|
服务
产品 
|
PAR-1 Agonist Peptide
| 名称
|
PAR-1 Agonist Peptide
|
| 别名
|
|
| 序列(单字母缩写)
|
SFLLRN
|
| 序列(三字母缩写)
|
{Ser}{Phe}{Leu}{Leu}{Arg}{Asn}
|
| 基本描述
|
This hexapeptide corresponding to residues 42-47 of the thrombin receptor has been shown to be a thrombin receptor activator. It caused half-maximal platelet aggregation at approx. 0.8 uM and was 5 times more potent than the parent peptide H-8105. In addition, SFLLRN is effective in causing tyrosine phosphorylation, inhibition of cAMP formation, and an increase in cytosolic Ca2+.
|
| 分子量
|
748.870
|
| 化学式
|
C34H56N10O9
|
| 纯度
|
> 95%
|
| 存储条件
|
Store at -20°C.
|
| 注释
|
|
| Documents
|
|
| Figures
|
|
| Reference
|
Simmons Sarah., et al. Thrombin induces release of proinflammatory chemokines interleukin-8 and interferon-c-induced protein-10 from cultured human fetal astrocytes. Neuroreport. 2013 Jan;24(1):36-40.
|
|