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



    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 > EMC8抗原(重组蛋白)

    产品中心

    • EMC8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 : TW16574
      • 应用 : 仅供科研使用
      • 保存条件 : 低温保存
      • 货期 : 现货
      • 商品库存:60
    • 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: EMC8抗原(重组蛋白)

    英文名称: EMC8 Antigen (Recombinant Protein)

    储     存: 冷冻(-20℃)

    相关类别: 抗原

    概     述

    Full length fusion protein

    技术规格

    Full name:

    ER membrane protein complex subunit 8

    Synonyms:

    NOC4; COX4NB; C16orf2; C16orf4; FAM158B

    Swissprot:

    O43402

    Gene Accession:

    BC001472

    Purity:

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

    Expression system:

    Escherichia coli

    Tags:

    His tag C-Terminus, GST tag N-Terminus

    Background:

    COX4NB (Neighbor of COX4) is a 210 amino acid protein encoded by the human gene COX4NB. COX4NB belongs to the UPF0172 (NOC4) family and is found on chromosome 16, adjacent to the gene that encodes COX4. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene which encodes a critical CREB binding protein. Crohn’s disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other auto-immune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.



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