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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...

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書目詳細資料
發表在:MethodsX
Main Authors: Caldon, C. Elizabeth, Burgess, Andrew
格式: Artigo
語言:Inglês
出版: Elsevier 2019
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6838936/
https://ncbi.nlm.nih.gov/pubmed/31720237
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mex.2019.10.014
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