eclipse te 2000-s inverted fluorescent microscope  (Nikon)

Journal: Scientific Reports

Article Title: Graphene Quantum Dots for Cell Proliferation, Nucleus Imaging, and Photoluminescent Sensing Applications

doi: 10.1038/s41598-017-16025-w

Figure Lengend Snippet: CLSM images are showing cellular intake and localization of sGQDs in the nuclei of L929 cells. ( a ) Differential Interference Contrast (DIC) image, ( b ) DAPI localization in the nuclei, ( c ) Red laser excitation is showing localization of the sGQDs from the cell cytoplasm to the nucleus, ( d ) Merged image of all channels, ( e ) Comparative fluorescence intensity plot of DAPI and sGQDs from the selected cells.

Article Snippet: Fluorescence microscopy was performed using Inverted Fluorescent Microscope: Nikon Eclipse TE 2000-S. Confocal laser scanning microscopy (CLSM) was performed using (Olympus, Flow view).

Techniques: Fluorescence

Journal: Scientific Reports

Article Title: Graphene Quantum Dots for Cell Proliferation, Nucleus Imaging, and Photoluminescent Sensing Applications

doi: 10.1038/s41598-017-16025-w

Figure Lengend Snippet: A CLSM imaging showing ( a – d ) qualitative cellular uptake of sGQDs only, and ( e – h ) sGQDs incubated at 4 °C or ( i – l ) at 37 °C with NaN 3 . Other L929 cells were treated with ( m – p ) hypertonic sucrose (0.5 M), ( q – t ) nystatin, and ( u – x ) cytochalasin D up to 8 h.

Article Snippet: Fluorescence microscopy was performed using Inverted Fluorescent Microscope: Nikon Eclipse TE 2000-S. Confocal laser scanning microscopy (CLSM) was performed using (Olympus, Flow view).

Techniques: Imaging, Incubation