<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(lái)到上海通蔚!

    021-54845833/15800441009

    品質(zhì)保證 · 通蔚試劑

    當(dāng)前位置: 首頁(yè) > 科研產(chǎn)品 > 科研抗體 > 其他抗體 > ZBTB20 抗原(重組蛋白)

    產(chǎn)品中心

    最新產(chǎn)品

    • ZBTB20 抗原(重組蛋白)

      規(guī)格:
      價(jià)格:
      • 品牌 : 通蔚生物
      • 目錄號(hào) : TW6616
      • 應(yīng)用 : 僅供科研使用
      • 貨期 : 現(xiàn)貨
      • 規(guī)格 :100ug
    • 商品詳情
    • 參考文獻(xiàn)
    • 說(shuō)明書下載
    • 商品評(píng)論0
    • 相關(guān)產(chǎn)品

    中文名稱: ZBTB20 抗原(重組蛋白)

    英文名稱: ZBTB20 Antigen (Recombinant Protein)

    別     名:
    zinc finger and BTB domain containing 20; HOF; DPZF; PRIMS; ODA-8S; ZNF288

    儲(chǔ)     存: 冷凍(-20℃)

    相關(guān)類別:抗原

    概     述

    Fusion protein corresponding to a region derived from 542-741 amino acids of human ZBTB20

    技術(shù)規(guī)格

    Full name:

    zinc finger and BTB domain containing 20

    Synonyms:

    HOF; DPZF; PRIMS; ODA-8S; ZNF288

    Swissprot:

    Q9HC78

    Gene Accession:

    BC029041

    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, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.


    產(chǎn)品掃碼查看詳情
    手機(jī)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>