<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(zhì)保證 · 通蔚試劑

    當(dāng)前位置: 首頁 > 科研產(chǎn)品 > 科研抗體 > 其他抗體 > TRPC4AP 抗原(重組蛋白)

    產(chǎn)品中心

    最新產(chǎn)品

    • TRPC4AP 抗原(重組蛋白)

      規(guī)格:
      價(jià)格:
      • 品牌 : 通蔚生物
      • 目錄號(hào) : TW5808
      • 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)
    • 說明書下載
    • 商品評(píng)論0
    • 相關(guān)產(chǎn)品

    中文名稱: TRPC4AP 抗原(重組蛋白)

    英文名稱: TRPC4AP Antigen (Recombinant Protein)

    別     名 transient receptor potential cation channel, subfamily C, member 4 associated protein; TRUSS; TRRP4AP; PPP1R158; C20orf188

    儲(chǔ)     存: 冷凍(-20℃)

    相關(guān)類別:抗原

    概     述

    Fusion protein corresponding to C terminal 200 amino acids of human TRPC4AP

    技術(shù)規(guī)格

    Full name:

    transient receptor potential cation channel, subfamily C, member 4 associated protein

    Synonyms:

    TRUSS; TRRP4AP; PPP1R158; C20orf188

    Swissprot:

    Q8TEL6

    Gene Accession:

    BC013144

    Purity:

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

    Expression system:

    Escherichia coli

    Tags:

    His tag C-Terminus, GST tag N-Terminus

    Background:

    TRPC4AP (transient receptor potential cation channel, subfamily C, member 4 associated protein), also known as TRUSS or TRRP4AP, is a 797 amino acid protein that is expressed in a variety of tissues, with highest expression in liver, heart, testis and brain. Thought to function as a scaffolding protein, TRPC4AP interacts with TNF-R1 and may both link TNF-R1 to the IKK signalsome complex, and participate in the activation of NFκB p50, an event that occurs in response to TNF-R1 ligation. TRPC4AP exists as multiple alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.


    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>