Livecyte: Creating a comprehensive cell profile


Published: 17 October 2019
Abstract Views: 694
PDF: 348
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Authors

Live-cell time-lapse microscopy is an established and powerful technique for the study of mammalian cell biology in vitro. Common time-lapse applications use label-free and/or fluorescence approaches, with the latter requiring introduction of dyes or labels. For many label-free techniques, constraints caused by low levels of contrast preclude the automated segmentation of individual cells, and by association, the capability to differentiate them based on subtle differences in their phenotypic or kinetic characteristics. On the other hand, fluorescence microscopy overcomes such contrast limits, but labels have the potential to alter normal cell function and induce toxicity. Phasefocus Livecyte uses ptychography to generate high-contrast, label-free yet fluorescent-like images, using low powered illumination, allowing for robust individual cell segmentation during long-term time-lapse experiments.


Ethics Approval

<blockquote class=

Anselmi, G., & Humphry, M. (2019). Livecyte: Creating a comprehensive cell profile. Microscopie, 30(2). https://doi.org/10.4081/microscopie.2019.8592

Downloads

Download data is not yet available.

Citations