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. Author manuscript; available in PMC: 2009 Mar 9.
Published in final edited form as: Drug Metab Dispos. 2005 Apr 8;33(7):937–946. doi: 10.1124/dmd.104.003061

TABLE 1.

Primers and conditions for semi-quantitative PCR analysis. Nucleotide sequences are reported for primer pairs used in RT-PCR analysis experiments in HepG2 and Caco-2 cells.

Target Transcript Primer Set Annealing Temperature Amplicon Size No. of Cycles on HepG2 cDNA No. of Cycles on Caco-2 cDNA
°C bp
FXR F: ggaaccatactcgcaatacagc 56 402 31 32
R: tcgcatgtacatatccatcacac
PXR F: caagccaagtgttcacagtgag 60 818 35 35
R: caaagagcacagatcttccg
UGT2B7 F: agttggagaatttcatcatgcaacaga 58 232 26 30
R: tcagcccagcagctcaccacaggg
I-BABP F: gacttaggggctgagcctcagca 60 491 34
R: ttgctcacgcgctcataggtcac
GAPDH F: acccactcctccacctttg 64 178 25 25
R: ctcttgtgctcttgctggg

F, forward primer 5′-3′; R, reverse primer 5′-3′.