PeproTech重组人sIL-6 Receptor α (CHO cell derived) 1000ug-细胞/细菌培养-试剂-生物在线
PeproTech重组人sIL-6 Receptor α (CHO cell derived) 1000ug

PeproTech重组人sIL-6 Receptor α (CHO cell derived) 1000ug

商家询价

产品名称: PeproTech重组人sIL-6 Receptor α (CHO cell derived) 1000ug

英文名称: Human sIL-6 Receptor α (CHO cell derived)

产品编号: 200-06RC

产品价格: 0

产品产地: 美国

品牌商标: PeproTech/派普泰克

更新时间: null

使用范围: null

美国PeproTech(派普泰克)公司中国代表处
  • 联系人 :
  • 地址 :  江苏省苏州市工业园区星湖街218号A1北座4楼L03
  • 邮编 : 215123
  • 所在区域 : 江苏
  • 电话 :
  • 传真 : 0512-68325993
  • 邮箱 : peprotech.infochina@thermofisher.com

 

Recombinant Human sIL-6 Receptor α (CHO cell derived)

Catalog Number:
200-06RC
Synonyms:
soluble IL-6 receptor alpha, B cell stimulatory factor-2, CD126
Description:
IL-6 mediates its biological effects through the type I IL-6 receptor system that consists of two chains, IL-6Rα and gp130.  While the IL-6Rα chain is the binding component specific to IL-6, the gp130 chain only transmits signals of IL-6 when bound to IL-6Rα.  The gp130 can also transmit signals from LIF, OSM, CNTF, IL-11 and CT-1 in conjunction with other receptor subunits.  The low-affinity binding site for IL-6 is composed of IL-6Rα alone.  IL-6Rα is expressed in a wide range of cells, including T cells, fibroblasts and macrophages.  Soluble IL-6Rα, which consists of only the extracellular domain of the IL-6Rα chain, acts as an agonist of IL-6 activity at low concentrations. PeproTechs CHO cell-derived Recombinant Human sIL-6 Receptor α is a 37.9 kDa glycoprotein corresponding to 339 amino acid residues of the extracellular domain of IL-6Rα. As a result of glycosylation, Recombinant Human sIL-6 Receptor α migrates with an apparent molecular mass of approximately 57-70 kDa by SDS-PAGE gel, under reducing conditions.
AA Sequence:
LAPRRCPAQE VARGVLTSLP GDSVTLTCPG VEPEDNATVH WVLRKPAAGS HPSRWAGMGR RLLLRSVQLH DSGNYSCYRA GRPAGTVHLL VDVPPEEPQL SCFRKSPLSN VVCEWGPRST PSLTTKAVLL VRKFQNSPAE DFQEPCQYSQ ESQKFSCQLA VPEGDSSFYI VSMCVASSVG SKFSKTQTFQ GCGILQPDPP ANITVTAVAR NPRWLSVTWQ DPHSWNSSFY RLRFELRYRA ERSKTFTTWM VKDLQHHCVI HDAWSGLRHV VQLRAQEEFG QGEWSEWSPE AMGTPWTESR SPPAENEVST PMQALTTNKD DDNILFRDSA NATSLPVQD
Source:
CHO cells
Purity:
Greater than 95% by SDS-PAGE gel and HPLC analyses.
Biological Activity:
Determined by its ability to intensify the IL-6 induced growth inhibition of mouse M1 cells.  The expectedED50 is ≤ 5.0 ng/ml, in the presence of 20 ng/ml of rhIL-6.
 
 
 
 
Research Interests:
 
 
Country of Origin:
USA