<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 > CNTNAP2 抗原(重組蛋白)

    產品中心

    • CNTNAP2 抗原(重組蛋白)

      規(guī)格:
      價格:
      • 品牌 : 通蔚生物
      • 目錄號 : TW4325
      • 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: CNTNAP2 抗原(重組蛋白)

    英文名稱:CNTNAP2 Antigen (Recombinant Protein)

    別     名: contactin associated protein-like 2; CDFE; NRXN4; AUTS15; CASPR2; PTHSL1

    儲    存: 冷凍(-20℃)

    相關類別:抗原

    概     述

    Fusion protein corresponding to a region derived from 1132-1331 amino acids of human CNTNAP2

    技術規(guī)格

    Full name:

    contactin associated protein-like 2

    Synonyms:

    CDFE; NRXN4; AUTS15; CASPR2; PTHSL1

    Swissprot:

    Q9UHC6

    Gene Accession:

    BC113373

    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 a member of the neurexin family which functions in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains and a putative PDZ binding site. This protein is localized at the juxtaparanodes of myelinated axons, and mediates interactions between neurons and glia during nervous system development and is also involved in localization of potassium channels within differentiating axons. This gene encompasses almost 1.5% of chromosome 7 and is one of the largest genes in the human genome. It is directly bound and regulated by forkhead box protein P2 (FOXP2), a transcription factor related to speech and language development. This gene has been implicated in multiple neurodevelopmental disorders, including Gilles de la Tourette syndrome, schizophrenia, epilepsy, autism, ADHD and mental retardation.


    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>