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. 2016 Apr 29;17(5):628. doi: 10.3390/ijms17050628

Table 1.

Oligonucleotide primers for PCR used in this study.

Names Primer Sequences (5′-3′) Positions
MBOV_RS02825
580F1 CGGGGTACCGAAAATGGCACAATTAAG 79→97
580R1 AGTTTTTTCTCCCAGCCATCTACTAACTC 316←345
580F2 GTTAGTAGATGGCTGGGAGAAAAAACTTAG 317→347
580R2 AATATTTAGCCTTCAATTTGTCCCAATCTATG 437←469
580F3 CTAAATATTTTGATGCAGAAATAGTTAAATGGAGCG 460→496
580R3 GGCATAATGCTCCCAGTAAACTGGATTTTT 855←885
580F4 AATCCAGTTTACTGGGAGCATTATGCC 855→885
580R4 TAAATGTTAGATTGAATCCAGTATGGC 956←983
580F5 GCCATACTGGATTCAATCTAACATTTA 956→983
580R5 AGTGTTTATCTAGCAATGTCCATTTTC 1000←1027
580F6 TGGAAAATGGACATTGCTAGATAAACA 998→1025
580R6 CGCGGATCCTTATTTATTTTTGTATGAATC 1071←1092
MBOV_RS02825ΔTNASE_3
580F1 CGGGGTACCGAAAATGGCACAATTAAG 79→97
580UR TGGCAATGCAAATTTAGCCTTCAATTT 530←543, 1027←1040
580DF AAATTGAAGGCTAAATTTGCATTGCCA 530→543, 1027→1040
580R6 CGCGGATCCTTATTTATTTTTGTATGAATC 1071←1092

The underlined sequences were sites for restrictive digestion. The bold indicates TGA to TGG change to permit tryptophan expression in E. coli. The arrows showed nucleotide position within MBOV_RS02825 coding open reading frame (ORF).