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Table 1 Oligonucleotide primer sequences used for PCR in this study

From: Molecular characterization of Babesia microti thioredoxin (BmTrx2) and its expression patterns induced by antiprotozoal drugs

Name

Sequence (5'-3')

Description

BmTrx2-Con-F

GCACTACACATACCCACGTATTAT

Forward primer specific for BmTrx2 conserved sequence (partial)

BmTrx2-Con-R

TGCGTCAATTCCAGTGACAATTAC

Reverse primer specific for BmTrx2 conserved sequence (partial)

3' GSP1

CATAGAGACAGTGGATTGCTACAGG

Forward gene specific primer for 3'-end of BmTrx2 in primary PCR

3' GSP2

GAGCACAGAGTTACTACGATTCCCAT

Forward gene specific primer for 3'-end of BmTrx2 in second PCR

5' GSP1

CCGATTCCAACTTAGG

Gene specific primer for reverse transcription of B. microti mRNA

5' GSP2

GGGAATCGTAGTAACTCTGTGCTCC

Reverse gene specific primer for 5'-end of BmTrx2 in primary PCR

5' GSP3

GCCTTCCTGTAGCAATCCACTGTC

Reverse gene specific primer for 5'-end of BmTrx2 in second PCR

BmTrx2-ORF-F

CATATGCATAGCATGAGTAGGGTCATATTT

Forward primer containing an NdeI site for cloning into pET30a(+)-BmTrx2

BmTrx2-ORF-R

CTCGAGCTTTTGAGGGGGTGTGACGTGT

Reverse primer containing a XhoI site for cloning into pET30a(+)-BmTrx2

BmTrx2-qRT-F

GTCTAGTGGCGTTGTTGTTGC

Forward gene specific primer for the quantification of BmTrx2 mRNA

BmTrx2-qRT-R

GACCGATTTCATCTGATTGCTTA

Reverse gene specific primer for the quantification of BmTrx2 mRNA

Bm18S-qRT-F

GTTATAGTTTATTTGATGTTCGTTT

Forward gene specific primer for the quantification of B. microti 18S mRNA

Bm18S-qRT-R

AAGCCATGCGATTCGCTAAT

Reverse gene specific primer for the quantification of B. microti 18S mRNA