Table 1

Synthetic oligonucleotides and experimental conditions used in reverse transcription-polymerase chain reaction (RT-PCR) analysis

GenePositionFragment size (bp)SequenceCycling numberHybridisation (°C)
β-actin326–3513805′-ATATCGCTGCGCTCGTCGTCGACAA2850
733–7063′-TACATGCATCGGTAGGTCCGACACAA
Ribosomal340–3604865′-GTTCACCAAGGAGGACCTCA23–2550
 phosphoprotein847–8283′-AGACACCTCTGCCTAATGTG
TGF-β1731–7526615′-GAAGTCACCCGCGTGCTAATGG30–3250
1415–13923′-GGATGTAAACCTCGGACCTGTGTG
TGF-β21–221925′-TTCGCAGGTATCGATGGCACCT30–4050
214–1923′-CGTCGTATTAACGACGGAAGCGG
TNF-α3033–30551225′-TTCTGTGAAAACGGAGCTAAAC35–4050
3178–31553′-TTTATTACGACTAAACCACTGGT
TGF-α3538–35573735′-ATGTTGTTCCCTGCAAGTCC25–3050
3930–39113′-ACTATGGAGAGGGGTCGCTT
IL-1β823–8431695′-GCAATGGTCGGGACATAGTT3350
1011–9923′-GAATGTGCCACGGTTTTCTT
SI321–3444325′-TGGGATGATGGCCAATCTAAAGAT3260
776–7533′-ATAGGGATTGTGTTCTGGAGGAAA