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. 2010 Jan 26;8(1):e1000288. doi: 10.1371/journal.pbio.1000288

Figure 2. Subcellular localization of TAP38.

Figure 2

(A) Full-length TAP38-RFP was transiently expressed in Arabidopsis protoplasts and visualized by fluorescence microscopy. Auto, chlorophyll autofluorescence; DIC, differential interference contrast image; merged, overlay of the two signals; RFP, fusion protein. Scale bar indicates 50 µm. (B) 35S-labeled TAP38 protein, translated in vitro (lane 1, 10% translation product), was incubated with isolated chloroplasts (lane 2), which were subsequently treated with thermolysin to remove adhering precursor proteins (lane 3), prior to SDS-PAGE and autoradiography. m, mature protein; p, precursor. (C) Immunoblot analyses of proteins from WT and tap38-1 leaves. Equal protein amounts were loaded. Filters were immunolabeled with a TAP38-specific antibody. Chl, total chloroplasts; Str, stromal proteins; Thy, thylakoid proteins; Tot, total protein.