Abstract
Approaches for Ca(2+) measurement require data recording with high spatiotemporal resolution. This is achieved by combined usage of locally targeted genetically encoded calcium indicators (GECIs) and confocal laser scanning microscopy (CLSM). This protocol provides instructions for setting up a CLSM-based experiment to measure cytosolic and nuclear Ca(2+) dynamics in Arabidopsis lines expressing Yellow Cameleon Ca(2+) indicators.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Arabidopsis / cytology
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Calcium / analysis*
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Calcium-Binding Proteins / genetics
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Calcium-Binding Proteins / metabolism*
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Cations, Divalent / analysis
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Cell Nucleus / chemistry*
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Cytological Techniques / methods*
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Cytoplasm / chemistry*
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Fluorescent Dyes / metabolism*
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Microscopy, Confocal / methods*
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Plant Roots / cytology
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Staining and Labeling / methods
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Transgenes
Substances
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Calcium-Binding Proteins
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Cations, Divalent
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Fluorescent Dyes
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yellow cameleon
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Calcium