TABLE 1

Primer sequences used for the amplification of the BCRP gene fragment and the annealing temperatures used in the PCR


Name

Region

Primer Sequence (5′→3′)

Size

PCR Condition
base pair Tm; °C
BCRP1P Promoter F: AACCCAGCTAGGTCAGACGA 557 60.0
R: TTTGAGTGGGCACAGCAC
BCRP2P Promoter F: TTCCTAGGGTAGATGCAGCAG 509 60.0
R: CAGGGACAAGCCAAACACTC
BCRP3P Promoter F: GTAGAGGCAGGGTTTCACCA 559 60.0
R: AAGTGATTGCGCATGTTCAG
BCRP4P Promoter F: CGTGCCTGGCCTCTATGTAT 572 60.0
R: CTGACGCAGGCAGATCACT
BCRP5P Promoter F: GCCACCACACCCAGTGTAAT 518 64.7
R: TGCAAAGTAAAAACAAATCAAAACC
BCRP1E Exon 1 F: AGCTCGTCCCCTGGATGT 516 54.0
R: CCACCAACCTTTCCAGACAC
BCRP2E Exon 2 F: CTGCTCATTGCCACACATTT 400 54.0
R: GCCAAAACCTGTGAGGTTCA
BCRP3E Exon 3 F: GTCTCAAACTCCTGGCCTCA 403 54.0
R: GCGTTGCAAATGCTCAATAA
BCRP4E Exon 4 F: TGGATTCAAAGTAGCCATGAGA 402 54.0
R: ATTCTCCCTGCCTTTTCACA
BCRP5E Exon 5 F: GGTTCATCATTAGCTAGAACTTTACC 403 54.0
R: TGGAAAGCAACCATTTTTGA
BCRP6E Exon 6 F: TCTTACAGGACTGGCACACG 426 54.0
R: CCTTCCCTACATTCTTACCTGCT
BCRP7E Exon 7 F: TCAGGCTGAACTAGAGCAAACA 387 60.0
R: AGCACCAAATGGAACAAACA
BCRP8E Exon 8 F: CATGGGAAGAAGAGAGAAAGAAA 412 60.0
R: CAAAAACACCAACAGCACTCA
BCRP9E Exon 9 F: GGTGTTAGGGAAGCATCCAA 413 54.0
R: TGAAGCAGATGATAACAGAACCA
BCRP10E Exon 10 F: GCCAAGCCATTGAGTGTTTA 386 60.0
R: TGGGCAACAGAGCATGAC
BCRP11E Exon 11 F: CCACAACAATCCAAGACTGTG 423 60.0
R: GTAATCCTCCGGATCCCATC
BCRP12E Exon 12 F: GGTCTAGCCCTGAGGATGTG 403 64.7
R: GAGTGCAAAATGGACAGGTG
BCRP13E Exon 13 F: AGGGTGGTTGGAGAGTGGAT 412 60.0
R: AGCAGAGCCCCATTTACAGA
BCRP14E Exon 14 F: TGAGTGTCTTGAGTAAGTGGAGAGA 420 54.0
R: GACTCCCCAGCCTTGTGTTA
BCRP15E Exon 15 F: TCTTGATTGCCAGGGAAAAT 404 60.0
R: CGCGCACAACTCACTTTATG
BCRP16E Exon 16 F: TGACGGATGCTAGGAATGAA 430 64.7


R: CCCATGGTTACTGTCTGAGGA