Below we show representative images and videos as examples of the range of techniques, scales and samples investigated within the CoB.
Calcium flux in a living mouse brain section expressing a genetically encoded calcium indicator. Stimulation was performed using a pulse of hyperkalemic solution. [Tello lab]
Contractility mapping of the zebrafish heart using light-sheet microscopy with acoustic sample confinement. Scale bar is 50 μm. Yang et al. Nature Communications 10, 669 2020. [Somorjai lab] [Dholakia lab]
Two larval epithelial cells undergo pulsed contractions during Drosophila abdominal morphogenesis. The cells’ actin cytoskeleton is labelled with a GFP-reporter. Pulido-Companys et al. J. Cell Sci., 133 (6) 2020. [Bischoff lab]
Large field of view fluorescence video-rate microscopy of neonatal cardiomyocytes . Cells were labelled with SiR-actin to visualize sarcomeric actin. [Schubert lab] [Pitt lab] [Miles lab] [Gather lab]
DIC microscopy time-lapse video of a spontaneously beating neonatal cardiomyocyte showing an internalized microlaser as circular object in the centre of the cell. Schubert et al, Nat. Photonics, 15, 452, 2020. [Schubert lab] [Pitt lab] [Miles lab] [Gather lab]
Drosophila abdominal morphogenesis. Histoblasts replace larval epithelial cells during formation of the adult epidermis. Nuclei of both cell types are labelled with Histone-GFP. Bischoff and Cseresnyes, Development 136, 2403 (2009). [Bischoff lab]
Maximum intensity projection of light sheet fluorescent microscope images of optically trapped tobacco BY-2 cells expressing microtubules labeled with GFP. Scale bar 15 µm. Yang et al, Biomed. Opt. Express 6, 2778-2785 (2015). [Ferrier lab] [Gunn-Moore lab] [Dholakia lab].

Fluorescent imaging of muscle activation during locomotion in Drosophila larvae using green fluorescent protein. Red: image sequence showing peristaltic wave of muscle contraction corresponding to forward locomotion, Blue: peristaltic wave during backward locomotion, Green: muscle activation during head sweep behaviour. [Pulver lab]
Light-sheet microscopy of cell and tissue behaviours during primitive streak formation in Myr-GFP embryos. Robzicki et al. Nat. Cell Biol. 17, 397, 2015 [MacDonald lab]