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UTPγS trisodium salt
Selective P2Y2 and P2Y4 receptor agonist. Enzymatically stable.
|Storage||Desiccate at -20°C|
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
|Solvent||Max Conc. mg/mL||Max Conc. mM|
Preparing Stock Solutions
The following data is based on the product molecular weight 566.15. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
|Concentration / Solvent Volume / Mass||1 mg||5 mg||10 mg|
|1 mM||1.77 mL||8.83 mL||17.66 mL|
|5 mM||0.35 mL||1.77 mL||3.53 mL|
|10 mM||0.18 mL||0.88 mL||1.77 mL|
|50 mM||0.04 mL||0.18 mL||0.35 mL|
References are publications that support the biological activity of the product.
Lazarowski et al (1996) Enzymatic synthesis of UTPγS, a potent hydrolysis resistant agonist of P2U-purinoceptors. Br.J.Pharmacol. 117 203 PMID: 8825364
Malmsjo et al (2000) The stable pyrimidines UDPβS and UTPγS discriminate between the P2 receptors that mediate vascular contraction and relaxation of the rat mesenteric artery. Br.J.Pharmacol. 131 51 PMID: 10960068
Malmsjo et al (2003) The stable pyrimidines UDPβS and UTPγS discriminate between contractile cerebrovascular P2 receptors. Eur.J.Pharmacol. 458 305 PMID: 12504787
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Keywords: UTPgS trisodium salt, UTPgS trisodium salt supplier, Selective, P2Y2/4, agonists, Receptors, Purinergic, purinoceptors, UTPgammaS, UTPγS, trisodium, salt, P2Y, 3279, Tocris Bioscience
1 Citation for UTPγS trisodium salt
Citations are publications that use Tocris products. Selected citations for UTPγS trisodium salt include:
Gault et al (2014) Osmotic surveillance mediates rapid wound closure through nucleotide release. J Cell Biol 207 767 PMID: 25533845
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