发布: 2015年05月05日第5卷第9期 DOI: 10.21769/BioProtoc.1462 浏览次数: 10764
评审: Maria SinetovaAlexander JonesAnonymous reviewer(s)
Abstract
Cytoplasmic calcium ([Ca2+]cyt) acts as a stimulus-induced second messenger in multiple signal transduction cascades (Allen et al., 1999). In plant cells, a dramatic and readily assayed response to stimulus is the change of stomatal aperture. Changes in [Ca2+]cyt of stomatal guard cells were involved in stomatal movement in response to various stimuli and cellular processes. In general, there are two available ways to measure [Ca2+]cyt in guard cells, i.e., loading of calcium-sensitive fluorescence dyes such as fluo-3 AM and fura-2 or expressing genetically encoded calcium indicators such as yellow cameleon (Krebs et al., 2012). In this protocol, we aim at describing the experimental procedure to record [Ca2+]cyt fluctuation in guard cells with loading of fluo-3 AM upon ABA or PA treatment combining with fluorescence imaging performed with confocal laser scanning microscope.
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版权信息
© 2015 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Li, L., Lin, F., Qu, Y. and Zhang, Q. (2015). A Protocol to Measure the Cytoplasmic Calcium in Arabidopsis Guard Cells. Bio-protocol 5(9): e1462. DOI: 10.21769/BioProtoc.1462.
分类
植物科学 > 植物生理学 > 离子分析
生物化学 > 其它化合物 > 离子
细胞生物学 > 细胞成像 > 共聚焦显微镜
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