Immunofluorescence Detection of Callose in Plant Tissue Sections.

Callose Immunofluorescence microscopy Monoclonal antibody

Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2022
Historique:
entrez: 29 3 2022
pubmed: 30 3 2022
medline: 1 4 2022
Statut: ppublish

Résumé

The accumulation of the cell wall component callose at plasmodesmata (PD) is crucial for the regulation of symplastic intercellular transport in plants. Here we describe protocols to fluorescently image callose in sectioned plant tissue using monoclonal antibodies. This protocol achieves high-resolution images by the fixation, embedding, and sectioning of plant material to expose internal cell walls. By using this protocol in combination with high-resolution confocal microscopy, we can detect PD callose in a variety of plant tissues and species.

Identifiants

pubmed: 35349139
doi: 10.1007/978-1-0716-2132-5_10
doi:

Substances chimiques

Glucans 0
callose 9064-51-1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

167-176

Informations de copyright

© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Références

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doi: 10.1093/jxb/erx337
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doi: 10.1007/BF01280708
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doi: 10.4161/cib.26531
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Auteurs

Sam Amsbury (S)

School of Biosciences, The University of Sheffield, Sheffield, UK. s.amsbury@sheffield.ac.uk.

Yoselin Benitez-Alfonso (Y)

Centre for Plant Science, School of Biology, University of Leeds, Leeds, UK.

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Classifications MeSH