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. 2020 Jan 20;9:8. doi: 10.1038/s41377-020-0245-8

Fig. 4. Volumetric CLAM imaging of light-scattering fluorescence microbeads embedded in agarose gel.

Fig. 4

The imaging depths are (a, e) 30 μm, (b, f) 100 μm, (c, g) 200 μm, and (d, h) 300 μm; the top right half of the images in (c, d) are denoised for a comparison. The depth is color-coded in (ad). eh show the maximum intensity projections (left) and linear intensity profiles (right) of the beads marked in (ad). i SNR as a function of the penetration depth. Image denoising is applied for a comparison at the deeper depth. The scale bars represent 40 μm (ad) and 5 μm (eh).