2-hr time-lapse imaging of A. thaliana leaf primordia

Published: 15 January 2024| Version 1 | DOI: 10.17632/mhd99xr6sz.1
Contributor:
Xin-Min Li

Description

Raw confocal stacks used for cell-cycle length measurement in the following study: TITLE: Cell-cycle-linked growth reprogramming encodes developmental time into leaf morphogenesis JOURNAL: Current Biology Article Type: Research Article Authors: Xin-Min Li, Hannah Jenke, Sören Strauss, Christos Bazakos, Gabriella Mosca, Rena Lymbouridou, Daniel Kierzkowski, Ulla Neumann, Purva Naik, Peter Huijser, Stefan Laurent, Richard S. Smith, Adam Runions, Miltos Tsiantis* *Corresponding Authors: Miltos Tsiantis (tsiantis@mpipz.mpg.de) Cellular growth of leaf primordia (genetic backgrounds and leaf nodes indicated) was monitored through live imaging at a high temporal resolution (2-hour time window). Plasma membranes (labeled with tdTomato fluorescence signals) were imaged using A Leica TCS SP8 Confocal Laser Scanning Microscope, and confocal images were channel-split and converted into .tif format stacks using FIJI. See the related publication for more details.

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Steps to reproduce

See the related publication for experimental details.

Institutions

Max-Planck-Institut fur Pflanzenzuchtungsforschung

Categories

Image Database, Cell Cycle in Plant Cell, Biological Development, Leaf Studies

Funding

Max Planck Society

Alexander von Humboldt Foundation

Federal Ministry of Education and Research

Deutsche Forschungsgemeinschaft

Licence