<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 > CCDC112 抗原(重組蛋白)

    產(chǎn)品中心

    最新產(chǎn)品

    • CCDC112 抗原(重組蛋白)

      規(guī)格:
      價格:
      • 品牌 : 通蔚生物
      • 目錄號 : TW4096
      • 應(yīng)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(xiàn)
    • 說明書下載
    • 商品評論0
    • 相關(guān)產(chǎn)品

    中文名稱: CCDC112 抗原(重組蛋白)

    英文名稱:CCDC112 Antigen (Recombinant Protein)

    別     名: coiled-coil domain containing 112; MBC1

    儲     存: 冷凍(-20℃)

    相關(guān)類別:抗原

    概     述

    Fusion protein corresponding to a region derived from 247-446 amino acids of human CCDC112

    技術(shù)規(guī)格

    Full name:

    coiled-coil domain containing 112

    Synonyms:

    MBC1

    Swissprot:

    Q8NEF3

    Gene Accession:

    BC031242

    Purity:

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

    Expression system:

    Escherichia coli

    Tags:

    His tag C-Terminus, GST tag N-Terminus

    Background:

    CCDC112 (coiled-coil domain containing 112), also known as MBC1 (mutated in bladder cancer 1), is a 446 amino acid protein. The gene encoding CCDC112 is located on chromosome 5. Due to alternative splicing events, CCDC112 exists as two isoforms. Chromosome 5 comprises about 6% of human genomic DNA and contains 181 million base pairs encoding around 1,000 genes. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic 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>