欢迎来到上海通蔚!

021-54845833/15800441009

品质保证 · 通蔚试剂

当前位置: 首页 > 科研产品 > 科研抗体 > 其他抗体 > HSD17B13抗原(重组蛋白)

产品中心

  • HSD17B13抗原(重组蛋白)

    规格:
    数量:

    购买数量

    价格:
    • 品牌 : 通蔚生物
    • 目录号 : TW17434
    • 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:  HSD17B13抗原(重组蛋白)

英文名称: HSD17B13 Antigen (Recombinant Protein)

别      名: SCDR9; NIIL497; SDR16C3; HMFN0376

储      存: 冷冻(-20℃)

相关类别: 抗原

概  述:

Fusion protein corresponding to a region derived from 20-300 amino acids of human HSD17B13


技术规格:

Full name:

hydroxysteroid 17-beta dehydrogenase 13

Synonyms:

SCDR9; NIIL497; SDR16C3; HMFN0376

Swissprot:

Q7Z5P4

Gene Accession:

BC112303

Purity:

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

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

Hydroxysteroid (17-beta) dehydrogenase 13, also designated Short-chain dehydrogenase/reductase 9 (SCDR9), which regulate the availability of steroids within various tissues throughout the body. HSD17B13 is a 300 amino acid secreted protein that is highly expressed in liver and is also detected in ovary, bone marrow, kidney, brain, lung, skeletal muscle, bladder and testis. The gene encoding HSD17B13 maps to chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.