After becoming adult worm, pqbp-1.1-Venus expression reduced rapidly in pharynx, while the expression continued in intestinal cells (Fig. 4).
As shown in Figure 2, the peak levels in the tumour tissue were observed 3 days after the injection and the expression continued for more than 10 days.
The miRNA was up-regulated regardless of whether the fruit was stored at 1 °C or 25 °C, while the expression continued to decline when fruit was kept for 24 h and 48 h at 25 °C after cold storage (Fig. 4c).
GFP fluorescence was first detected in P(5−7).p daughters, and the expression continued in their progeny in the L3 and L4 stages, when cells acquire a specific fate (vulA to F) and undergo morphogenetic changes.
At the time when the Amphimedon embryos begin to display anterior-posterior polarity, Wnt expression becomes localised to the posterior pole and this expression continues until the swimming larva stage.
The Wnt expression domain overlaps with the pigment spot and ring (Fig. 2G I) and this expression continues within the pigment ring in the free swimming larva (Fig. 2J).
Examination of connexin expression patterns in the mouse reveals that Cx40 and Cx45 are co-expressed both in Purkinje myocytes and in the underlying transitional cells, and that the Cx45 expression continues down into the most superficial layer of ventricular myocytes.
Oddly, the GFP expression continues to be elevated in mature thymocytes and even in peripheral T cells.
When these promoters are inhibited by the anti-sigma factor, the σ factor expression continues from the phage-specific promoters.
In culture, the differential gene expression continues to reflect their site of origin, and the phenotypes of S-Bdc and L-Bdc differ.
