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Submit ReviewNAADP tetrasodium salt is a Ca2+ mobilizing agent. Initiates Ca2+ release via type 1 ryanodine receptor (RyR1) activation. Also regulates Ca2+ release from intracellular stores distinct from the endoplasmic reticulum (ER); displays affinity for two-pore channels (TPCs) which release Ca2+ from acidic organelles.
分子量 | 832.32 |
公式 | C21H23N6Na4O18P3 |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
PubChem ID | 90488897 |
InChI Key | NWKIGVGTZIAOCW-MCNGMCCKSA-J |
Smiles | [Na+].[Na+].[Na+].[Na+].NC1=C2N=CN([C@@H]3O[C@H](COP([O-])(=O)OP([O-])(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)[N+]4=CC(=CC=C4)C([O-])=O)[C@@H](O)[C@H]3OP([O-])([O-])=O)C2=NC=N1 |
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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
water | 41.62 | 50 |
以下数据基于产品分子量 832.32。 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.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.5 mM | 2.4 mL | 12.01 mL | 24.03 mL |
2.5 mM | 0.48 mL | 2.4 mL | 4.81 mL |
5 mM | 0.24 mL | 1.2 mL | 2.4 mL |
25 mM | 0.05 mL | 0.24 mL | 0.48 mL |
参考文献是支持产品生物活性的出版物。
Calcraft et al (2009) NAADP mobilizes calcium from acidic organelles through two-pore channels. Nature 459 596 PMID: 19387438
Dammerman et al (2009) NAADP-mediated Ca2+ signaling via type 1 ryanodine receptor in T cells revealed by a synthetic NAADP agonist. Proc.Natl.Acad.Sci. 106 10678
Galion (2006) NAADP, a new intracellular messenger that mobilizes Ca2+ from acidic stores. Biochem.Soc.Transactions 34 922
If you know of a relevant reference for NAADP tetrasodium salt, please let us know.
关键词: NAADP tetrasodium salt, NAADP tetrasodium salt supplier, general, Calcium, Signaling, Signalling, Agents, Ca2+, mobilization, beta-NAADP, β-NAADP, ryanodine, receptors, 5502-96-5, General, Ryanodine, Receptors, 3905, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 NAADP tetrasodium salt 的部分引用包括:
Wang et al (2012) TPC proteins are phosphoinositide- activated sodium-selective ion channels in endosomes and lysosomes. Cell 151 372 PMID: 23063126
Olimpia et al (2023) Mu opioid receptor-mediated release of endolysosome iron increases levels of mitochondrial iron, reactive oxygen species, and cell death. NeuroImmune Pharm Ther 2 19-35 PMID: 37027339
Nicole et al (2020) Agonist-mediated switching of ion selectivity in TPC2 differentially promotes lysosomal function. Elife 9 PMID: 32167471
Ruas et al (2015) Expression of Ca2+-permeable two-pore channels rescues NAADP signalling in TPC-deficient cells. Am J Physiol Gastrointest Liver Physiol NULL PMID: 25872774
Hadi et al (2018) Macrophage-derived netrin-1 promotes abdominal aortic aneurysm formation by activating MMP3 in vascular smooth muscle cells. Nat Commun 9 5022 PMID: 30479344
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