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

Table V.

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

Gene Primer name Direction Primer sequence
TRBV P1 Forward ATAGCTAGCGCCACCATGGGCTGCAGGCTGCTCTG
P2 Reverse ACATCTGCATCAAGTTGTTTCTCCAGTACGGTCAGCCT
TRGC+GCm P3 Forward AGGCTGACCGTACTGGAGAAACAACTTGATGCAGATGT
O4 Reverse CCTCGCCCTTGCTCACCATTGATTTCTCTCCATTGCAG
EYFP O5 Forward CTGCAATGGAGAGAAATCAATGGTGAGCAAGGGC
P8 Reverse CGGCGTCGACTTACTTGTACAGCTCGTC
TRAV X1 Forward ACGCCACAACCTTGGCCACCATGATATCCTTGAGAGTT
X2 Reverse GGTTTGGTATGAGGCTGACTATTTGGTTTTACTGTCAGTCTGG
TRDC+DCm X3 Forward CCAGACTGACAGTAAAACCAAATAGTCAGCCTCATACCAAACC
H4 Reverse CCTCGCCCTTGCTCACCATCAAGAAAAATAACTTGGCAGT
ECFP H5 Forward ACTGCCAAGTTATTTTTCTTGATGGTGAGCAAGGGCGAGG
X8 Reverse AGTGCGGCCGCTTACTTGTACAGCTCGTCCAT

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