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. 2014 Apr 21;9(4):e95751. doi: 10.1371/journal.pone.0095751

Table 2. Primers used for coding sequence amplification and qRT-PCR analysis.

TIGR gene ID Primer sequence (5′→3′)
Forward Reverse
LOC_Os05g01700 TGAGTCTGCGCTTCAAGAAA TATGCTCATCCCTGCAACTC
TAGCTGCAGTTGCAGAAGGA TTCGAGTTGCTGTTCTGTGG
LOC_Os05g01710 TCTGGAATTTGCTCGCGTTC AAACCCTGACCTCGCAGTTA
CTATGACGGAAGCCTTGGAG CAGGCCACAATCTTCACCTT
LOC_Os05g01730 TAGTGAGTGGTGAGAGGGGA AAAAGCCTACCCAAACTGCC
GCCCCTTCTGCTACATTGAG TGTGAGTGCTGAACCCTGAA
Actin GATTGCCAAGGCTGAGTACGA AAAAGAGAGAAACAAGCAGGAGGA

Note: For each putative gene, primers for coding sequence amplification are shown in the upper row; primers for qRT-PCR are shown in the lower row. The primers for Actin gene were used for qRT-PCR.