Bovine Mx1 expression was assessed by Northern blotting and immunofluorescence in the Madin Darby bovine kidney cells (MDBK) cell line treated with several stimuli.
Biological studies were performed to investigate phosphorylation changes in a mouse vascular smooth muscle cell line treated with four different conditions.
Fig. 6 Cell viability of 3T3 cell line treated with SWSB-T20, SWSB-T80, SWSB-PEG, and SWSB-CS for 72 h.
Total genomic DNA from a U251 human glioma cell line treated with ethidium bromide was amplified using primers designed to anneal either mtDNA or a previously described nuclear DNA-embedded mtDNA pseudogene (mtDNAψ).
We used a high power 785 nm laser to measure the time dependent changes in the Raman spectrum of individual living human lung cells (A549 cell line) treated with a toxic agent (Triton X-100, 250 μM solution).
The human fibroblast cell line treated with AgNPs at concentrations of 0.1, 1, or 10 μg/mL for 24 h was analysed using indirect immunofluorescence to detect laminin and collagen-1 production.
The optical microscopic images of the Y79 cells, RB cell line, treated with the peptide, GNPs, and GNPs-Pep-A (Fig. 5) show the morphological differences compared to the untreated cells.
The figure shows in panel A the results obtained for paper samples untreated (red line), treated with PEO hydrogel (black line), or with PLU hydrogel (blue line); and in panel B untreated (red line) and washed with water (green line).
Fig. 1A shows that the SIVs of Tg(fli1 EGFP) zebrafish line treated with 0.1% DMSO at 96 hpf developed as a smooth basket-like structure.
In the large cell line treated with Ca2+ or with Ca2+ plus NPS R-467, CaSR immunostaining increased at cortical level and was reduced in the cytosol.
The BCBL-1 cell line treated with IL-6 was used as a control to monitor the activation of STAT3 and ERK 1/2 [43], [43].
