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DC Field | Value | Language |
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dc.contributor.author | MATHEW, MABEL MARIA | en_US |
dc.contributor.author | SHANMUKHAN, ANJU | en_US |
dc.contributor.author | PALLIPURATH | en_US |
dc.contributor.author | VARAPPARAMBATH, VIJINA | en_US |
dc.contributor.author | PRASAD, KALIKA | en_US |
dc.date.accessioned | 2024-04-24T05:42:25Z | - |
dc.date.available | 2024-04-24T05:42:25Z | - |
dc.date.issued | 2023-06 | en_US |
dc.identifier.citation | Star Protocol, 4(02), 102184. | en_US |
dc.identifier.issn | 2666-1667 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.xpro.2023.102184 | en_US |
dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8664 | - |
dc.description.abstract | Here, we provide a protocol for real-time tracking of regenerating shoot progenitors, combined with polar protein quantification and targeted laser ablation of callus cells in Arabidopsis. Using Arabidopsis strains expressing GFP-labeled polar auxin efflux carrier, PINFORMED 1 (PIN1) protein, we detail steps to prepare the callus for time-lapse confocal imaging and track the progenitors expressing PIN1-GFP, followed by mapping and quantifying PIN1 polarity using Fiji/ImageJ. We then describe targeted laser ablation of cells and subsequent time-lapse imaging to study regeneration. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier B.V. | en_US |
dc.subject | Cell Biology | en_US |
dc.subject | Developmental biology | en_US |
dc.subject | Microscopy | en_US |
dc.subject | Plant sciences | en_US |
dc.subject | 2023 | en_US |
dc.title | Protocol for real-time imaging, polar protein quantification, and targeted laser ablation of regenerating shoot progenitors in Arabidopsis | en_US |
dc.type | Article | en_US |
dc.contributor.department | Dept. of Biology | en_US |
dc.identifier.sourcetitle | Star Protocol | en_US |
dc.publication.originofpublisher | Foreign | en_US |
Appears in Collections: | JOURNAL ARTICLES |
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