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. 2014 Oct 4;67(3):545–550. doi: 10.1007/s10616-014-9785-1

Fig. 1.

Fig. 1

Activation of MAPK–JNK by HEV replicon-synthesized ORF3 in S10-3 cells. a Agarose-gel electrophorogram, showing in vitro transcribed viral genomic RNA. Lanes 1 pSKE2; 2 negative control; 3 DNA marker. b Immune-fluorescence microscopy (IFM), showing co-expressions of HEV ORF2 [chimp sera (10Ab; 1:100) & Alexa 488-conjugated goat anti-human IgG (20 Ab; 1:100)] and ORF3 [rabbit anti-ORF3 (10Ab; 1:500) & Alexa 568-conjugated goat anti-rabbit (20Ab; 1:100)] proteins in RNA-transfected cells at day4. c Phospho-ELISA, showing ex vivo activation (%) of phospho-JNK1/2 (day4, p.t.) in cells supporting HEV RNA replication and gene expression: wt: pSKE2-wt (red); GAD: pSKE2-GAD (yellow); Mock: untransfeted (green)