • 目錄號 : TW18310
      • 應用 : 僅供科研使用
      • 貨期 : 現(xiàn)貨
      • 規(guī)格 :1mg/100ug
    • 商品詳情
    • 參考文獻
    • 說明書下載
    • 商品評論0
    • 相關產品

    中文名稱:NIPBL抗原(重組蛋白)

    英文名稱: NIPBL Antigen (Recombinant Protein)

    別      名: CDLS; IDN3; Scc2; CDLS1; IDN3-B

    儲      存: 冷凍(-20℃)

    相關類別: 抗原

    概      述:

    Fusion protein corresponding to a region derived from 2523-2687 amino acids of human NIPBL


    技術規(guī)格:

    Full name:

    NIPBL, cohesin loading factor

    Synonyms:

    CDLS; IDN3; Scc2; CDLS1; IDN3-B

    Swissprot:

    Q6KC79

    Gene Accession:

    BC033847

    Purity:

    >85%, as determined by Coomassie blue stained SDS-PAGE

    Expression system:

    Escherichia coli

    Tags:

    His tag C-Terminus, GST tag N-Terminus

    Background:

    This gene encodes the homolog of the Drosophila melanogaster Nipped-B gene product and fungal Scc2-type sister chromatid cohesion proteins. The Drosophila protein facilitates enhancer-promoter communication of remote enhancers and plays a role in developmental regulation. It is also homologous to a family of chromosomal adherins with broad roles in sister chromatid cohesion, chromosome condensation, and DNA repair. The human protein has a bipartite nuclear targeting sequence and a putative HEAT repeat. Condensins, cohesins and other complexes with chromosome-related functions also contain HEAT repeats. Mutations in this gene result in Cornelia de Lange syndrome, a disorder characterized by dysmorphic facial features, growth delay, limb reduction defects, and cognitive disability. Two transcript variants encoding different isoforms have been found for this gene.


    產品掃碼查看詳情
    手機掃描查看
    <ul id="eack0"><dfn id="eack0"></dfn></ul>
  • <strike id="eack0"><menu id="eack0"></menu></strike>
  • <strike id="eack0"><input id="eack0"></input></strike>
    
    
  • <strike id="eack0"><menu id="eack0"></menu></strike>
  • <strike id="eack0"><menu id="eack0"></menu></strike>
  • <strike id="eack0"></strike>