TRAP-6

Pricing Availability   Qty
说明: PAR1 peptide fragment (residues 42-47); acts as a PAR1 agonist
别名: Thrombin receptor activator peptide 6
纯度: ≥95% (HPLC)
说明书
引用文献 (8)
评论

生物活性 for TRAP-6

TRAP-6 is a peptide fragment (residues 42-47) of protease-activated receptor 1 (PAR1) that acts as a PAR1 agonist. Stimulates platelet aggregation (EC50 = 0.8 μM), promotes intracellular Ca2+ mobilization and induces rapid phosphodiesterase 3A (PDE3A) phosphorylation in vitro.

技术数据 for TRAP-6

分子量 748.88
公式 C34H56N10O9
序列 SFLLRN
储存 Store at -20°C
纯度 ≥95% (HPLC)
CAS Number 141136-83-6
PubChem ID 9831933
InChI Key HAGOWCONESKMDW-FRSCJGFNSA-N
Smiles [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(N)=O)C(O)=O

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for TRAP-6

溶解性 Soluble to 1 mg/ml in water

产品说明书 for TRAP-6

分析证书/产品说明书
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参考文献 for TRAP-6

参考文献是支持产品生物活性的出版物。

Vassallo et al (1992) Structure-function relationships in the activation of platelet thrombin receptors by receptor derived peptides. J.Biol.Chem. 267 6081 PMID: 1313429

Kaufmann et al (1999) PAR 1-type thrombin receptors are involved in thrombin-induced calcium signaling in human meningioma cells. J.Neurooncol. 42 131 PMID: 10421070

Hunter et al (2009) Protein kinase C-mediated phosphorylation and activation of PDE3A regulates cAMP levels in human platelets. J.Biol.Chem. 284 12339 PMID: 19261611


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关键词: TRAP-6, TRAP-6 supplier, PAR1, peptide, fragment, residues, 42-47, agonists, Receptors, Protease-Activated, proteinase-activated, Thrombin, receptor, activator, peptide6, 6, 3497, Tocris Bioscience

8 篇 TRAP-6 的引用文献

引用文献是使用了 Tocris 产品的出版物。 TRAP-6 的部分引用包括:

Elenbaas et al (2023) SVEP1 is an endogenous ligand for the orphan receptor PEAR1 Nat Commun 14 850 PMID: 36792666

Dhenge et al (2017) Arachidonic acid and Docosahexanoic acid enhance platelet formation from human apheresis-derived CD34+ cells. Cell Cycle 16 979 PMID: 28388313

Angelo et al (2021) PAR-4/Ca2+-calpain pathway activation stimulates platelet-derived microparticles in hyperglycemic type 2 diabetes. Cardiovasc Diabetol 20 77 PMID: 33812377

Gockel et al (2018) The Low Molecular Weight HP Tinzaparin Attenuates Platelet Activation in Terms of Metastatic Niche Formation by Coagulation-Dependent and Independent Pathways. Molecules 23 PMID: 30356007


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