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. 2011 Aug 15;6(8):e23253. doi: 10.1371/journal.pone.0023253

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Khalifé et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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Gel electrophoresis showing the amplification signals obtained by RT-PCR for 8 genes identified by RNAseq as being differentially expressed. The RT-PCR analyses of these 8 genes were congruent with the results obtained by RNAseq. Beta-actin was used as an internal control. PrP + and −: pools of E7.5 FVB/N and FVB.N Prnp-knockout embryo RNAs, respectively.