| Catalog | name | Description | price |
|---|---|---|---|
| R-M-1091 | Pancreatic Polypeptide (human) trifluoroacetate salt,CAS:75976-10-2 | As antagonist of CCK, PP inhibits pancreatic sedretion. PP also acts on the gastrointestinal motility, food intake, and metabolism. | price> |
| R-M-1094 | PAR-1 (1-6) (mouse, rat) trifluoroacetate salt,CAS:140436-67-5 | PAR-1 (1-6) (mouse, rat) trifluoroacetate salt,CAS:140436-67-5 is a PAR-1 agonist.It can be applied to the study of cardiovascular system & diseases and hematology. | price> |
| R-M-1095 | PAR-2 (1-6) (human) trifluoroacetate salt,CAS : 202933-49-1 | The PAR-2 agonist SLIGKV can be used for the investigation of receptor functions. | price> |
| R-M-1096 | PAR-2 (1-6) amide (human) trifluoroacetate salt,CAS:190383-13-2 | PAR-2 (1-6) amide (human) trifluoroacetate salt,CAS:190383-13-2 from ruixi.SLIGKV-amide, which corresponds to the tethered ligand sequence of human PAR-2 (protease activated receptor 2), can be used to investigate receptor functions. | price> |
| R-M-1097 | PAR-2 (6-1) amide (human) trifluoroacetate salt,CAS: 942413-05-0 | CAS: 942413-05-0,PAR-2 (6-1) amide (human) trifluoroacetate salt from ruixi.Retro-sequence of the proteinase-activated receptor-2 (PAR-2). VKGILS-amide is commonly used as an inactive control. | price> |
| R-M-1098 | PAR-2 (1-6) amide (human) (scrambled) trifluoroacetate salt,CAS:1348395-60-7 | LSIGKV-amide, a partially reversed human PAR-2 activating peptide serving as an inactive control for the PAR-2 agonist SLIGKV-amide. | price> |
| R-M-1099 | PAR-2 (1-6) amide (mouse, rat) trifluoroacetate salt,CAS:171436-38-7 | SLIGRL-amide, protease-activated receptor-2 (PAR2) selective agonist. The reverted PAR2 peptide can be used as inactive control. | price> |
| R-M-1100 | PAR-2 (1-6) (mouse, rat) trifluoroacetate salt,CAS : 164081-25-8 | Tethered ligand sequence of mouse PAR-2, which like the thrombin receptor is a protease-activated receptor present in keratinocytes. SLIGRL was found to be equipotent with SFLLRN in activating keratinocyte inositolphospholipid hydrolysis and calcium mobilization. | price> |
| R-M-1101 | (2-Furoyl)-PAR-2 (2-6)-Orn amide (mouse, rat) trifluoroacetate salt,CAS:729589-58-6 | (2-Furoyl)-PAR-2 (2-6)-Orn amide (mouse, rat) is a potent and selective PAR-2 agonist. In cultured human PAR-2-expressing cells (2-Furoyl)-LIGRLO-amide was equally effective as SLIGRL-amide, in rat PAR-2-expressing cells it was 10 to 25 times more potent than SLIGRLamide in increasing intracellular calcium levels. In bioassays of tissue PAR-2 activity, measured as arterial vasodilation and hyperpolarization this agonist was 10 to 300 times more potent than SLIGRLamide. | price> |
| R-M-1102 | PAR-2 (6-1) amide (mouse, rat) trifluoroacetate salt,CAS: 245329-01-5 | PAR-2 (6-1) amide (mouse, rat) trifluoroacetate salt,CAS: 245329-01-5 from ruixi.It is a synthetic peptide and can be used in the research of Hematology. | price> |

Items-$0.00

Email:
Tel.:
RuixiBiotechCo.Ltd /KamulinBiotechco.ltd
Add: Room 20F 2002, Meiyuan Building, Yanta District, Xi’ an City, Shaanxi Province 710061 China
Tel: 02988811435
Fax: (86-29)8881-1435
Email: sales@ruixibiotech.com
Web: http://www.ruixibiotech.com


