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. 2019 Feb 25;9:2702. doi: 10.1038/s41598-019-38570-2

Table 3.

Primer sets used for cloning and qRT-PCR of TaGW8-B1 gene in this study.

Primer Primer sequence (5′-3′) Annealing Temp. (°C) Size of PCR fragment (bp)
TaGW8-P1 Forward: CCAACACACAAGCTCCAGAC
Reverse: GCAACACATGAACAGCCACT
58 1433
TaGW8-P2 Forward: GAATGAGAGGGACAGGGGAG
Reverse: TCATGAATGGGGCCAGGATT
57 1151
TaGW8-P3 Forward: TCTCTTCGCTCATCCATTCCT
Reverse: GCTATCCCCACAACATAGACC
54 1297
TaGW8-P4 Forward: ATGCAGTGTGGACTTTGTGG
Reverse: TTGCGATGCCAGTTGAACAT
57 1149
TaGW8-P5 Forward: TCCTCTACTCGGAACCTGAA
Reverse: GTGCCCATCAAGACGCTTTC
55 1235
TaGW8-P6 Forward: TGTCTAACTACCTAGGAGCATCT
Reverse: TGTGAAGAAGGTAAAGAGTGGC
61 1073
TaGW8-P7 Forward: CTTGCAGCTTGTAACCCACC
Reverse: GAACGTCGGTGCTCTGAAAT
61 1498
GW8-7B Forward: CGCTCATCCATTCCTTCATCG
Reverse: GCTATATGGGTTGGTGTCGC
60 1097/1373
TaGW8-P8 Forward: TTCTCTGATGGGCTGACTCC
Reverse: TGGGGATGTGTTCAGTCTGT
60 121
β-actin gene primer Forward: GTGTCGCACCAGAGGATCAT
Reverse: CGCTGGCATACAAGGACAGA
60 153