Table 1.
Gene (2-DE spot) | Forward primer (5′-3′) Reverse primer (5′-3′) |
aTa (°C) | Amplicon size (bp) |
---|---|---|---|
omp (spot 14) | F: ACTCGTGGCTCTACTACG | 50 | 381 |
R: ATGCGTTGTTATACAGG | |||
| |||
omp (spot 15) | F: ATCACGGCACAAGACGC | 60 | 255 |
R: AGCGTTCTGAGCAGCGAACG | |||
|
|||
for RT-qPCR | F: GCGCTGGCAACCTGCGTTCG | 60 | 166 |
R: GTGCGCTTGGACAGCGCGTA | |||
| |||
rps (spot 16) | F: AAGCGCCAGTCGCGTGAGATCC | 60 | 407 |
R: TTGCTCGAGTCGTCGTTACC | |||
| |||
dps (spot 17) | F: TCAAGACCCACAACTTCC | 54 | 249 |
R: TGACGGACTCGTGACCG | |||
|
|||
for RT-qPCR | F: GGACCGCCGTGGATTCGGTGG | 60 | 189 |
R: CCGGGAACAGGCTGCGTGCG | |||
| |||
epsD (spot 18) | F: TGCTGGAATCCACTTCG | 50 | 360 |
R: TCTCATCACAGATCATCG |
Annealing temperature for PCR amplification