Expanding the limits of EM sample prep with ICE
Listen now
Description
In this webinar you will learn: - Improved vitrification: Specimen vitrification without synchronisation fluid - Vitrification strategies: Optimized freezing for different techniques - Light and electrical stimulation: Dissect cellular processes with millisecond precision - A look into the future: freezing of crystals Plunge freezing and cryo imaging of proteins and complexes have revealed new details in understanding the machinery of the cell and how molecules are involved in cellular processes. However, most eukaryotic cells and tissue samples cannot be plunge frozen because of the rapid decay of the cooling rate within the sample during freezing. High pressure freezing, on the other hand, is currently the main approach to vitrify larger samples (up to 200 µm) and to capture the intrinsic changes in fine structure or cellular dynamics. To further improve its cryo solutions, Leica developed a new cryo platform: the EM ICE. This new generation cryo platform combines speed, reliability and flexibility to facilitate research in various scientific fields. The EM ICE allows users to freeze samples within milliseconds and even permits the combination of high pressure freezing with optogenetics and electrophysiology.
More Episodes
#29 — Ever wondered why you have to add protease inhibitors to your lysis buffer? In this episode of Mentors At Your Benchside, we’ll tell you all about protease inhibitors, why they’re important and how to use and store them. To learn more about protease inhibitors and to access the table with...
Published 09/27/22
Published 09/27/22
#28 — SDS-PAGE gels can be run at constant current, constant voltage, or constant power. But which is best? Listen to this episode of Mentors at Your Benchside to discover the differences between current, voltage, and power, and how they affect how your gels run. Visit the original article for a...
Published 09/22/22