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. 2015 Nov 5;2015:630287. doi: 10.1155/2015/630287

Table 1.

Primer pairs used for cloning, qRT-PCR, detection of transgene, and conventional RT-PCR.

Protein Sequence (5′-3′) Amplicon length (bp)
Cloning of AMHR2-CD
AMHR2-CD
 Forward GGATCCAAGGCCTGCAGAGTGCAAGGTG 1209
 Reverse AAGCTTCTACTCATTTACATACACCTG
TgMISIIR-TAg transgene expression
SV40-TAg
 Forward TGCATGGTGTACAACATTCC 773
 Reverse TTGGGACTGTGAATCAATGCC
qRT-PCR
IFNγ
 Forward GGATATCTGGAGGAACTGGCAA 110
 Reverse TGATGGCCTGATTGTCTTTCAA
TNFα
 Forward CGAGTGACAAGCCTGTAGCC 209
 Reverse GTGGGTGAGGAGCACGTAGT
IL-2
 Forward GCAGGCCACAGAATTGAAAG 207
 Reverse TCCACCACAGTTGCTGACTC
CD4
 Forward ACACACCTGTGCAAGAAGCA 69
 Reverse GCTCTTGTTGGTTGGGAATC
CD8
 Forward TTACATCTGGGCACCCTTG 132
 Reverse TTGCCTTCCTGTCTGACTAGC
NKR-P1A
 Forward GGCTTGGCATGAGTCACC 75
 Reverse TTCAGAGCCAACCTGTGTGA
β-actin
 Forward GGTCATCACTATTGGCAACG 133
 Reverse ACGGATGTCAACGTCACACT
Conventional RT-PCR
AMHR2
 Forward GTATCCGCTGCCTCTACAGC 193
 Reverse CAGAAGTCAGTGCCACAGGA
β-actin
 Forward GGTCATCACTATTGGCAACG 133
 Reverse ACGGATGTCAACGTCACACT