The cDNA fragments corresponding to Sw-5b (AY007366.1), NbHSP90 (Niben101Scf15166g03015.1), NbRAR1 (LC314308.1), NbEDS1 (Niben101Scf06720g01024.1), NbNDR1 (AY438029.1), NbNPR1 (Niben101Scf14780g01001.1), NbNRC2a (KT936525.1), NbNRC2b (KT936526.1), NbNRC3 (MK692736.1), NbNRC4 (MK692737.1), NbNRG1 (DQ054580.1), and NbADR1 (Niben101Scf02422g02015.1) were amplified by polymerase chain reaction (PCR) using PrimeSTAR High-Fidelity DNA Polymerase (TaKaRa, Dalian, China) and cloned into pTRV2 [37 (link)]. For constructing TRV-NbNRC2/3/4 and TRV-NbNRG1/NbADR1, gene fragments were fused by overlap PCR. The pTRV2-NbPDS, pTRV2-NbSGT1, and pTRV2-GUS vectors have been described previously [52 (link)].
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