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Related Experiment Video

Updated: Jun 8, 2025

An Analytical Tool that Quantifies Cellular Morphology Changes from Three-dimensional Fluorescence Images
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Protocol to analyse the structural composition by fluorescence microscopy and different conventional and fluorescence

Agustín Maceda1, Agustina Rosa Andrés-Hernández2, Teresa Terrazas1

  • 1Universidad Nacional Autónoma de México, Instituto de Biología, Departamento de Botánica, Apdo. postal 70-367, 04510 Coyoacán, Cd. Mx., Mexico.

Methodsx
|November 1, 2024
PubMed
Summary

This study demonstrates safranin-fast green staining for plant cell wall anatomy using fluorescence microscopy. This permanent staining method effectively differentiates cell wall components for detailed analysis.

Keywords:
Acridine orangeCongo redEpifluorescenceImagejIntensity fluorescenceSafranin-fast green conventional staining with fluorescence microscopySafranin-fast green staining

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Area of Science:

  • Plant anatomy
  • Microscopy
  • Biochemistry

Background:

  • Safranin-fast green is a conventional stain for plant anatomical characterization.
  • Conventional fluorescence microscopy stains have limitations in differentiating plant cell wall components.
  • There is a need for reliable staining techniques for advanced plant cell wall analysis.

Purpose of the Study:

  • To describe a protocol for using safranin-fast green stain with fluorescence microscopy.
  • To evaluate the effectiveness of this technique for plant cell wall analysis.
  • To enable quantitative analysis of plant cell wall composition.

Main Methods:

  • Plant samples were stained with safranin-fast green.
  • Stained samples were analyzed using fluorescence microscopy.
  • Fluorescence intensity measurements were standardized for statistical analysis.

Main Results:

  • The safranin-fast green staining protocol is effective for fluorescence microscopy.
  • This method allows for permanent samples and clear differentiation of lignified and cellulosic walls.
  • The technique provides reliable data for statistical analysis of cell wall chemistry.

Conclusions:

  • Safranin-fast green staining is a valuable tool for plant cell wall fluorescence microscopy.
  • This protocol offers advantages over conventional fluorescence stains for anatomical studies.
  • The standardized measurements facilitate robust inference on plant cell wall chemical composition.