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 |