Growth of both cell lines was suppressed by 5 and 6 in a fashion dependent on the length of the aminophenol alkyl chain, but not by 3 and 4.
Fig. 6 Migration of both cell lines was affected by GNP-NKCT1.
In addition to pro-inflammatory cytokine secretion by RAW264.7 cells, ROS generation by both cell lines was employed in the present study to compare MWCNT toxicity.
In addition, the topography of both cell lines was investigated by AFM in order to identify and analyze qualitative changes associated with cancer (see Additional file 1).
Viability of both cell lines was high according to the MTT assay after incubation with various SA-FSNP concentrations (Fig. 6a), suggesting that SA-FSNP showed minimal cytotoxicity.
AtT20ins cells, in contrast, exhibited no response to glucose at any concentration tested, despite the fact that insulin secretion from both cell lines was stimulated by incubation with dibutyryl cAMP.
Data obtained from the research demonstrated that the H2DCFDA oxidation in both cell lines was significantly enhanced by treatment with TiO2 NPs for 2 h, reaching its maximum at 6 h, and was reduced at 24 h.
On average, nucleotide diversity in both cell lines was similar, which underpins our previous assumption that the basic mutation rate in both cell lines was similar (Table 4).
DNA extracted from both cell lines was sequenced to confirm cDNA sequences.
The strongest reduction of infection in both cell lines was found with anti-CD151.
HPV-16 expressioninn in both cell lines was confirmed by Western blotting.
