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. 2014 Feb 7;14:28. doi: 10.1186/1471-2180-14-28

Table 2.

qPCR settings and relative transcript abundance

Target gene Primer sequence (5′-3′) a Product size (bp) PCR efficiency Expression ratio b
spxB
fwd: TACCGGAAACTGCTTGGTATC
155
1.93
8.97
rev: CTGGAAAACCGCATCTTTGT
ulaE
fwd: CACTAGCCAAATCAATCGCC
90
2.05
5.78
rev: GCCATCGTCGGTTTCCATTA
xfp
fwd: CGTGAAGAAGGCGATATC
215
2.01
5.98
rev: TTCCAAGTCCACTCCTGA
16S rDNA
fwd: GCYTAACACATGCAAGTCGA
500
1.85
/
  rev: GTATTACCGCGGCTGCTGG      

aPrimer sets were designed based on the sequences of cDNA-AFLP fragments. Primers for 16S rDNA gene were designed as reported by Giraffa et al. [24].

bTarget gene expression was calculated relative to 16S rDNA as a reference gene using the efficiency-corrected ΔΔCT method [23]. The relative expression ratios in CB compared to MRS are shown.