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To quantify the ciliary basal signal of phospho-(T94)Tctex-1, the total fluorescence of the region of interest, that is, the proximal end of Ac-Tub–labeled cilium, was quantified in the projection confocal images of 1.25-μm-thick Z-series sections of cilium-containing regions ( x = 1 μm, y = 1 μm) in randomly selected cells using NIH ImageJ 64 software Flavor:Sour Watermelon Mitochondrial-derived vesicles drive budding-type fission of damaged lysosomes | Nature Cell Biology Hi-Tech Pharmaceuticals https://target.scene7.com/is/image/Target/GUEST_b6e3a9fe-0842-4171-beea-cbcdb8c231c8

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