- ¥2280 - 3280
- 钦诚
- QC-pk247mu02-r50ug
- 美国/中国
- 2025年07月13日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
避免反复冻融。2-8°C不超过一个月，-80°C不超过532个月
- 规格：
50ug/100ug
- 物种Mus musculus (Mouse，小鼠) 相同的名称，不同的物种。
- 来源原核表达
- 宿主E.coli
- 内毒素水平<1.0EU/µg(LAL法测定)
- 亚细胞定位n/a
- 预测分子量19.2kDa
- 实际分子量-(差异分析请参阅说明书)
- 片段与标签Ala161~Ile318 (Accession # Q8CI85) with N-terminal His Tag
- 缓冲液成份磷酸盐缓冲液（pH7.4，含有 0.01% SKL, 1mM DTT, 5% Trehalose和Proclin300.）
- 性状冻干粉
- 纯度> 95%
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文献和实验Measurement of Ca2+ Entry Using 45Ca2+
For decades, the measurement of extracellular Ca2+ (40 Cao 2+ ) entry into cells, using 45 Ca2+ as carrier, has been a widely used technique. One of the first studies was performed by Hodgkin and Keynes (1 ) to measure the rate at which 40
Neuronal Ca2+ signals occur in a very complex way. Direct imaging of Ca2+ changes in the soma, dendrites, and even single spines on fast time-scales greatly helps us understand the generation mechanism of diverse Ca
Glial cells are besides neurons the second major cell type of nervous systems and are either of neuroectodermal (macroglia) or mesodermal (microglia) origin. As electrically non-excitable cells, they employ calcium signals
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