Cells were seeded in cell culture-treated 384 multi-well plates in the respective medium (A). After overnight incubation at 37 °C, compounds are dispensed by a Nanodrop Tecan D300e machine (B). Cells are treated for 72 h at 37°C at 5 % or 10% CO2 (C). Finally, cell plates are equilibrated to room temperature and the viability of cells is determined with CellTiter-Glo luminescent reagent based on the amount of ATP present (D).
The semi-automated screening process produces highly reproducible data. In every run bortezomib serves as the control reference compound. Shown here are the mean data and standard error of bortezomib results from 4 independent ProLiFiler runs.
Identification of cell lines sensitive to the MET kinase inhibitor Crizotinib. Crizotinib was tested for anti-proliferative and cytotoxic capacity with the ProLiFiler cell line panel. Three cell lines were most receptive to treatment including MKN-45, LOVO, and Karpas 299.
Identification of the tumor origin most sensitive to the MET kinase inhibitor Crizotinib. IC50 values of Crizotinib potency on a panel of tumor cell lines were sorted based on the tumor entity. Colon tumors (red) were most susceptible to treatment.
Our bioinformatics analysis tools are available to identify the mechanism of action of your test compound and to detect suitable biomarkers for stratification of responders vs. non-responders.
To offer these analytic tools, we have partnered with 4HF Biotec GmbH, a bioinformatics firm specializing in cancer data mining to discover new anti-cancer drugs. 4HF Biotec performs the data mining analysis based on their proprietary database and provides hands-on support with a high focus on client communication to answer your key questions.
Setup: IC50 determination or single concentration testing with CellTiter-Glo readout. Drug combination testing is also an option, see an example study here.
Controls: DMSO only treatment serves as high control. Staurosporine treatment (at 1x10-5M) serves as the low control. In every project, the IC50 value determination of a reference compound is included.
Report: A detailed report including assay conditions, methodology, and comprehensive evaluation of data as well as raw data for each analysis will be provided.
Screening schedule: Please find the screening schedule here. Results are available after 6 weeks.
Testing of subsets: For testing a subset of cell lines, or single concentration screening of multiple compounds, please see our Cell Proliferation Assay service with the free choice setup here.
Screening Facility: The ProLiFiler cell line panel screening is performed in Freiburg, Germany.
Compound requirements: In brief: 100 µl of the stock solution with 1000x the highest testing concentration or the equivalent as solid material.