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. 2017 Nov 1;95(6):579–591. doi: 10.1007/s11103-017-0672-y

Fig. 3.

Fig. 3

Localization of HSP22E/F to the chloroplast. a Subcellular localization of HSP22E/F by immunoblotting. 10 or 3 µg protein (depending on the antiserum used) from whole cells (input), chloroplasts (cp) and mitochondria (mt) isolated from strain cw15-302 exposed to 39 °C for 60 min were separated by SDS-PAGE and immunodetected with antisera against HSP22F, mitochondrial carboanhydrase (mtCA), extrinsic thylakoid membrane protein CF1β, and stromal HSP70B. b Microscopy images taken from cells of strain cw15-325 that were kept at 25 °C or exposed to 39 °C for 60 min. Shown are from top to bottom: bright field (BF) images, DAPI staining, immunofluorescence (FITC), and the merge of DAPI and FITC. Antisera used for immunofluorescence were against HSP22F, stromal RbcL, and cytosolic HSP70A