goodness! thank you Agreed, thorough and clearly explained❣ I really like your including comparisons of other microscopy techniques helps us understand how combining multiple microscopy capabilities can aid in achieving ideal testing. phenomenal!
hello, why the LSFM is diffraction limited and on wikipedia in french there is write that Sidentopf and Zigmondy manage to pass the diffraction barrier with the ultra microscope
making light sheets is not nessesary because the objectiv and foto stacking have this possibility and fluorescenc-microscopy still gives unsharp images. Light sheets are still thicker than tocal plane sharpness. Here much theory is given but i see no results
Great video! All very clearly explained, thank you!
This is so thoroughly explained. Thank you very much!
goodness! thank you
Agreed, thorough and clearly explained❣
I really like your including comparisons of other microscopy techniques helps us understand how combining multiple microscopy capabilities can aid in achieving ideal testing. phenomenal!
That's a great video on the topic! Thank you for this thorough presentation.
Amazing - thanks a lot for this resource, super clearly explained, useful, and kind of you to upload this for free.
Amazingly clear talk! Thank you so much
hello, why the LSFM is diffraction limited and on wikipedia in french there is write that Sidentopf and Zigmondy manage to pass the diffraction barrier with the ultra microscope
men for real thank you make me feel better on this subject !
Great cover. Appreciate!
Amazing thank you!
Thanks a lot!
Thx, it helps a lot
making light sheets is not nessesary because the objectiv and foto stacking have this possibility and fluorescenc-microscopy still gives unsharp images. Light sheets are still thicker than tocal plane sharpness. Here much theory is given but i see no results