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. 2005 Jan-Dec;11(1-12):30–38. doi: 10.2119/2005-00038.Gagliano

Table 1.

Primer sequences and RT-PCR amplification conditions.

Gene Primer sequence Annealing temperature, °C No. of cycles Product size, bp
COL-I 5′-TTGACCCTAACCAAGGATGC
5′-CACCCCTTCTGCGTTGTATT
54 30 197
COL-III 5′-AGGCCAATGGCAATGTAAAG
5′-GGCCTTGCGTGTTTGATATT
53 30 187
TGF-β1 5′-CACCTGCACAGCTCCAGGCAC
5′-CTTGCGACCCACGTAGTAGACG
54 32 153
HGF 5′-TCGTTCCTTGGGATTATTGC
5′-TGGTGCTGACTGCATTTCTC
55 32 571
TIMP-1 5′-TCCCCAGAAATCATCGAGAC
5′-ATGGCTGAACAGGGAAACAC
55 32 329
LH2b 5′-TGCGATCAGAGATGAGTGAA
5′-GTTGAGATGGGAAGTGTTGTAAT
53 32 229
E-cadherin 5′-GCAGTTCTGCCAGAGAAACC
5′- AATCCTGCTTCCAGGGAGAT
55 28 315
N-cadherin 5′-TGTTGCTGCAGAAAACCAAG
5′-GGCGACTCTCTGTCCAGAAC
53 28 309
DSG-2 5′-CCTTGGTGGACCAGCACTAT
5′-GACAGCACCGTCTTCCTAGC
57 35 316
DSC-2 5′-CGTAATTCCCGTCCGAGTTA
5′-TTGAGCTGTGAAGCCATTTG
55 35 386
GAPDH 5′-ATGGTGAAGGTCGGTGTGAAC
5′- GCTGACAATCTTGAGGGAGT
54 28 473