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. 2010 Oct;5(10):1805–1814. doi: 10.2215/CJN.01500210

Table 1.

Primer sequences and PCR conditions for amplification of MMP and TIMP SNPs

SNP rs Number Method Primer Sequence (5′ to 3′)
TIMP-1 372 C/T rs 4898 RFLP-PCR Forward GCACATCACTACCTGCAGTC
Reverse GAAACAAGCCCACGATTTAG
TIMP-2 −418 G/C rs 8179090 RFLP-PCR Forward CGTCTCTTGTTGGCTGGTCA
Reverse CCTTCAGCTCGACTCTGGAG
TIMP-2 303 C/T rs 2277698 RFLP-PCR Forward TAGGAACAGCCCCACTTCTG
Reverse CCTCCTCGGCAGTGTGTG
MMP-1 −1607 1G/2G rs 11292517 Fragment analysis Forward 6-fam-CCTCTGATGCCTCTGAGAAGA
Reverse TCCTCCCCTTATGGATTCCT
MMP-2 −735 G/C rs 2285053 TaqMan Allelic discrimination Forward GGGTAAACCTCCCCACATTG
Reverse ACAGTGGAAGGTCCCAGGTT
MMP-2 −1306 C/T rs 243865 ARMS-PCR Forward TGTTGGGAACGCCTGACTTCAG
Reverse CTGACCCCCAGTCCTATCTGCC
MMP-3 −1612 5A/6A rs 35068180 Fragment analysis Forward (6-Fam)CCTGCCTCAACCTCTCAAAG
Reverse AATTCACATCACTGCCACCA
MMP-9 −1562 C/T rs 34016235 Direct sequencing Forward CATAGCTGGAAAATGGCAGA
Reverse TCGGGCAGGGTCTATATTCA

ARMS, amplification refractory mutation system; RFLP, restriction fragment length polymorphism.