Sentence examples for vitro were analysed from inspiring English sources

Immunofluorescent staining of CACs and SMPCs cultured in vitro were analysed with the TissueFAXS system (Tissuegnostics, Vienna, Austria).

In addition, the effects of TbARL6 on tubulin polymerisation in vitro were analysed by measuring turbidity as described previously [34].

To perform this, melanocytes which had been cultured for two passages in vitro were analysed by immunocytochemistry as described in Materials and Methods.

Single-step and multi-step growth in vitro was analysed by infection of BHK-21 cells in suspension for 90 minutes at a multiplicity of infection 5 (single-step growth) and 0.05 (multi-step growth).

Formation of complexes between sRNAs and Hfq in vitro was analysed by gel shift assays.

The biological role of TRIB3 in vitro was analysed in CRC, in which TRIB3 expression was knocked down.

The basal proliferation rate of SVZ-derived cells in vitro was analysed after mechanical cell dissociation and seeding on PO-coated coverslips.

The pharmacokinetic behaviour of the drug in vivo and drug stability in vitro was analysed by gas chromatography with electron capture detection.

Luciferase-expressing MB49 and MB49-I were obtained by stable transfection with the pGL4.50 luc2/CMV/Hygro plasmid (Promega), and selection of hygromycin-resistant subclones displaying similar luciferase activity in vitro was analysed by a Berthold Centro LB 960 luminometer.

Combination treatment of HGS-ETR1 with chemotherapeutic agents in vitro was analysed in HGS-ETR1-sensitive (HCT116 colon, H460 NSCLC) and -insensitive (ES2 ovarian, and TTn oesophageal) tumour cell lines.

Those tumours, which were not further investigated with in vitro MRS, were analysed for bacterial colonization.