Pregled bibliografske jedinice broj: 125962
Confocal fluorescence microscopy of the plant cytoskeleton
Confocal fluorescence microscopy of the plant cytoskeleton // Periodicum biologorum, 105 (2003), 3; 237-249 (međunarodna recenzija, članak, znanstveni)
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Naslov
Confocal fluorescence microscopy of the plant cytoskeleton
Autori
Weber, Igor
Izvornik
Periodicum biologorum (0031-5362) 105
(2003), 3;
237-249
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
microtubules; microfilaments; actin; tubulin; cytokinesis; cell growth
Sažetak
Confocal laser scanning microscopy has become a widespread method for examination of the supramolecular structure in fluorescently labeled cells. Its ability to substantially reduce out-of-focus blur provides a significant improvement in resolution along the optical axis of a microscope and enables optical sectioning of thick specimens. These features are particularly helpful for investigation of plant cells and tissues, which have been difficult to analyze at high resolution by traditional microscopy because of their shape, size, and optical properties. I will review the contributions that confocal microscopy has made to the study of the plant cytoskeleton. The operational principle of confocal microscopy will be introduced, including a discussion of recent technical advances relevant for investigation of plant cells. A number of representative studies of both fixed and live plant cells will be referred to, in which confocal microscopy has provided new and much clearer information about cytoskeletal structure than has been possible to obtain with conventional wide-field fluorescence microscopy. Finally, special attention will be given to visualization of microtubules and actin microfilaments in growth and division of plant cells.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
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