Combining and multiplexing microscopy approaches is crucial to understand cellular events, but requires elaborate workflows. Here, we present a robust, open-source approach for treating, labelling and imaging live or fixed cells in automated sequences. NanoJ-Fluidics is based on low-cost Lego hardware controlled by ImageJ-based software, making high-content, multimodal imaging easy to implement on any microscope with high reproducibility. We demonstrate its capacity on event-driven, super-resolved live-to-fixed and multiplexed STORM/DNA-PAINT experiments.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420627PMC
http://dx.doi.org/10.1038/s41467-019-09231-9DOI Listing

Publication Analysis

Top Keywords

automating multimodal
4
multimodal microscopy
4
microscopy nanoj-fluidics
4
nanoj-fluidics combining
4
combining multiplexing
4
multiplexing microscopy
4
microscopy approaches
4
approaches crucial
4
crucial understand
4
understand cellular
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!