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. 2013 Feb 14;304(8):G741–G748. doi: 10.1152/ajpgi.00018.2013

Table 1.

Combination of primers used to amplify the respective genes by real-time PCR, semiquantitative PCR, and cloning of the promoters

Primers (5′-3′)
Gene Forward Reverse
PCR primers
hRFVT-1 AAAAGACCTTCCAGAGGGTTG AGCACCTGTACCACCTGGAT
hRFVT-3 CCTTTCCGAAGTGCCCATC AGAAGGTGGTGAGGTAGTAGG
Human β-actin AGCCAGACCGTCTCCTTGTA TAGAGAGGGCCCACCACAC
rRFVT-1 AGCTACCTGTAGTGGTGA CTCAGCCCCTGAACCA
rRFVT-3 TAAGGAAGATCACGGGCACCTC GTCATCCAACTGGCCAACACAG
18S GGGAGGTAGTGACGAAAAATAACAAT TTGCCCTCCAATGGATCCTC
hnRNA primers
hRFVT-1 GACCTGCCTGTGAC AACCCTCTGGAAGG
hRFVT-3 TGACATCGCACAGG CCTGCTGTTGATCTG
Human β-actin TTCCTGGGTGAGTGGAG GGACTCCATGCCTGAGAG
rRFVT-1 CTTTAGGCCAGCTTCTTG AAAATGCGAGTGGACAG
rRFVT-3 TGGTGTTCTGCCCTCAG GGGCCTGTGTTTGTAGC
Rat β-actin CTGCTCTTTCCCAGATGAG CTCATAGATGGGCACAGTG
Primers used for cloning of hRFVT-3 promoter
hRFVT-3 CGACGCGTTTGATCAAATCCTGGTTG CCGCTCGAGCTTCTTCCTTCTAGTACAAAGC

hRFVT and rRFVT, human and rat riboflavin (RF) transporters, respectively; hnRNA, heterogeneous nuclear RNA.