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. 2016 Jul 4;27(3):277–286. doi: 10.1007/s13337-016-0326-8

Table 1.

Details of the primers used for amplification of different components of CYVMV, CroYVMB, MCS cassette and GFP

Primer name Primer sequence (5′-3′) PCR template Location Nucleotide co-ordinates Amplicon size (kb)
BM90F ATGTCGAAGCGTCCAGCAGAT CYVMV genome V2 302-322 0.75
BM82R TACAGAATCGTAGAAGTAA Do V1 1045-1063
BM 638F CGACGCGTTGTGCGCAATACACTAC Do IR 122-141 1.70
BM 639R GGACTAGTTTAATAAAGATTGAATTTTATTG Do C3 1075-1094
BM 640RF GGTGTACAATTGAATTGGGGACACTCA Do IR 2613-2631 0.20
BM 641FR CCCAAGCTTTGTGCGCAATACACTACTTG Do IR 122-141
BM 652F ACTATCACCCTCAATCACTATAC Do C1 1944-1966 3.70
BM 653R AGAACGGGCAAGACGATG Do C1 1926-1943
BM 534F CARTCATATCCTCCTSYTTGAATTC CroYVMB Beta C1 312-336 0.26
BM 535R CATATATCAGAATGAGACGGGKTTG Do AT rich region 745-770
BM 642F ACGCGTGGACTAGTTTGCATGCCTGCAGGTCC pRI101 35S Promoter 9009-8991 1.30
BM 643R TGTACACCCAAGCTTCAGGAAACAGCTATGACCAT pRI101 NOS terminator 7701-7682
BM 650F CGGGGTACCGTAGATCTGACTAGTAAAGG pCAMBIA1302 GFP 4-23 0.77
BM 651F CGGAATTCGCTAGCTTTGTATAGTTCAT pCAMBIA1302 GFP 713-733
BM AC3F CAACCCCTATGTGTTTACAA CYVMV genome C3 1284-1303

Bold and italic indicate position of a restriction enzyme site