Pollen of Lavatera arborea, TESCANProcapsid and nucleocapsid of dsRNA bacteriophage phi6, D. Nemecek, CryoEM Research Group CEITEC, Czech Republic Chroococcus giganteus - Jan Stastny, Charles University, Věda je krásná
Collagen fibers in cartilage, E. I. Romijn, NTNU, Trondheim Pollen grain of Hyoseris radiata, TESCANPlasma coating crossection, TESCAN
Paulinella chromatophora - Yvonne Nemcova, Charles University, Věda je krásnáEudorina - Pavel Skaloud, Charles University, Věda je krásnáButterfly Wings, Benedykt R. Jany, Marian SmoluchowskiInstitute of Physics - Jagiellonian University, Poland
Leaf Fract, TESCANOrchid root with Mycorrhiza, S. R. Senthilkumar, St. Joseph´s College, India Scabiosa columbaria - Viktor Sykora, Charles University, Věda je krásná
1- Gel beads coated with a RuC13 coatings, Magdalena Parlinska, University of Rzeszow, Poland Offretite Scagno, TESCANUniform core shell Fe nanoparticles, S. Bandyopadhyay, NTNU, Trondheim
SEM image of ink-bottle silica nanopores, A. Sterczynska,NanoBioMediacl Centre (CNBM), Poznan, Poland Gold on Germanium, Benedykt R. Jany, Marian SmoluchowskiInstitute of Physics - Jagiellonian University, Poland Polymer fibers, TESCAN
Orchid root showing with idioblastic cells, S. R. Senthilkumar, St. Joseph´s College, India Energy filtered TEM micrograph of yttria (in green) - zirconia (in red) multilayers, Chanchal Ghosh,  IGCAR, Kalpakkam, India  Rhaphoneis - Pavel Skaloud, Charles University, Věda je krásná

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Tuesday, 9 September
Time: 12:30 - 14:00

MAD CITY LABS (20 min)
Room: Small Theatre (1st floor)

Single Molecule Imaging Solutions from Mad City Labs

Single Molecule approaches to understanding biological processes present unique challenges for microscopy. Traditional microscope platforms were not designed to meet these challenges, and often must be modified substantially to do so. We have developed a versatile, modular, open and extensible platform designed around Single Molecule Imaging methods to make customization and innovation straightforward. This system, which we call the RM21™, serves as a framework on which to develop specific imaging solutions. Based on this platform, MCL also offers a multi-wavelength, micro-mirror TIRF (MM-TIRF) microscope designed specifically for studying the composition and ordered kinetics of complex cellular machines. It eliminates multi-band-pass dichroic mirrors, and utilizes a spatially, rather than spectrally separated TIRF strategy to deliver superior signal to noise ratios for single molecule analyses. We have also developed an active stabilization system called the Nano-Cyte® that enables the straightforward implementation of single molecule localization microscopy and volumetric imaging. The Nano-Cyte® can be retrofit onto existing inverted microscope platforms or integrated with the RM21™. These systems can be used together and separately as the core elements of specific Single Molecule Imaging Systems and Solutions.

 

 





 

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