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. 2015 Jul 2;10(7):e0127670. doi: 10.1371/journal.pone.0127670

Table 2. Primer information used for cloning the bovine HIBADH gene promoter region.

Primer names Sequences (5′-3′) Annealing temperature (℃) The size of production (bp)
Q-1 F:GCTACCATGCCAAGAACCCT 62.5 1430
R:TGCTAGGAACTTGCTCCTCAA
Q-2 F:ACACACAAACATACTTTCTGCACT 59.7 1675
R: GGCCCTCCAATTGTCCTCAA
Q-3 F:TGTTTTGGGTGTCCATGGCT 61.1 1812
R:GGCCCTCCAATTGTCCTCAA
P-1 F:CGGGGTACCGTCAAAGAAAGGAACTGCT 61.9 2340
R:CCGCTCGAGAATGATACGGAAGGTGGAA
P-2 F:CGGGGTACCAGTCAGCTTCTCGAACCAGA 61.6 1805
R:CCGCTCGAGAATGATACGGAAGGTGGAA
P-3 F:CGGGGTACCAGAATCTATTCGGCAAATTA 63.2 1495
R:CCGCTCGAGAATGATACGGAAGGTGGAA
P-4 F:CGGGGTACCAGGCGCTGCGATTAGA 60.1 618
R:CCGCTCGAGAATGATACGGAAGGTGGAA
G F:CTCCAACATCACAGTTCAAAAG 62.5 967
R:TACCCGCTGCAAGGCT
M-outer F:ATTTGGGATTTTTGATTGATTTTT 52.2 218
R:CTCACCCACTAACTAACAAAATAC
M-inner F:GGGGTTTGTAAGGTGAT 52.2 175
R:GGCGGTAACAAAATACGTAATA
PT F:GCATGGCAGCCTCCTTACG 61.2 1254
R:AGAGACCATCAGTGGCTTGC

Note: The Kpn I sites (CGGGGTACC) were added to the forward primers (P-1, P-2, P-3, and P-4) as recognition and protection sites. The reverse primers (P-1, P-2, P-3, and P-4) (3′) contained the Xho I sites (CCGCTCGAG).