Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8664
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dc.contributor.authorMATHEW, MABEL MARIAen_US
dc.contributor.authorSHANMUKHAN, ANJUen_US
dc.contributor.authorPALLIPURATHen_US
dc.contributor.authorVARAPPARAMBATH, VIJINAen_US
dc.contributor.authorPRASAD, KALIKAen_US
dc.date.accessioned2024-04-24T05:42:25Z-
dc.date.available2024-04-24T05:42:25Z-
dc.date.issued2023-06en_US
dc.identifier.citationStar Protocol, 4(02), 102184.en_US
dc.identifier.issn2666-1667en_US
dc.identifier.urihttps://doi.org/10.1016/j.xpro.2023.102184en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8664-
dc.description.abstractHere, 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.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectCell Biologyen_US
dc.subjectDevelopmental biologyen_US
dc.subjectMicroscopyen_US
dc.subjectPlant sciencesen_US
dc.subject2023en_US
dc.titleProtocol for real-time imaging, polar protein quantification, and targeted laser ablation of regenerating shoot progenitors in Arabidopsisen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleStar Protocolen_US
dc.publication.originofpublisherForeignen_US
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