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. 2019 Aug 16;9(9):334. doi: 10.1007/s13205-019-1865-7

Table 1.

List of primers used in this investigation (sequence details, target region for amplification and the purpose oligonucleotides used are mentioned)

S. no. Primers Primer sequences (5′–3′) Viral genomic region Purpose
1 AC2-Ihp-F CATGCCATGGTCTAGAGT GGTATCCCCACCATCTTT AC2 ORF (transcriptional activator protein—TrAP) Generation of inverted repeats (RNAi vector)
2 AC2-Ihp-R CGGGCGCGCCGGATCCGA ACCTTGATTGACGGAGGA
5 qPCR-v-F ATGTGGGATCCATTGTTG AACG AV1 ORF (coat protein) MYMIV titre quantification
6 qPCR-v-R TCAATCTCCTCCGTGCAT TCG
7 q-AC2-RT-F GATTTTCGCACAGGGGAG TA AC2 ORF (transcriptional activator protein—TrAP) Quantification of MYMIV AC2 gene silencing
8 q-AC2-RT-R GCTTCAAGTCCAGGAAGCAC
9 F-CHSA ACTAACTTTGTGGAACTAAA Complementary to chalcone synthase intron in pFGC5941 PCR verification of inverted repeats (RNAi) vector construction