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. 2022 Jul 22;11(8):1092. doi: 10.3390/biology11081092

Table 1.

PCR primers used in the study.

Primer Name Sequence(5′-3′) Usage
GSX7-2097F GGTTACATATGTTTATTACTAAGC Full-length cloning of forward promoter
GSX7-2097R GGGTTTGAGGCGACCGGCGACCGGC
GSX7R-2097F GGGTTTGAGGCGACCGGCGACCGGC Full length cloning of reverse promoter
GSX7R3R GGTTACATATGTTTATTACTAAGCA
GSX7R-1765F ATGGCGCATGATTATATTCCGATTA 5′ deletion cloning
GSX7R3R GGTTACATATGTTTATTACTAAGCA
GSX7R-1198F GTCTCCGTGGGCTGCGCTAGCTTGC 5′ deletion cloning
GSX7R3R GGTTACATATGTTTATTACTAAGCA
GSX7R-554F ACTTGTACTTAGAAAATAACATGTT 5′ deletion cloning
GSX7R3R GGTTACATATGTTTATTACTAAGCA
GSX7R-2097F GGGTTTGAGGCGACCGGCGACCGGC 3′ deletion cloning
GSX7R-1543R GGAGATAGACATTATTTGGAAATGA
GSX7R-2097F GGGTTTGAGGCGACCGGCGACCGGC 3′ deletion cloning
GSX7R-1212R CGCGCCTGCCGTTGCCGCCGGTCCT
hptF ACACAGCCATCGGTCCAGA hpt maker gene identification
hptR TAGGAGGGCGTGGATATGTC
Os8GSX7F GCTCGACGCATGCATGGCACAG RT-PCR
Os8GSX7R GTCCAATATGTGGAATCTGATC
GUSF GAACTGGCAGACTATCCCGCCGG RT-PCR
GUSR CCTGCCAGTCAACAGACGCGTGG
ActinF CATGCTATCCCTCGTCTCG Reference gene
ActinR CGCACTTCATGATGGAGTTG