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Label free, quantitative single-cell fate tracking of time-lapse movies
Historically, the ability to perform multi-day time-lapse imaging of adherent cells required expensive and specialized microscopy equipment. As byproduct of this cost, many labs would synchronize cells using inhibitors such as hydroxyurea and thymidine, and or use fluorescent biosensors to minimize...
Autores principales: | Caldon, C. Elizabeth, Burgess, Andrew |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838936/ https://www.ncbi.nlm.nih.gov/pubmed/31720237 http://dx.doi.org/10.1016/j.mex.2019.10.014 |
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