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Protease-Activated Receptor-1, PAR-1 Agonist 1, amide - 5 mg
- Cat.Number : AS-62937
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Protease activated receptor 1 (PAR-1) belongs to a subfamily of G-protein coupled receptors and is known to mediate the cellular effects of thrombin. This peptide is a PAR-1 selective agonist displaying a high level of specificity to PAR-1 over PAR-2. The specificity of peptide was evaluated in cell-based calcium signaling assay using HEK293 cells. PAR-1 selective agonists can be used to study PAR-1 activation in vivo. In addition to its varied cellular effects of thrombin, PAR-1 has also been shown to coordinate with PAR-4 and regulate thrombin-induced hepatocellular carcinoma harboring thrombin formation within the tumor environment classified as 'coagulation type'.
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Citations
Protease-activated receptor-2 activation induces acute lung inflammation by neuropeptide-dependent mechanisms 1
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- X. Su
- et al
Chronic exposure to fibrin and fibrinogen differentially regulates intracellular Ca2+ in human pulmonary arterial smooth muscle and endothelial cells.
Am J Physiol Lung Cell Mol Physiol. . 2009 Apr 10 ; 296(6) L979 | DOI : 10.1152/ajplung.90412.2008
- AL. Firth
- et al
Thrombin- and Factor Xa–induced DNA synthesis is mediated by transactivation of fibroblast growth factor receptor-1 in human vascular smooth muscle cells.
Circ. Res . 2003 Dec 11 ; 94(3) 340 | DOI : 10.1161/01.RES.0000111805.09592.D8
- BH. Rauch
- et al
Kallikrein-related peptidase-4 initiates tumor-stroma interactions in prostate cancer through protease-activated receptor-1
Int J Cancer. . 2010 Feb 01 ; 126(3) 599 | DOI : 10.1002/ijc.24904
- W. Wang
- et al
Prostate-specific kallikreins-2 and -4 enhance the proliferation of DU-145 prostate cancer cells through protease-activated receptors-1 and -2.
Mol Cancer Res. . 2008 Jun 01 ; 6(6) 1D46 | DOI : 10.1158/1541-7786.MCR-08-0096
- G. Mize
- et al
Transcription of Interleukin-25 and extracellular release of the protein is regulated by allergen proteases in airway epithelial cells
Am J Respir Cell Mol Biol. . 2013 Nov 01 ; 49(5) 741 | DOI : 10.1165/rcmb.2012-0304OC
- H. Kouzaki
- et al