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FE-SEM analysis of cell-scaffold construct illustrated the cell adhesion of L929 mouse fibroblasts on the surface of scaffold.
For this reason, a variety of elements were removed from the inverted repeat-intron construct (illustrated in Fig. 1) and their ability to induce gene silencing assessed.
Histology of the construct illustrated that cells were aligned to the fiber directions in the construct, demonstrating the potential to control the microstructure of tissue-engineered vascular grafts using the electrospun scaffold membrane.
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Five such target paths were constructed, illustrated in Fig. 1.
A Venn diagram was constructed illustrating the degree of overlap among genes modulated by 5-AZA-CdR, in the tissues under investigation.
HEK-293 cells were transfected with expression plasmids encoding the various HIC constructs (illustrated in Figure 3A).
Equal amounts of in vitro transcribed RNA from the various constructs illustrated in figure 3A were translated using a rabbit reticulocyte lysate system (Fig. 3B).
The resulting seven promoter deletion constructs (illustrated in Figure 1) were all fused to the BB cDNA and transformed into bb-1 mutant plants.
The exception handling construct is illustrated by a real application excerpt.
The resulting plasmid construct is illustrated in figure 1A.
The resulted pPF-Lib-p3 library construct is illustrated in Figure 1B and C. All steps of the phage display selection and analysis of individual peptide-displaying clones were carried out as previously described [70].
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