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. 2020 Nov 18;26(11):2189–2197. doi: 10.1007/s12298-020-00910-2

Table 1.

The primers used in the study

Primer name Sequence (5′-3′) Description
qPf GGGAGGACGAGAAGGAAAGG qRT-PCR of ZmPP2C26 gene
qPr AACTGCACGATCACGACACT
qGf TGAATGGCAAGCTCACTGGT qRT-PCR of ZmGAPDH gene
qGr TGAATGGCAAGCTCACTGGT
PF0 TCACTTTACCATTTTTATGCGGGA Forward primer for P2175 amplification
PR CGGGGCTAGGGTTTTTTTTTCTTTC Reverse primer for P2175 amplification
gus-PF0 acgacggccagtgccaagcttTCACTTTACCATTTTTATGCGGGA Forward primers for PCR of r promoter::GUS construct
gus-PF1 acgacggccagtgccaagcttGAGCAAATCGACTCCATCCTT
gus-PF2 acgacggccagtgccaagcttAGCGTCGCGTCTATCCTTCTC
gus-PF3 acgacggccagtgccaagcttCTACGAAACCGCAAAGTCCAT
gus-PR tgtgattgtgatgtatctagaCGGGGCTAGGGTTTTTTTTTCTTTC Reverse primer for PCR of promoter::GUS construct
luc- PF0 ctatagggcgaattgggtacc TCACTTTACCATTTTTATGCGGGA Forward primers for PCR of promoter::LUC construct
luc- PF1 ctatagggcgaattgggtaccGAGCAAATCGACTCCATCCTT
luc- PF2 ctatagggcgaattgggtaccAGCGTCGCGTCTATCCTTCTC
luc- PF3 ctatagggcgaattgggtaccCTACGAAACCGCAAAGTCCAT
luc- PR caggaattcgatatcaagcttCGGGGCTAGGGTTTTTTTTT Reverse primer for PCR of promoter::LUC construct