金年会·(jinnianhui)金字招牌诚信至上-Gold Annual Meeting

<金年会·(jinnianhui)金字招牌诚信至上-Gold Annual Meetingj id='vfazma'>
<金年会·(jinnianhui)金字招牌诚信至上-Gold Annual Meeting id='jhgxdt'>
<金年会·(jinnianhui)金字招牌诚信至上-Gold Annual Meetingcdn class='yjzipk'>
    <金年会·(jinnianhui)金字招牌诚信至上-Gold Annual Meetingr class='melywg'>
  1. 欢迎来到上海金年会·(jinnianhui)金字招牌诚信至上-Gold Annual Meeting!

    021-54888888/15800441009

    品质保证 · 金年会·(jinnianhui)金字招牌诚信至上-Gold Annual Meeting试剂

    当前位置: 首页 > 科研产品 > 科研抗体 > 其他抗体 > FUNDC2抗原(重组蛋白)

    产品中心

    • FUNDC2抗原(重组蛋白)

      规格:
      数量:

      购买数量

      价格:
      • 品牌 : 金年会·(jinnianhui)金字招牌诚信至上-Gold Annual Meeting生物
      • 目录号 : TW18657
      • 应用 : 仅供科研使用
      • 保存条件 : 低温保存
      • 货期 : 现货
      • 商品库存:90
    • 商品详情
    • 参考文献
    • 说明书下载
    • 商品评论0
    • 相关产品

    中文名称:FUNDC2抗原(重组蛋白)

    英文名称: FUNDC2 Antigen (Recombinant Protein)

    别      名:DC44; HCC3; HCBP6; PD03104

    储      存: 冷冻(-20℃)

    相关类别: 抗原

    概      述:

    Fusion protein corresponding to a region derived from 1-189 amino acids of human FUNDC2


    技术规格:

    Full name:

    FUN14 domain containing 2

    Synonyms:

    DC44; HCC3; HCBP6; PD03104

    Swissprot:

    Q9BWH2

    Gene Accession:

    BC000255

    Purity:

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

    Expression system:

    Escherichia coli

    Tags:

    His tag C-Terminus, GST tag N-Terminus

    Background:

    FUNDC2 (FUN14 domain-containing protein 2), also known as HCC-3 (cervical cancer proto-oncogene 3 protein), HCBP6 (hepatitis C virus core-binding protein 6) or DC44, is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while 金年会·(jinnianhui)金字招牌诚信至上-Gold Annual Meetingo copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.


    【网站地图】【sitemap】
    【网站地图】【sitemap】