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. 2014 Dec 18;9(3):795–800. doi: 10.3892/etm.2014.2148

Table I.

Primers used in the study.

Procedure Primers Primer sequences (5′-3′)
ChrT gene fragment Scfmn1-F GATGTGCAACAAGACGAAGGT
Scfmn1-R GATGACTCCGCCCATAAACTC
5′-hiTAIL-PCR Scfmn-SP1 GATGACTCCGCCCATAAACTCC
Scfmn-SP2 AGACTCACCAGAGTCGATGGCGTTTTTCAGGC
Scfmn-SP3 CTATCACAACCCCATCCGCCT
Scfmn-AD1 ACGCTAGACTCACCTCVNVNNNGGAA
Scfmn-AC1 ACGCTAGACTCACCTC
3′-hiTAIL-PCR Scfmn-SP1′ AGGCGGATGGGGTTGTGATAG
Scfmn-SP2′ GAACTGCACACGCCTGAAAAACGCCATCGACT
Scfmn-SP3′ GTGCGCGCTGCCAGTATCAT
Scfmn-AD1′ ACGATGAACTGCACTGVVNVNNNCCAA
Scfmn-AC1′ ACGATGAACTGCACTG
Full-length ChrT gene Scfmn-F ATCATGTCAGATACCTTGAAAGTGG
Scfmn-R TGCTTTAACCCGCCGAATATA

PCR, polymerase chain reaction; F, forward; R, reverse; hiTAIL-PCR, high efficiency TAIL-PCR.