Catalog |
name |
Description |
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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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R-M-1103 |
PAR-3 (1-6) (human) trifluoroacetate salt,CAS:320347-28-2 |
The sequence TFRGAP mimicks the putative tethered ligand of human PAR-3 (protease activated receptor 3). |
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R-M-1108 |
Peptide Lv (rat) trifluoroacetate salt,CAS:1872441-58-1 |
Peptide Lv has been discovered via a computational bioinformatics-based screening process. The neuropeptide is expressed in retinal photoreceptor layer, hippocampus, olfactory bulb, cerebellum, cerebral cortex, lung, spleen, liver and intestine. Peptide Lv enhances L-type voltage-gated calcium channel (L-VGCC) currents in retinal photoreceptors. |
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