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	 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. |  |