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PAR-1 agonist peptide

*This product has been discontinued!*
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+.
RP19979
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Description

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+.

Sequence
{Ser}{Phe}{Leu}{Leu}{Arg}{Asn}
Sequence Shortening SFLLRN
Molecular Formula C34H56N10O9
Molecular Weight 748.87
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Purity 95%
Storage Store at -20°C.
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