Mouse fibroblast cell line L929 (ECACC; L929 (NCTC); #85103115) was purchased from Sigma-Aldrich (Taufkirchen, Germany).
A L929 mouse fibroblast cell subline was chosen based on its high susceptibility to prion strains 22L and RML24, 28.
Thermally oxidized Mg Al alloy (AZ91) treated at 200 °C for 25 h have shown best biocompatibility in terms of cell (L-929 mouse fibroblast cell line) proliferation.
Besides, the effect of the synthesized compounds on mouse fibroblast cell line (L929) was simultaneously evaluated as control.
In this work, we present studies of mouse fibroblast cell activity grown on gallium nitride surfaces after applying external noxa.
The bacterial strains of Pseudomonas aeruginosa (ATCC 27853), Staphylococcus aureus (ATCC 6538) and 3T3 mouse fibroblast cell line (ATCC 1658 were originally obtained from American Type Culture Collection (ATCC).
Improved cell adhesion to the HAp nanocrystal-coated surface was demonstrated by in vitro testing using a mouse fibroblast cell line L929.
The standard model mouse fibroblast cell line together with the MTT and NR tests were utilized for evaluating the toxicity of the prepared compounds.
Moreover, compounds 12c and 17c did not exhibit obvious cytotoxicity in either cancer cell lines or normal mouse fibroblast cell lines.
The mouse fibroblast cell line L929 was inoculated on 3D scaffolds of microbial polyesters, namely polyhydroxybutyrate (PHB) and poly(hydroxybutyrate-co-hydroxyhexanoate) (PHBHHx) to evaluate their in vitro biocompatibility.
A mouse fibroblast cell line carrying a recoverable lambda phage shuttle vector for mutation detection was transfected with either a vector designed to express hPMS2 or with an empty vector control.
