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. 2017 Feb 15;15(4):1555–1564. doi: 10.3892/mmr.2017.6206

Table III.

Primers for amplifying TCRβ∆IgC-EYFP and TCRα∆IgC-ECFP fusion genes (regular polymerase chain reaction (PCR) and SOE-PCR).

Gene name Primer name Direction Primer sequence
TRBV P1 Forward ATAGCTAGCGCCACCATGGGCTGCAGGCTGCTCTG
P2 Reverse ACATCTGCATCAAGTTGTTTCTCCAGTACGGTCAGCCT
TRGC P3 Forward AGGCTGACCGTACTGGAGAAACAACTTGATGCAGATGT
P4 Reverse CGGAGGTGAAGCCACAGTCTGTCTTTATTGGAGGAAAG
TRBCm P5 Forward CTTTCCTCCAATAAAGACAGACTGTGGCTTCACCTCCG
P6 Reverse CTCGCCCTTGCTCACCATGCCTCTGGAATCCTTTCT
EYFP P7 Forward AGAAAGGATTCCAGAGGCATGGTGAGCAAGGGCGAG
P8 Reverse CGGCGTCGACTTACTTGTACAGCTCGTC
TRAV X1 Forward ACGCCACAACCTTGGCCACCATGATATCCTTGAGAGTT
X2 Reverse GGTTTGGTATGAGGCTGACTATTTGGTTTTACTGTCAGTCTGG
TRDC X3 Forward CCAGACTGACAGTAAAACCAAATAGTCAGCCTCATACCAAACC
X4 Reverse GCTTGACATCACAGGAACTTTCTGTAGAATCTGTCTTCACTTC
TRACm X5 Forward GAAGTGAAGACAGATTCTACAGAAAGTTCCTGTGATGTCAAGC
X6 Reverse CTCCTCGCCCTTGCTCACCATGCTGGACCACAGCCGCAGC
ECFP X7 Forward GCTGCGGCTGTGGTCCAGCATGGTGAGCAAGGGCGAGGAG
X8 Reverse AGTGCGGCCGCTTACTTGTACAGCTCGTCCAT

Restriction enzyme sites are underlined. SOE-PCR, splicing by overlap extension-polymerase chain reaction.