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Cells grown on coverslips were cultured in media with lipoprotein‐depleted serum for 24 h, followed by pulsing with Lysotracker Red DND‐99 (−1 h) and LDL‐pHrodo (0 h). Coverslips were fixed at 1 h (upper panels), 1.5 h (middle panels), and 2.5 h (lower panels) and imaged using confocal microscopy. Scale bar—10 μm.
