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. 2003 Oct;8(4):381–394. doi: 10.1379/1466-1268(2003)008<0381:thsphr>2.0.co;2

Fig 3.

Fig 3.

Immunofluorescence analysis of the intracellular distribution of LpHsp16.1-CIII and its nuclear localization signal (NLS) mutant K75E. Tobacco protoplasts (A) and Chinese Hamster ovary (CHO) cells (B) were used for transient expression of 3HA-tagged Hsp16.1-CIII in its wild type (WT) or NLS mutant form (K75E). As indicated on the left margin, detections were done with HA antiserum (α-HA) and with 4′,6-diamidino-2-phenylindole for nuclear staining. The corresponding nuclei of tobacco protoplasts and CHO cells with detectable Hsp16.1-CIII expression are indicated by arrowheads