TPC2-A1-N
CAS No. 136186-07-7
TPC2-A1-N ( —— )
产品货号. M34883 CAS No. 136186-07-7
TPC2-A1-N 是一种强大的 Ca2+-可渗透双孔通道 2 (TPC2) 的激动剂,通过模拟 NAADP 的生理作用发挥作用。TPC2-A1-N 可诱导 TPC2 显著的 Ca2+ 响应 (EC50=7.8 μM),这种响应并可被一些 TPC 阻断剂阻断。TPC2-A1-N 可用于检测完整细胞中 TPC2 通道的不同功能。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥3256 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称TPC2-A1-N
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述TPC2-A1-N 是一种强大的 Ca2+-可渗透双孔通道 2 (TPC2) 的激动剂,通过模拟 NAADP 的生理作用发挥作用。TPC2-A1-N 可诱导 TPC2 显著的 Ca2+ 响应 (EC50=7.8 μM),这种响应并可被一些 TPC 阻断剂阻断。TPC2-A1-N 可用于检测完整细胞中 TPC2 通道的不同功能。
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产品描述TPC2-A1-N is a powerful and Ca2+-permeable agonist of?two pore?channel?2?(TPC2), which plays its role by mimicking the physiological actions?of?NAADP. TPC2-A1-P reproducibly?evokes significant Ca2+ responses from TPC2 (EC50=7.8 μM), and the effect can be blocked by several TPC blockers. TPC2-A1-N can be used to probe different functions of TPC2 channels in intact cells.
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体外实验Two-pore channels (TPC1-3) are ancient members of the voltage-gated ion channel superfamily. TPCs are expressed throughout the endo-lysosomal system and regulates the trafficking of various cargoes.TPC2 can mediate different physiological and possibly pathophysiological effects depending on how it is activated.?The?ion selectivity of TPC2 is not fixed but rather agonist-dependent. TPC2 is a unique example of an ion channel that conducts different ions in response to different activating ligands.TPC2-A1-N (10 μM) reproducibly evokes Ca2+?signals, and TPC2-A1-N response reachs its plateau faster than TPC2-A1-P. The EC50 in full concentration-effect relationships for the plateau response is 7.8 μM for TPC2-A1-N in a cell line stably expressing TPC2L11A/L12A.TPC2-A1-N (10 μM) evokes Ca2+?influx through the TPC2 pore evokes Ca2+?signals in cells expressing TPC2L11A/L12A?but not TPC2L11A/L12A/L265P. Additionally, the responses to TPC2-A1-N can be selectively blocked by the identified TPC2 blockers Tetrandrine (HY-13764, Tet), Raloxifene (HY-13738, Ral), and Fluphenazine (HY-A0081, Flu) by removal of extracellular Ca2+.In endo-lysosomal patch-clamp experiments, TPC2-A1-N (30 μM) elicits currents using Na+?as the major permeantion, in vacuolin-enlarged endo-lysosomes isolated from isolated from HEK293 cells transiently expressing human TPC2 (hTPC2) but not in cells expressing TPC1.In endo-lysosomal patch-clamp experiments, TPC2-A1-N (30 μM) induces larger currents in endo-lysosomes isolated from cells expressing a gain-of-function variant of TPC2 (TPC2M484L) compared to the wild-type isoform, and exhibits an EC50 value of 0.6 μM for TPC2-A1-N.
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体内实验——
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同义词——
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通路GPCR/G Protein
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靶点Calcium Channel
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受体Calcium Channel
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研究领域——
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适应症——
化学信息
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CAS Number136186-07-7
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分子量401.17
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分子式C17H9Cl2F3N2O2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 250 mg/mL (623.18 mM; 超声助溶 )
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SMILESO\C(=C(\C#N)C(=O)Nc1ccc(cc1)C(F)(F)F)c1cc(Cl)cc(Cl)c1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Susanne Gerndt, et al. Agonist-mediated switching of ion selectivity in TPC2 differentially promotes lysosomal function. Elife?
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