TABLE 2

ChIP-PCR primer sequences and amplification settings

Gene/Clone Primer Name Primer Direction Primer Sequence Fragment Length Annealing Temp.
bp °C
HNF1α Ni16 Forward CATGATGCCCCTACAAGGTT 274 60
Reverse ATTGGAGCTGGGGAAATTCT
ApoB Ni56 Forward GAGGCTCTTCAAGGCTCAAA 181 60
Reverse AACCGAGAAGGGCACTCAG
AAT Ni75 Forward GGAACAGCCACTAAGGATTCTGCAGTGAG 380 60
Reverse TCACTGTCCCAGGTCAGTGGTGGTGCCTG
ANG Ni117 Forward GGGAGATGTACCCCCAAGAG 200 60
Reverse GCTTGTGTGTTTTCCCCAGT
Clone 23, prosite a Ni8 Forward CCAACTCAGGACCTTGGAGA 141 60
Reverse GGCCAGCTTTGCTTCATTAG
Clone 23, prosite b Ni13 Forward GAGCTGCTGTGCCTGGTACT 148 60
Reverse TTTTTGCTGACGGGAGAGAT
Clone 113, site a Ni61 Forward TCATCACGGACATAAAGATGGA 160 60
Reverse GCATAGTGGTGGGGGTTCT
Clone 113, site b Ni73 Forward AGCAGAACCCCCACCACTAT 187 60
Reverse TCACCCAGAAAGTTCCCTTG
Clone 113, prosite a Ni5 Forward CCGGTCAAGTCTGAACCAGT 126 60
Reverse TTAACTAGGCAAGCCCAAGC
Clone 113, prosite c Ni116 Forward TAGTCCCTGTGGCTGCAGTA 232 60
Reverse TCTCAATGGCTGATTACAGGTT