多肽定制PAR-2 (1-6)) amide (human)) (scrambled) 编码

上海金畔生物科技有限公司可以定制不同序列多肽,可以访问官网了解更多产品信息。

名称 PAR-2 (1-6)) amide (human)) (scrambled)
编码
别名 PAR-2 (1-6)) amide (human)) (scrambled)
纯度 80%,90%,95%,98%,99%
重量 1mg,5mg,10mg,50mg,100mg,1g
序列(单字母缩写) LSIGKV-NH2
序列(三字母缩写) H-Leu-Ser-Ile-Gly-Lys-Val-NH2?(trifluoroacetate salt)
基本描述 The peptide T1 is the thrombin receptor domain, which functions as a tethered ligand for the receptor itself. T1 is an inhibitor of thrombin triggered platelet aggregation, serotonin release and tyrosine phosphorylation. Its anti-aggregatory activity was about ten-fold higher than that of the previously reported peptide antagonists of the thrombin receptor. This peptide has served as model peptide in protein modification and MS studies.
溶解度
分子量 614.79
化学式 C28H54N8O7
存储条件 Store at -20°C. Keep tightly closed. Store in a cool dry place.
注释
Documents PAR-2 (1-6))  amide (human))  (scrambled)          编码
Figures PAR-2 (1-6))  amide (human))  (scrambled)          编码
Reference H.Nishikawa et al., J. Pharmacol. Exp. Ther., 312, 324 (2005) I.A. Akers et al.,Am. J. Physiol. Lung Cell. Mol. Physiol., 278, L193 (2000) S. Miyata, et al., J. Biol. Chem., 275, 4592 (2000) S. Miike, A.S. McWilliam, and H. Kita, J. Immunol., 167, 6615 (2001)
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多肽定制Scrambled TRAP Fragment 编码 [374898-11-0]

上海金畔生物科技有限公司可以定制不同序列多肽,可以访问官网了解更多产品信息。

名称 Scrambled TRAP Fragment
编码 [374898-11-0]
别名 Scrambled TRAP Fragment
纯度 80%,90%,95%,98%,99%
重量 1mg,5mg,10mg,50mg,100mg,1g
序列(单字母缩写) FSLLRN-NH2
序列(三字母缩写) H-Phe-Ser-Leu-Leu-Arg-Asn-NH2?(trifluoroacetate salt)
基本描述 This is a peptide analogue of thrombin receptor activating peptide. It is been shown to block alpha-thrombin and thrombin receptor activating peptide-induced platelet aggregation in vitro and inhibit thrombosis in in vivo animal models.
溶解度
分子量 747.89
化学式 C34H57N11O8
存储条件 Store at -20°C. Keep tightly closed. Store in a cool dry place.
注释
Documents Scrambled TRAP Fragment          编码     [374898-11-0]
Figures Scrambled TRAP Fragment          编码     [374898-11-0]
Reference Ahn, HS. et al. Mol. Pharmacol. 51, 350 (1997)
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