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. 2021 Feb 16;15(2):e0008913. doi: 10.1371/journal.pntd.0008913

Table 2. Primers and optimized PCR conditions used for transcriptional analysis.

Primer sequence 5’-> 3’ quantity unit [a] annealing (°C) annealing (s) [MgCl2] (mM) [primer] (μM)
RpsL_F1 TCGTACATCGGCGGTGAAG 15U 54 7 5 0,4
RpsL_R1 CCGCGAACCATGTGGTAAC
RpoD_F2 TGCTGCAGGAAGGCAACCTCG 15U 55 5 4 0,4
RpoD_R2 AAATCGCCTGACGAATCCACC
RimM_F2 CGACAACGGCGTGCATTCGATC 15U 50 7 4 0,4
RimM_R2 GCCTTCACGTACACGCCGACGAAC
DnaK_F2 CGAAATCAACCTGCCGTACATC 15U 50 7 5 0,4
DnaK_R2 CGGGTGATCTTCAGATTCAAGTG
RumA_F2 CATCGTCGCGGTCGGCCACA 15U 58 5 4 0,4
RumA_R2 AGCGCAGTTCGGGCTTCACTTC
AmrB_F1 TCGATCAACGTGCTGACGATG 15U 53 9 5 0,6
AmrB_R1 GCAGCTTCTCCTCGACCATCAG
BpeB_F1 CTCGTCGCGTTGATTCTGAC 15U 53 9 5 0,4
BpeB_R1 AGTTGAAGGTGCGGTTGAAC
BpeF_F2 GGCTTCAACAAGGTGTTCCATC 30U 58 5 4 0,5
BpeF_R2 GGAGATACAGGCCGAGCATCACG

[a]: 30 U: 1μL of cDNA in 4 μL water; 15 U: 0.5 μL of cDNA in 4.5 μL water.