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. 2009 Feb 23;587(Pt 10):2211–2224. doi: 10.1113/jphysiol.2008.159087

Table 1.

Bestrophin and control primer sequences used in the RT-PCR amplification reactions

Gene Sense (5′–3′) Antisense (5′–3′) Expected product size (bp) GenBank accession
hBest1 5′ 304-GTATTGCGACAGCTACATCCAG-327 794-ATCCAGTCGTAGGCATACAGGT-771 488 NM 004183
hBest1 mid 771-ACCTGTATGCCTACGACTGGAT-794 1233-CTGGAACTCCATCTCCTCTTTG-1210 460 NM 004183
hBest1 3′ 1105-GGACATGTACTGGAATAAGCCC-1128 1514-GTGTCTGGGGCACTGTAGTC-1493 407 NM 004183
hBest2 443-AGTTTGAAAACCTGAACTCATCCTA-469 865-AGAAAGTTGGTCTCAAAGTCATCAT-839 420 NM 017682
hBest3 833-ACAAGTGACAGCTCCATGTTCTTAC-859 1350-TTTTAGAAAGGTATCACCAGGGTCT-1324 515 NM 032735
hBest4 957-TTTGAGACAAATCAGCTCATAGACC-983 1568-TCTTCTCTTTCAAGTTCTGTCCCTA-1544 609 NM 153274
β-Actin 260-GCATCCTCACCCTGAAGTAC-281 717-TTCTCCTTAATGTCACGCAC-697 455 NM 001101
GAPDH 627-ACCACAGTCCATGCCATCAC-648 1080-TCCACCACCCTGTTGCTGTA-1059 451 NM 002046

PCR primers for hBest1, 2, 3, 4, β-actin and GAPDH that have been used in this study. Primers were designed using the OligoPerfect™ primer design programme by Invitrogen.