2020
DOI: 10.1007/978-1-0716-0672-8_8
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Workflow to Characterize Mutants with Reproductive Defects

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Cited by 4 publications
(2 citation statements)
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“…Pollinated pistils were incubated in the control or heat stress conditions for 12 hours. Pistils were excised and an aniline blue assay of pollinated pistils was performed as described 116 . Stained pistils were mounted and observed using epifluorescence microscopy on a Zeiss Axiovert 100 fluorescent microscope.…”
Section: Tomato Plant Growthmentioning
confidence: 99%
“…Pollinated pistils were incubated in the control or heat stress conditions for 12 hours. Pistils were excised and an aniline blue assay of pollinated pistils was performed as described 116 . Stained pistils were mounted and observed using epifluorescence microscopy on a Zeiss Axiovert 100 fluorescent microscope.…”
Section: Tomato Plant Growthmentioning
confidence: 99%
“…Investigating pollen tube growth through the pistil tissue would be an ideal way to study physical barriers associated with this process. Although various methodologies are used to realize this goal [27,28], this scenario imposes several critical limitations, including (1) asynchronous germination of pollen tubes, (2) crowding of pollen tubes within the pistil, (3) lack of control on the complex pistil biological system, and (4) the requirement for advanced imaging methods to visualize pollen tubes in living pistils. To circumvent some of these challenges, microfluidic platforms have been exploited to provide defined microenvironments for single-cell analysis of pollen tubes and address key biophysical questions about their behavior during the process of pistil penetration.…”
Section: Pollen Tube Behavior During Encounters With Inanimate Barriersmentioning
confidence: 99%