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. 2006 Oct 21;12(39):6343–6348. doi: 10.3748/wjg.v12.i39.6343

Table 2.

Primers and restriction enzymes used for genotyping analyses

Gene Primer (5’→ 3’; F = forward; R = reverse) Restriction enzyme
UGT1A7 codon 129 and 131 F1 AAT TGC AGG AGT TTG aTT AA1 VspI
F2 AAT TGC AGG AGT TTG aTT A1 VspI
R1 TTC AGA GGC TAT TTC TAA GA
UGT1A7 codon 208 F3 ATG CTC GCT GGA CGG CAC CAT TG RsaI
R2 TGC CGT GAC AGG GGT TTG GAG A
UGT1A7 allele specific F4 ATT GCA GGA GTT TGT TTA AGG ACA RsaI
R1 TTC AGA GGC TAT TTC TAA GA
UGT1A9 F CAGGTTTTGTGCTGGTATTTCTCCCA
R GCGGATATCCATAGGCACTGGCTTTCCCTGATGACA
ARP G GGCCGGGACTTGGAGGCGGTG
I CAGCACGCTCAGAGCCAG
1

Bold ‘a’ in the primer sequence denotes site-directed mutagenesis for introduction of a VspI restriction site in the wild-type allele.