<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(yè) > 科研產(chǎn)品 > 科研抗體 > 其他抗體 > FSD1L 抗原(重組蛋白)

    產(chǎn)品中心

    最新產(chǎn)品

    • FSD1L 抗原(重組蛋白)

      規(guī)格:
      價(jià)格:
      • 品牌 : 通蔚生物
      • 目錄號(hào) : TW11065
      • 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: FSD1L 抗原(重組蛋白)

    英文名稱: FSD1L Antigen (Recombinant Protein)

    別      名:fibronectin type III and SPRY domain containing 1-like; MIR1; CCDC10; FSD1CL; FSD1NL; CSDUFD1

    儲(chǔ)      存:冷凍(-20℃)

    相關(guān)類別:抗原

    概述

    Fusion protein corresponding to a region derived from 331-530 amino acids of human FSD1L


    技術(shù)規(guī)格

    Full name:

    fibronectin type III and SPRY domain containing 1-like

    Synonyms:

    MIR1; CCDC10; FSD1CL; FSD1NL; CSDUFD1

    Swissprot:

    Q9BXM9

    Gene Accession:

    BC036746

    Purity:

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

    Expression system:

    Escherichia coli

    Tags:

    His tag C-Terminus, GST tag N-Terminus

    Background:

    FSD1L (fibronectin type III and SPRY domain containing 1-like), also known as CCDC10 (coiled-coil domain-containing protein 10), CSDUFD1, MIR1 or FSD1CL, is a 530 amino acid protein containing one B30.2/SPRY domain, one COS domain, and a fibronectin type-III domain. Existing as three alternatively spliced isoforms, FSD1L is expressed primarily in brain, with lower levels of expression found in thymus, pituitary and testis. FSD1L may function in microtubule binding during interphase and is encoded by a gene that maps to human chromosome 9q31.2. Chromosome 9 consists of about 145 million bases andd comprises approximately 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype.


    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>