Difference between revisions of "3-D tracking of single molecules inside cells"
Jump to navigation
Jump to search
| Line 4: | Line 4: | ||
=Description= | =Description= | ||
According to the authors of the study, imaging such highly dynamic processes in the cell and in 3D poses major technical challenges in a complex cell monolayer due to cell-to-cell variations in thickness and temporal properties of protein transport. Previous imaging techniques were slow and suffered from poor z-localization/3D-tracking capability. | According to the authors of the study, imaging such highly dynamic processes in the cell and in 3D poses major technical challenges in a complex cell monolayer due to cell-to-cell variations in thickness and temporal properties of protein transport. Previous imaging techniques were slow and suffered from poor z-localization/3D-tracking capability. | ||
| − | [[Category: | + | [[Category:nanotechnology]] |
[[Category:Nanotechnology]] | [[Category:Nanotechnology]] | ||
Latest revision as of 20:20, 27 August 2020
URL
http://www.nanowerk.com/news/newsid=20451.php
Description
According to the authors of the study, imaging such highly dynamic processes in the cell and in 3D poses major technical challenges in a complex cell monolayer due to cell-to-cell variations in thickness and temporal properties of protein transport. Previous imaging techniques were slow and suffered from poor z-localization/3D-tracking capability.
