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Correlative fluorescence microscopy, transmission electron microscopy and secondary ion mass spectrometry (CLEM-SIMS) for cellular imaging

Fig 2

A large-view CLEM image.

A large field was imaged in both TEM and fluorescence, relying on the DAPI (blue) channel, which shows the uranyl acetate fluorescence, and on the mito-mCitrine channel (shown here in green). Scale bar: 10 μm. Boxed region 1 shows a higher zoom view on the light microscopy image as well as the correlated image with TEM of a cell marked by a white square in the overview image. Scale Bar: 2 μm. Boxed regions 2 and 3 show detailed images of CLEM and TEM in the regions of interest. Scale bar: 1 μm.

Fig 2

doi: https://doi.org/10.1371/journal.pone.0240768.g002