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It can again be seen that cell survival is not significantly different between IGF-I treated and untreated cells in SCM and SFM conditions.

It can be seen that cell death is not influenced by exogenous IGF-I at a 100 ng/ml concentration for all three cell lines in SCM and SFM conditions, even though this concentration of IGF-I significantly increase caspase 3/7, 8 and 9 activities in these cell lines (figure 1 and 2).

Specifically, it can be seen that cells penetrated the inner pores of the scaffold and present like a flattened sheet.

It could be seen that cells treated with the AuNS@PEG nanoparticles at concentrations of 25, 50, 100, 200, 500, and 1000 ppm, respectively (Fig. 3bi vii).

It can be seen that cells self-assembled during 6 to 24 hours and formed network structure at 24 hours, as shown in Fig. 1 (left column).

It can clearly be seen that cells were positive for GFP expression in all cases and that a fraction of the population did not exhibit GFP expression.

It was seen that cell growth was vulnerable only at concentrations wherein the inhibitor is expected to be soluble and when the mode of inhibition was uncompetitive.

In particular, it is seen that cells colonized preferentially the well regions.

It can be seen that the cell types most highly connected within the immune system (such as macrophages and B cells) are also the cell types most connected with body cells.

When considered as a proportion, it can be seen that CD4+CD25+ cells outgrow CD4+CD25– cells from day 7 onwards and remain in significant excess over uninfected controls throughout infection (Fig. 4C).

In Figure 6a, b, it could be seen that the cell with Super P carbon black has better electrochemical and cycle properties than that with AB.