Table 1.
Oligo | 5′–3′ sequence (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).