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. 2015 Dec 7;8:36. doi: 10.1186/s12284-015-0070-5

Table 1.

Specific primers used in this study

Primer name Sequence (5′ to 3′) Target gene
Hygromycin-F GACCTGATGCAGCTCTCGGAG hptII
Hygromycin-R TGCTCCATACAAGCCAACCACG
GUS-F AAAAAACTCGACGGCCTGTGGG GUS
GUS-R GCATCTTCATGACGACCAAAGC
Ubiquitin pro.-F CTGATGCATATACAGAGATGC a CX3 or CX5
Nos ter.-R TGACAGCTTATCATCGGATC
CKX2-F GTCCACGACGGCGAGCTCAA OsCKX2
CKX2-R TCCATCTTGGCATCTCTCAG
Actin-F GGTAATGTGTTGGACTCTGG Actin
Actin-R GCAGTGATCTTCCTTGCTCA
3′UTR-F CGGTGACGAGGTGTTCTACAC OsCKX2 3′ UTR
3′UTR -R CCAAGATCTCGTCGTTCTGC
rRNA-F GATAACTCGACGGATCGCACGG 17S rRNA
rRNA-R GCCTGCTGCCTTCCTTGGATGTG
OsCKX1-F GCACCCGTGGCTCAACCTG CKX1
OsCKX1-R GATGTCGGTGGCCGTCTGG
OsCKX3-F TTTCTTATGCTGATGTGGGTG CKX3
OsCKX3-R GAACATTGCTAATCTGAGGTCC
OsSPL14-F TGAATTTGACCAAGGAAAAC SPL14
OsSPL14-R ATCCAACGTAAAGCTTCTGA
D53-F CCAAGCAGTTTGAAGCGAC D53
D53-R CCGCAAGTTTATCAAAGTCAA
OsTB1-F CAAGAAATCTCGGCGGCTAG TB1
OsTB1-R CGAATTGGCGTAGACGAC

ashRNA cannot be amplified directly by PCR. Thus, a 867 bp fragment containing partial promoter, shRNA and partial terminator were amplified for detecting the CX3 or CX5 gene