Advanced microscopy methods for bioimaging of mitotic microtubules in plants

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F18%3A73590438" target="_blank" >RIV/61989592:15310/18:73590438 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1016/bs.mcb.2018.03.019" target="_blank" >http://dx.doi.org/10.1016/bs.mcb.2018.03.019</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/bs.mcb.2018.03.019" target="_blank" >10.1016/bs.mcb.2018.03.019</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Advanced microscopy methods for bioimaging of mitotic microtubules in plants

Popis výsledku v původním jazyce

Mitotic cell division in plants is a dynamic process playing a key role in plantmorphogenesis, growth, and development. Since progress of mitosis is highly sensitive to external stresses, documentation of mitotic cell division in living plants requires fast and gentle live-cell imaging microscopy methods and suitable sample preparation procedures. This chapter describes, both theoretically and practically, currently used advanced microscopy methods for the live-cell visualization of the entire process of plant mitosis. These methods include microscopy modalities based on spinning disk, Airyscan confocal laser scanning, structured illumination, and light-sheet bioimaging of tissues or whole plant organs with diverse spatiotemporal resolution. Examples are provided from studies of mitotic cell division using microtubule molecular markers in the model plant Arabidopsis thaliana, and from deep imaging of mitotic microtubules in robust plant samples, such as legume crop species Medicago sativa.

Název v anglickém jazyce

Advanced microscopy methods for bioimaging of mitotic microtubules in plants

Popis výsledku anglicky

Mitotic cell division in plants is a dynamic process playing a key role in plantmorphogenesis, growth, and development. Since progress of mitosis is highly sensitive to external stresses, documentation of mitotic cell division in living plants requires fast and gentle live-cell imaging microscopy methods and suitable sample preparation procedures. This chapter describes, both theoretically and practically, currently used advanced microscopy methods for the live-cell visualization of the entire process of plant mitosis. These methods include microscopy modalities based on spinning disk, Airyscan confocal laser scanning, structured illumination, and light-sheet bioimaging of tissues or whole plant organs with diverse spatiotemporal resolution. Examples are provided from studies of mitotic cell division using microtubule molecular markers in the model plant Arabidopsis thaliana, and from deep imaging of mitotic microtubules in robust plant samples, such as legume crop species Medicago sativa.

Druh

C - Kapitola v odborné knize

CEP obor

—

OECD FORD obor

10601 - Cell biology

Projekt

<a href="/cs/project/LO1204" target="_blank" >LO1204: Udržitelný rozvoj výzkumu v Centru regionu Haná</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2018

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název knihy nebo sborníku

MITOSIS AND MEIOSIS, PART B

ISBN

978-0-12-814142-7

Počet stran výsledku

30

Strana od-do

129-158

Počet stran knihy

369

Název nakladatele

Elsevier Academic Press Inc.

Místo vydání

San Diego

Kód UT WoS kapitoly

000452410800008