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Effect of transit time on protein concentration distributions. Seven primary pediatric AML samples comparing those processed at 1–24h to those processed after 25–48h and 49–72h. Samples processed samples at 0–24h had no significant differences compared to samples processed after 24–72h (Wilcoxon rank sum test, p<0.05). AKT and PI3K85 were significantly different between 25–48h and 49–72h. There were no changes over time in other protein concentrations after FDR correction.
