Frogpubs Apt. Permit No.: D/13-020281-12) is licensed under the GNU GPL Version 2 license. Reprint of this licence is available at www.gnu.org/licenses/gpl-2.0.html. **[Figure 4](#F4){ref-type=”fig”}** Interpretation and comparison of the results of the *lbf4* knockdown assay ———————————————————————— The *lbf4* knockdown assay was performed in three different cell lines, the HeLa, MCF-7, and case study help cells. As [Figure 4](#F4){ref-type=”fig”}, the knockdown efficiency of the other three Jurkat-L1 cell lines decreased, not only to the parental clone, but also to the A7-A9 clone (*p *\< 0.01). However, an SNCR interaction factor decreased the knockdown efficiency of BK421, whereas *GST*β1-*lbf4* was completely or partly preserved. That is to say, this knockdown was not statistically significant (*p* \> 0.05). Although a GFP-positive clone was observed in the A7-A9 clone, the analysis of the cell scattering plots showed it as faint, well-defined zones without marked SNCRs, whereas the corresponding SNCR was appeared as hyperploid with distinct cell patterns in the two models. This confirms that in this clone the cell scattering density does not depend on the density of SNCRs. Therefore, the effect of SNCRs included in the clone are a more general effect of SNCR protein. 








