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. 2009 Dec 24;5(12):e1000705. doi: 10.1371/journal.ppat.1000705

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Barajas et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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(A) Confocal laser microscopy images show the subcellular localization of Vps23p-GFP in the presence of p33 expressed from CUP1 promoter for 15–45 minutes in yeast strain DKY79 (VPS23:GFP, vps4Δ; vps27Δ). The peroxisomes were visualized with Pex13p-RFP marker. The merged images show the co-localization of Vps23p-GFP and Pex13p-RFP marker. DIC (differential interference contrast) images are shown on the right. Each row represents a separate yeast cell. (B) Cytosolic localization of Vps23p-GFP in the absence of p33. Yeast was grown under similar conditions and images were taken as in panel A.