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- 详细信息
- 文献和实验
- 技术资料
- 库存:
355
- 英文名:
Sodium Channel inhibitor 1
- CAS号:
1198117-23-5
- 保质期:
2年
- 供应商:
北京百奥莱博科技有限公司
- 保存条件:
-20℃,有效期2年,溶入溶剂后-20℃
- 规格:
1mL(10mM)|2mg|5mg|10mg|50mg|100mg
特别提示:包括Sodium Channel inhibitor 1在内,本公司的所有产品仅可用于科研实验,严禁用于临床医疗及其他非科研用途!
产品名称:Sodium Channel inhibitor 1
英文名称:Sodium Channel inhibitor 1
CAS#:1198117-23-5
产品货号:M06200
产品规格:1mL(10mM)|2mg|5mg|10mg|50mg|100mg
Sodium Channel inhibitor1是新型的选择性电压门控钠离子通道,可用于疼痛治疗。
注:本品仅可用于科研实验,严禁用于临床医疗及其他用途!
CAS号:1198117-23-5
分子式:C₂₄H₁₉F₄N₃O₃
分子量:473.42
结构式:
储存条件:-20℃,有效期2年,溶入溶剂后-20℃请尽量在一个月内使用。
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文献和实验CFTR Regulation of Epithelial Sodium Channel
channel belonging to the ABC (A TP B inding C assette) superfamily of transporters. The members of this superfamily use ATP hydrolysis to fulfill their function as active transporters. So far, CFTR is the only member of this family to function as a cAMP
Epithelial Sodium Channel in Planar Lipid Bilayers
Amiloride-sensitive Na+ channels belong to the epithelial Na+ channel (ENaC)-degenerin superfamily of ion channels. In addition to their key role in sodium handling, they serve diverse functions in many tissues. Improper functioning of ENaC
The amiloride-sensitive epithelial Na+ channel (ENaC) is typically composed of three structurally related subunits termed α, β, and γ. We describe methods to determine the functional subunit stoichiometry of ENaC based on a biophysical
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