Wondering how a fully automated confocal microscopy setup could help biologists with rapid acquisition of quantitative imaging data? Check now our new article published in #FEBS Open Bio: febs.onlinelibrary.wiley.com/doi/10.1002/...

Getting SMART about FRAP enabled us to make many FRAP curves in one imaging session. Now we are doing things like 18 conditions n = 30 in a single overnight session. Study protein dynamics in high throughput. Curious on how? see our publication: febs.onlinelibrary.wiley.com/doi/full/10....

We're having a great Functional Imaging and Super-Resolution Microscopy course this year again. With engaged students learning about FRAP, FRET, STED, FLIM and many more (not necessarily 4 letter) fluorescent microscopy techniques. But also a really nice talk by Ben Giepmans about ColorEM.

Fun to see a lightsheet image, made at the Erasmus OIC by Lieke Stockman be awarded with the second prize, in the bruker lightsheet image competition. www.bruker.com/en/products-...

It's the time of the year (just before holiday) where I can do some random stuff to keep the python muscles warm. Here is a simulation of particles with different movement types in different containers. The bubble like structure was hard to code, but it mostly works. youtu.be/2YuseN3GGKc

Sometimes you have to deal with some inevitable truths, like proton beam angle that is fixed. So we flipped a microscope in order to see the effect of proton irradiation on live cells to carefully quantify DNA damage and determine dosage. Read more here: www.sciencedirect.com/science/arti...

I think it would be pretty interesting to see something in the color olo. www.nature.com/articles/d41...

So lets try bluesky as well for science. I'm an assistant professor focusing on advanced fluorescent imaging and image analysis and part of the Erasmus MC Optical Imaging Centre core facility.