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doi: 10.3945/jn.116.238956 210

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415417 The emergence of stimulated emission depletion (STED) fluorescence microscopy has provided opportunities to directly track lipid flux on the scale of microseconds, and sphingomyelins and gangliosides labeled with the STED-favorable fluorophore Atto647N were used to probe the behavior of sphingolipids in live cell membranes

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