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Protocol for culturing and imaging of ectodermal cells from Xenopus
The Xenopus embryo provides an advantageous model system where genes can be readily transplanted as DNA or mRNA or depleted with antisense techniques. Here, we present a protocol to culture and image the cell biological properties of explanted Xenopus cap cells in tissue culture. We illustrate how t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293668/ https://www.ncbi.nlm.nih.gov/pubmed/35839770 http://dx.doi.org/10.1016/j.xpro.2022.101455 |
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author | Tejeda-Muñoz, Nydia Monka, Julia De Robertis, Edward M. |
author_facet | Tejeda-Muñoz, Nydia Monka, Julia De Robertis, Edward M. |
author_sort | Tejeda-Muñoz, Nydia |
collection | PubMed |
description | The Xenopus embryo provides an advantageous model system where genes can be readily transplanted as DNA or mRNA or depleted with antisense techniques. Here, we present a protocol to culture and image the cell biological properties of explanted Xenopus cap cells in tissue culture. We illustrate how this protocol can be applied to visualize lysosomes, macropinocytosis, focal adhesions, Wnt signaling, and cell migration. For complete details on the use and execution of this protocol, please refer to Tejeda-Muñoz et al. (2022). |
format | Online Article Text |
id | pubmed-9293668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92936682022-07-20 Protocol for culturing and imaging of ectodermal cells from Xenopus Tejeda-Muñoz, Nydia Monka, Julia De Robertis, Edward M. STAR Protoc Protocol The Xenopus embryo provides an advantageous model system where genes can be readily transplanted as DNA or mRNA or depleted with antisense techniques. Here, we present a protocol to culture and image the cell biological properties of explanted Xenopus cap cells in tissue culture. We illustrate how this protocol can be applied to visualize lysosomes, macropinocytosis, focal adhesions, Wnt signaling, and cell migration. For complete details on the use and execution of this protocol, please refer to Tejeda-Muñoz et al. (2022). Elsevier 2022-07-14 /pmc/articles/PMC9293668/ /pubmed/35839770 http://dx.doi.org/10.1016/j.xpro.2022.101455 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Protocol Tejeda-Muñoz, Nydia Monka, Julia De Robertis, Edward M. Protocol for culturing and imaging of ectodermal cells from Xenopus |
title | Protocol for culturing and imaging of ectodermal cells from Xenopus |
title_full | Protocol for culturing and imaging of ectodermal cells from Xenopus |
title_fullStr | Protocol for culturing and imaging of ectodermal cells from Xenopus |
title_full_unstemmed | Protocol for culturing and imaging of ectodermal cells from Xenopus |
title_short | Protocol for culturing and imaging of ectodermal cells from Xenopus |
title_sort | protocol for culturing and imaging of ectodermal cells from xenopus |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293668/ https://www.ncbi.nlm.nih.gov/pubmed/35839770 http://dx.doi.org/10.1016/j.xpro.2022.101455 |
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