In contrast, no pARF5 YFP activity was detected in the same cortical cells (Fig. 2j l).
No other impurities have been detected in the same sensitivity range.
To determine cell boundaries, differences in the intensity levels of CellMask Blue stain were detected in the same channel as Hoechst.
Since no degradation products were detected in the same retention time of β-caryophyllene, the specificity of the method was demonstrated.
In a parallel flow channel, Fe III) was reduced to Fe(II) with ascorbic acid and then detected in the same way as Fe(II).
The main aim was to develop an analytical method, by which both non-polar and polar organic components can be detected in the same run.
Owing to the higher sensitivity, an additional mutation (T790M; including an ultra-low-level mutation, < 0.1%) was detected in the same reaction.
During the in situ study the catalyst appears to reduce further at the induction period of FTS, while crystallite growth is been detected in the same period.
Apart from the soil, no potential for atrazine or mecoprop degradation could be detected in the same samples over a 200-day incubation.
An unclear IS/OS line was also detected in the same area by OCT.
In addition, the QTL for grain weight was detected in the same region, on chromosome 6.
