I have some questions about microscopy that I do not fullyunderstand:
Single particle tracking (SPT)
Fluorescence recovery after photobleaching (FRAP)
Stimulated emission depletion (STED)
1. Are those each a microscope or is it atool that are used by microscopes?
2. There are different fluorescence microscopes; wide-field,confocal and Two-photon microscopes.
DO we have only ONE fluorescence microscope which by changingthe light and filter makes it to widefield microscopy? Or are thosenames (wide-field, confocal and Two-photon microscopes) eachdescribing an individual microscopy?
I have some questions about microscopy that I do not fullyunderstand:
Single particle tracking (SPT)
Fluorescence recovery after photobleaching (FRAP)
Stimulated emission depletion (STED)
1. Are those each a microscope or is it atool that are used by microscopes?
2. There are different fluorescence microscopes; wide-field,confocal and Two-photon microscopes.
DO we have only ONE fluorescence microscope which by changingthe light and filter makes it to widefield microscopy? Or are thosenames (wide-field, confocal and Two-photon microscopes) eachdescribing an individual microscopy?
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