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. 2020 Jul 20;13(14):3227. doi: 10.3390/ma13143227

Figure 1.

Figure 1

Uptake of Aβ by BV-2 cells. (A) Confocal microscopy image after 60 min incubation with Aβ-HiLyte Fluor 488. Magnification 100×. From left to right: DIC (differential interference contrast) microscopy, Aβ-HiLyte Fluor 488 fluorescence, merged. (B) Kinetics of Aβ uptake by microglial cells. BV-2 cells were incubated with Aβ-HiLyte Fluor 488 (0.1 μM) for 0, 5, 15, 30, 60 and 120 min. Fluorescence intensity at 528 nm was measured in six randomly selected cells using confocal microscope. Mean ± SD.