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For each patient sample, each cell assayed will have some non-negative integer number of copies of each probe.
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RNA was extracted from three Ap-infected and three uninfected samples of each cell line (18 samples total).
Potential participants were allocated to a sampling matrix and a quota randomly sampled from each cell.
RT-PCR was carried out on individual cDNA samples from each cell line.
Five independent biological samples of each cell type were used for qRT-PCR analyses.
Triplicate control and rapamycin samples for each cell line were used in these comparisons.
Then, mean flow velocities were calculated for each layer, calculated from five samples at each cell density.
Using a cell counting chamber placed under a phase contrast optical microscope, 64 samples from each cell type were counted.
The average numbers of TUNEL positive were counted in three randomly selected fields in two tumor samples from each cell line.
Three independent cDNA samples from each cell line were used for each analysis.
Table shows the mean fold change across two samples for each cell line following ATRA treatment.
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