Sentence examples for microscope cells were from inspiring English sources

Using a multitrack and line-scanning mode of a laser-scanning confocal microscope, cells were simultaneously recorded in the CFP and YFP, and FRET detection channels.

Using multitrack and line-scanning mode of a laser-scanning confocal microscope, cells were simultaneously recorded in the CFP and YFP detection channel.

Prior to mounting on the microscope, cells were washed twice with PBS [ 12].

Directly after image acquisition at the microscope, cells were washed twice with sterile PBS and then lysed on ice for 10 min in lysis buffer as previously described or RIPA buffer (50 mM Tris, 150 mM NaCl, 1% Triton X-100, 2 mM EDTA, 0.5% DOC, 0.1% SDS, complete protease inhibitor cocktail mix, Roche).

To enable imaging in the third channel of the microscope, cells were grown in twelve-well plates on 13 mm diameter coverslips to a density of 8 × 10 and left to grow overnight under the conditions described above, then Laurdan-stained prior to bead incubation as described above.

Ectopic expression of each construct was detected by a fluorescence microscope (Olympus IX53 inverted microscope), and cells were stained for TRAP.

To examine the cellular uptake of nanoparticles via fluorescence microscope and confocal laser microscope, the cells were seeded at a concentration of 1 × 10/mL in a 10 mL Petri dish and incubated for 1 day.

In order to visualize vessels under a fluorescence microscope, the cells were incubated with calcein-AM (2 µM) for 20 min. Pictures were taken with an Olympus fluorescence microscope (Olympus).

Under a fluorescence microscope, the cells were observed with brown precipitate were the result of positive apoptosis.

Remarkable morphological changes were observed under the fluorescence microscope when cells were treated with cisplatin-functionalized particles.

Under a biological microscope, the cells were observed that where brown precipitate was the result of positive apoptosis [25 27].