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. Author manuscript; available in PMC: 2018 Jan 17.
Published in final edited form as: Cell Rep. 2017 Dec 5;21(10):2706ā€“2713. doi: 10.1016/j.celrep.2017.11.031

Figure 1. Overview of sample collection and processing.

Figure 1

See also Table S1 and Table S2. Primary cultures of astrocytes (Aā€“C) or neurons (Dā€“F) loaded with Mitotracker Red with pre- and post- isolation images of target mitochondrion (red arrows) are shown (B vs. C) and (E vs. F). Scale bars in full size images: 20 microns (A,D), in zoomed images: 5 microns (B,C,E,F). Pixels in the zoomed images were resampled for clarity. (G) Schematic of mtDNA coverage by Round 1 and 2 PCR amplicons. Round 2 PCR reactions were pooled (G, Pooled PCR) prior to acoustic shearing (G, Sheared PCR), and standard Illumina library construction (G, DNA libraries).

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