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. 2019 Feb 17;20(4):866. doi: 10.3390/ijms20040866

Table 3.

Primers for QTL fine mapping, quantitative real-time polymerase chain reaction (qRT-PCR), vector construction, and gene editing.

Primer Forward (5′-3′) Reverse (5′-3′) Experiment
RM3700 AAATGCCCCATGCACAAC TTGTCAGATTGTCACCAGGG Fine mapping
C9-1594 CCTGTACACTGTAGGCCTGT GGTGTCAAAGTACATAGGCCC
C9-1635 GGTGGAAAGGAAGGAGAGCT CTAGCCCTGCCTCGTTGTAA
C9-1638 GTGTGTGTGTGTGTGTGTGT TCATAGTACATGCCCTCCGT
C9-1640 ATAAGTCCATATTGCCCACCTC AAGCTTCTGGATCGTTAACAGG
C9-1642 GTACCCTCCTCCGATGACAC TTGTGGAGGACGAGAAGGTG
C9-1715 GGTGGCGAGAAGAATTTGCA TTTCGCCTCTCACTGACCTT
B9-11 TCTTACGAATAGGCCCTTGG AGAGCCCACAACACTTGTGC
Actin ATCCATCTTGGCATCTCTCAGC CACAATGGATGGGCCAGACT qRT-PCR
LOC_Os09g26960 CTGAGCCTCGCCAATCTG CGAAGATCTCCTCCATGCTC
LOC_Os09g26970 CAAACATCTGGGCTTGGTCT TCTAAGCAACCTGCCCAATC
LOC_Os09g26980 ATTGATGTGAAAGGGCAAGACT CACCTTAAGCCCAAGGTTGTAG
LOC_Os09g26999 GTAGCTGCAAGCCAAGCTG TTGAAGCAGCTGGAGCAAC
POs26999 GGCCAGTGCCAAGCTTAAGGGAAGTTGGCCGCCTGCC AGGGTCTTGCAGATCTCTCCACACGCAGCACGCCAAC Vector construction
Os09g26999-g++/g-- GGCAGGTGGTGATGGAGGCGCCG AAACCGGCGCCTCCATCACCACC
Os09g26999-JC CGGCGATTTATACCCACCAC CGCTCACCTTGAGGAACGT Detection of target mutations
Hyg-F1 GCTGTTATGCGGCCATTGTC GACGTCTGTCGAGAAGTTTC
Cas9-F2/pC1300-R2 ACCAGACACGAGACGACTAA ATCGGTGCGGGCCTCTTC
T3 ATCGGTGCGGGCCTCTTC