Furthermore, flexibility of the organotypic system allowed us to use PSCs that had been treated with FGFR1 RNAi to demonstrate that this regulation of stellate cell invasion, and modulation of cancer cell behaviour, is specific to FGFR1.
The use of the system allowed us to include a yeast origin of replication into the TAR vector and to select TAR cloning events against vector recircularization.
Indeed, the use of retroviral system allowed us to obtain a considerably higher percentage of scFv-expressing cells, as assessed by counting immunofluorescent scFv-positive cells.
Even after methotrexate amplification, the expression of these antibodies by the CHO cells is low, in comparison with the amounts produced by hybridoma cells, but use of a commercial system allowed us to obtain milligram yields of purified recombinant antibody.
The use of a conditional expression system allowed us to study the fate of newly synthesized Pex3 chimeras during pulse-chase experiments even if these mutants were instable.
The use of an integrated drop visualization system allowed us to examine in situ the drop volumes and velocities and to access the optimum printing parameters window.
Experiments using the above ice particles and the system allowed us to obtain 3D microscopic images.
This system allowed us to demonstrate that recombination activity could be detected when using a dsattC, even if this process was strongly increased when the bsattC was provided.
Collectively, use of soluble peptide analytes and immobilized HSP72 in the BIAcore system allowed us to model solution interactions between HSP72 and viral RNP.
An extensive tram system allowed us to visit outlying attractions including the car and train museums.
Recently the system allowed us to make only basic entries and we couldn't access reports all day.
