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the dynamic action of individual ribosomes - specifically their interactions within polysomes. The key methodologies are optical tweezers, single-molecule fluorescence, as well as selective ribosome profiling
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are depleted via shRNA or CRISPR targeting. You will then capture WPB trafficking events using fluorescence-guided high resolution EM imaging. WPBs and endolysosomal organelles will be labeled using fluorescent
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complementary experimental approaches to understand the underlying bubble physics. These include ultra-high-speed imaging of bubble dynamics at up to ten million frames per second and laser-induced fluorescence
Searches related to fluorescence imaging
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