Skip to main content
. 2014 Feb 21;25(2):166–177. doi: 10.1089/hgtb.2013.212

Table 1.

Oligonucleotides Used in This Study

Oligo 5–3sequence (restriction sites underlined) Restriction site
P1 GCGGCGGCCGCCACCATGGTGATTCTTCAGCAGGGGGAC NotI
P2 GCGGCTAGCGAAGTTCCGCAGGTACTTGAC NheI
P3 GCGCTTAAGCAGGTCTAACTTTCTGAAGCTG AflII
P4 GCGGGTACCTCACTTGCCGCTCCTGGAGCC KpnI
P5 GGCACCTAGTGGCTTTGAGGTAAGTATCAAGGTTACAAGAC  
P6 GCGGCTAGCTCAGAAACGCAAGAGTCTTC NheI
P7 CTTCTTTGTGCGATGCATCAAG NsiI
P8 GCGCTTAAGCGACGCATGCTCGCGATAG AflII
P9 CGCCCTCGCTCCAGGTCCTGTGGAGAGAAAGGCAAAG  
P10 GAACCCGAACCGGTCCTTG AgeI
P11 GCGGCTAGCCCCCGGGTGCGCGGCG NheI
P12 GCGGTCGACGAAACGGTCCAGGCTATGTG SalI
P13 GCGGCGGCCGCCCCCGGGTGCGCGGCG NotI
P14 GCGCTTAAGGAAACGGTCCAGGCTATGTG AflII
P15 CAGGCACCTAGTGGCTTTGAGGTACCAGGCTAGGGACAGG  
P16 GCGGCTAGCCGCCTGAGCCCAGAAGTTC NheI
P17 CGCCCTCGCTCCAGGTCCTGAAGGAGACAAGAGGTATG  
P18 GCGCTTAAGCACCGCTTGTGTTGATCCTC AflII
P19 GCCAGGGAAGGATCCCATG BamHI
P20 GCGGGTACCTCATGCGTAATCCGGTACATCGTAAGGGTACTTGCCGCTCCTGGAGCC KpnI
P21 AGCTTCGTAGAGTTTGTGGAGCGG  
P22 GAGGGGCAAACAACAGATG  

Oligonucleotides were used to make 5′ and 3′ vectors of the dual-vector platforms (P1–P20). Oligonucleotides were used to characterize the fidelity of the overlap in simple overlap, trans-splicing and AP hybrid vector platforms (P21–P22). Restriction sites used for cloning are underlined and the introduced HA tag is noted in italics (P19).