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. 2016 Mar 23;7(4):236–249. doi: 10.1007/s13238-016-0254-9

Figure 6.

Figure 6

RT-qPCR verification of the RNA-Seq results. The 8 randomly selected genes (TTHERM_00961910; TTHERM_00730300; TTHERM_00426250; TTHERM_00077290; TTHERM_00865200; TTHERM_00338290; TTHERM_01109940; TTHERM_00763040) plus CYC2 TTHERM_00079530) and SPO11 (TTHERM_00627090) were performed with RT-qPCR. The primers were designed to across an intron to eliminate potential confluence from residue genomic DNA contamination. cDNA templates were from of 3 independent biological repeats of cell samples respectively at 2 h (A), 2.5 h (B), 3 h (C), and 3.5 h (D) after conjugation initiation. The tendencies of mRNA expression changes were in accordance with the RNA-Seq analysis results, which well-validated of the sequencing data