PMC:4307275 / 13336-14196 JSONTXT

{"target":"http://pubannotation.org/docs/sourcedb/PMC/sourceid/4307275","sourcedb":"PMC","sourceid":"4307275","source_url":"https://www.ncbi.nlm.nih.gov/pmc/4307275","text":"Taken together, these results suggest that the sGFP targeting into chloroplasts using rRTp plays an important role in improving the fluorescence intensity of FCA to increase the population with higher fluorescence than the threshold value, as well as to increase its average fluorescence intensity (\u003e8-fold). However, the results of hemocytometer analysis (right panels of Figure 2C) do not correspond to the data of fluorescence intensity (left panels of Figure 2C) on FCA, in the point that the histogram analyses of those images showed that the mean intensity ratios between K-sGFP and KR-sGFP were similarly determined, as shown by scale bars (Figure 2C). Supposedly, the difference of fluorescence intensity on FCA data between K-sGFP and KR-sGFP might not be derived from the difference on the molecular levels of RNA/proteins or transfection efficiency.","tracks":[]}