Related Experiment Video
Updated: Jan 30, 2026

Live Confocal Imaging of Developing Arabidopsis Flowers
Published on: April 1, 2017
A Simple Protocol for Imaging Floral Tissues of Arabidopsis with Confocal Microscopy
Andrea Gómez-Felipe1, Stefan de Folter2
1Unidad de Genómica Avanzada, Laboratorio Nacional de Genómica para la Biodiversidad (LANGEBIO), Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Irapuato, Guanajuato, Mexico.
Abstract:
We present a simple protocol to image floral tissues with confocal laser scanning microscopy (CLSM). Recently, new imaging techniques have emerged that improve the image quality of plant tissues. In this protocol, as an example, we focus on the fluorescence detection of the miRNA MIR164c precursor. Briefly, the method involves tissue clearing, cell wall staining, and the visualization of fluorescence in tissues in young floral buds of Arabidopsis with CLSM with the use of water dipping lenses.
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