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Table 2 Sequences of primers and probes of self-designed real-time RT-PCR gene assays

From: Preamplification techniques for real-time RT-PCR analyses of endomyocardial biopsies

Gene name

5' sense 3' primer sequence

5' antisense 3' primer sequence

TRBC

TCCGCTGTCAAGTCCAGTTCTA

GACAGGACCCCTTGCTGGTA

TRBV common antisense primer

 

CTGCTTCTGATGGCTCAAACA

TRBV2

ACTCTGAAGATCCGGTCCACAA

 

TRBV3

ATCAATTCCCTGGAGCTTGGT

 

TRBV4

CCTGAATGCCCCAACAGC

 

TRBV5

GCTCTGAGCTGAATGTGAACGC

 

TRBV5WBL

GCTCTGAGATGAATGTGAGTGC

 

TRBV6

CACTGACAAAGGAGAAGTCCC

 

TRBV6WBL6-2

AACTGCCAAAGGAGAGGTCCC

 

TRBV6WBL6-4

CACTGGCAAAGGAGAAGTCCC

 

TRBV7

CTCTCAGGTGTGATCCAATTTCG

 

TRBV7WBL7-2;7-3

AGCTCAGGTGTGATCCAATTTCA

 

TRBV7WBL7-9

CTTTCAGGTGTGATCCAATTTCT

 

TRBV9

CACAACAGTTCCCTGACTTGCA

 

TRBV10

CATGGGCTGAGGCTGATC

 

TRBV11

CTGCAGAGAGGCTCAAAGGAGTAG

 

TRBV12

AGAACCCAGGGACTCAGCTGT

 

TRBV13

GAACTGAACATGAGCTCCTTGGA

 

TRBV14

CTGAAAGGACTGGAGGGACGTAT

 

TRBV15

CAGGAGGCCGAACACTTCTTT

 

TRBV16

GCCTCCCAAATTCACCCTGTA

 

TRBV18

CCAGCATCCTGAGGATCCA

 

TRBV19

ACTGTGACATCGGCCCAAA

 

TRBV20

AACCATGCAAGCCTGACCTT

 

TRBV23

CCCTGCAGCCTGGCAAT

 

TRBV24

GCTAAATTCTCCCTGTCCCTAGAGT

 

TRBV25

TTCCCCTGACCCTGGAGTCT

 

TRBV27

GGCTTAAGGCAGATCTACTATTCAATG

 

TRBV28

GCCAGCACCAACCAGACAT

 

TRBV29

AGCCGCCCAAACCTAACATT

 

TRBV30

CGGCAGTTCATCCTGAGTTCT

 

HPRT-CCM

AGTCTGGCTTATATCCAACACTTCG

GACTTTGCTTTCCTTGGTCAGG

IL10

CAAGTTGTCCAGCTGCTTCAT

TTGGCGAAAGCAGCTCCTC

IFNγ

CAGGTCATTCAGATGTAGCGGATAA

AGGAGACAATTTGGCTCTGCATT

TGFβ

CCCTGCCCCTACATTGGAG

CCGGTTATGCTGGTTGTACA

FoxP3

TGGCAAACGGAGTCTGCAA

TCTCATCCAAGAGGTGATCTGCTT

T-bet

CAACACAGGAGGCGCACTGG

CCCCCTTGTTGTTTGTGAGCT

GATA3

CCTCATTAAGCCCAAGCGAAG

TTGGCATTTCCTCCAGAGT

GRAIL

GAAGCAGAGGCAATTAAAGGCAG

CATCAGGGCCAATTTCCTTGT

Granzyme A

CCCTGTGATTGGAATGAATATGGT

ACACCCTCGCACAACAAAGG

Granzyme B

GCGAATCTGACTTACGCCATTATT

CAAGAGGGCCTCCAGAGTCC

Granulysin

AAAACTGAAGAAGATGGTGGATAAGC

ATCGTGACCTCCCCGTCCTA

Perforin

GGACCAGTACAGCTTCAGCACTG

AGTCAGGGTGCAGCGGG

  1. Sequences of primers of self-designed real-time RT-PCR gene assays. For the different TRBV forward primers, one common reverse primer and one common MGB hybridization probe was designed. Wobbled (WBL) forward primers were used for TRBV5, 6 and 7.