HIGHLIGHTS
- who: Hugh from the NY, USA have published the paper: Rafael Nunez*, in the Journal: (JOURNAL)
SUMMARY
The standard benchtop flow cytometer is very similar to a hematology cell counter. As particles or cells flow in single file past the intersection of the light beam, light is scattered in various directions. If there a fluorochrome labeled monoclonal antibody associated with the cell, it becomes excited by the laser and a fluorescent emission results. The cytometer itself is set up and monitored routinely with a quality_control program utilizing a series of unlabeled and fluorescently . . .

If you want to have access to all the content you need to log in!
Thanks :)
If you don't have an account, you can create one here.