Additional file 22.

Raw data of the proteomic analysis, using 2DGE, following the induction of two Runx1 overexpressing clones (E6 and E7). Three technical repeats were performed for each biological replicate: this comprises 6 gels for E6 and 6 gels for E7. For each clone we ran three replicates for t0 (control) and three replicates for t48 hours. Corresponding t0 and t48 hour samples were always run simultaneously in the same chamber to ensure gel pattern comparability. The detailed spot quantification data are provided in this table. We list the relative volume of each spot on each individual 2DGE gel, together with other spot parameters, such as pixel spot volume, x and y coordinates of spots on the fusion gel image, as well as spot quality index.

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De Cegli et al. Genome Biology 2010 11:R64   doi:10.1186/gb-2010-11-6-r64