2022
DOI: 10.1016/j.xpro.2022.101336
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Live imaging of postembryonic developmental processes in C. elegans

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Cited by 2 publications
(2 citation statements)
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“…For detect the subcellular localization of DMA-1 in different mutations, hermaphrodite animals were anesthetized using 5 mM levamisole in M9 buffer (Li et al, 2022; Wang et al, 2021), mounted on 2% agar pads and imaged using Zeiss Cell Observer SD spinning disk confocal microscope equipped with an alpha Plan-Apochromat 63x/1.46 NA objective. Fluorescence signals under excitation light at 488 nm and 561 nm were acquired, respectively (for the image shown in Figures 3A, 5D).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…For detect the subcellular localization of DMA-1 in different mutations, hermaphrodite animals were anesthetized using 5 mM levamisole in M9 buffer (Li et al, 2022; Wang et al, 2021), mounted on 2% agar pads and imaged using Zeiss Cell Observer SD spinning disk confocal microscope equipped with an alpha Plan-Apochromat 63x/1.46 NA objective. Fluorescence signals under excitation light at 488 nm and 561 nm were acquired, respectively (for the image shown in Figures 3A, 5D).…”
Section: Methodsmentioning
confidence: 99%
“…For detect the subcellular localization of DMA-1 in different mutations, hermaphrodite animals were anesthetized using 5 mM levamisole in M9 buffer (Li et al, 2022;Wang et al, 2021) 3B).…”
Section: Imagingmentioning
confidence: 99%