Method for improving disease resistance by transforming arethusa with longan ferredoxin gene
A technology of gene transformation and disease resistance, applied in the field of genetic engineering
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[0021] Longan ferredoxin gene Dlfd3 , Dlfdc1 Design with restriction endonuclease sites Bgl II. Speech The corresponding primers upstream and downstream of I Dlfd3 F: 5'-GA AGATC TATGGCAACT GTGACCCTTAG-3', Dlfd3 R: 5'-GG ACTAGT GTAAAGTTCG CCTTCCTTGTG-3'; Dlfdc1 F: 5'-GA AGATCT ATGG CAACACTTCACTTCAG-3', Dlfdc1 R: 5'-GG ACTAGT ATCATCAGCA GTTGCCAGTTG-3'. 25μL PCR reaction system: 10 X PCR buffer ( plus Mg 2+ ) 2.5 μL, dNTPs ( 2.5 mmol L -1 ) 0.5 μL, forward primer (10 μmol L -1 ) 1 μL, reverse primer ( 10 μmol L -1 ) 1 μL, Taq ( 5 U μL -1 ) 0.2 μL, ddH 2 O 18.8 μL. PCR reaction program: pre-denaturation at 94°C for 4 min, denaturation at 94°C for 45 s, annealing at 54°C for 45 s, extension at 72°C for 40 s, 35 cycles, and finally extension at 72°C for 10 min. The PCR product was detected by 1.0% (W / V) agarose electrophoresis, and a band of about 500 bp was recovered, which was introduced into PMD18-T (TAKARA) to construct the PMD18-T plasmid. Using Fermen...
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