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. Author manuscript; available in PMC: 2022 Mar 1.
Published in final edited form as: J Comp Neurol. 2020 Aug 3;529(4):757–785. doi: 10.1002/cne.24977

Figure 1.

Figure 1.

Examples of images obtained from light sheet and confocal microscopes (z-stack maximum intensity projection), both imaged at 5x magnification. Each image was obtained from a perfusion-fixed cochleae immunolabeled with antibodies to myosin VIIa to label hair cells. The dissection process for confocal imaging loses the 3-D architecture that is maintained with LSFM.