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Visualizing and Quantifying In Vivo Cortical Cytoskeleton Structure and Dynamics
A. Rosero, D. Oulehlová, V. Žárský, F. Cvrčková,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- Arabidopsis ultrastruktura MeSH
- cytoskelet ultrastruktura MeSH
- fluorescenční mikroskopie metody MeSH
- konfokální mikroskopie metody MeSH
- mikrotubuly ultrastruktura MeSH
- počítačové zpracování obrazu metody MeSH
- rostlinné buňky ultrastruktura MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
The cortical microtubule and actin meshworks play a central role in the shaping of plant cells. Transgenic plants expressing fluorescent protein markers specifically tagging the two main cytoskeletal systems are available, allowing noninvasive in vivo studies. Advanced microscopy techniques, in particular confocal laser scanning microscopy (CLSM), spinning disk confocal microscopy (SDCM), and variable angle epifluorescence microscopy (VAEM), can be nowadays used for imaging the cortical cytoskeleton of living cells with unprecedented spatial and temporal resolution. With the aid of free computing tools based on the publicly available ImageJ software package, quantitative information can be extracted from microscopic images and video sequences, providing insight into both architecture and dynamics of the cortical cytoskeleton.
Department of Experimental Plant Biology Faculty of Science Charles University Prague Czech Republic
Citace poskytuje Crossref.org
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- $a Rosero, Amparo $u Department of Experimental Plant Biology, Faculty of Science, Charles University, Prague, Czech Republic. Coordinación de Innovación Regional, C.I. Turipaná, Montería, Córdoba, Colombia.
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- $a The cortical microtubule and actin meshworks play a central role in the shaping of plant cells. Transgenic plants expressing fluorescent protein markers specifically tagging the two main cytoskeletal systems are available, allowing noninvasive in vivo studies. Advanced microscopy techniques, in particular confocal laser scanning microscopy (CLSM), spinning disk confocal microscopy (SDCM), and variable angle epifluorescence microscopy (VAEM), can be nowadays used for imaging the cortical cytoskeleton of living cells with unprecedented spatial and temporal resolution. With the aid of free computing tools based on the publicly available ImageJ software package, quantitative information can be extracted from microscopic images and video sequences, providing insight into both architecture and dynamics of the cortical cytoskeleton.
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- $a Oulehlová, Denisa $u Department of Experimental Plant Biology, Faculty of Science, Charles University, Prague, Czech Republic. Institute of Experimental Botany of the Czech Academy of Sciences, Prague, Czech Republic.
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