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. 2019 May 24;9:173. doi: 10.3389/fcimb.2019.00173

Table 2.

Primers used for PCR amplification and detection.

Primers Primers sequence (5-3) Amplification for
Mup-F AGGTCGACTCTAGAGGATCC
TAATTTTTCTGGCGCATTCAGC
Upstream border of mnmE
Mup-R CTCTTAAGTTTGCTTCTAAGAT
ATCTTTCTTTCTAA
AATTGTCTTATCTATTAGTG
Mdown-F TACGGGGAATTTGTATCGA
TGAACAAAAGTCATGT
Downstream border of mnmE
AAGAAAACTTGC
Mdown-R AAACGACGGCCAGTGAAT
TCTCTCTTGACCTGTTTG
GGTATTATAAA
Erm-F AATTTTAGAAAGAAAGATATC
TTAGAAGCAAACTTA
Ermr gene
AGAGTGTGTTGA
Erm-R TTCTTACATGACTTTTGTTCATCGA
TACAAATTCCCCGTAGG
MnmE-F CGGGATCCATGACACAC
ACATTTGCAGA
mnmE gene
MnmE-R CGCTCGAGTTAGTGACTGTCC
TTTGATTT
1453-F ATGGTTGTATTTATCAAATC
TAAAAAAGA
Upstream gene of mnmE
1453-R TTAAGCTACAGCAAATAGCTTTTCTT
1455-F GTGAAAGGCGGCATTCCC Downstream gene of mnmE
1455-R TCAGTCATTTACCCACACCCC
Test-F GACAAAATAGCTGGTGTAATAAAG Upstream to downstream regions of mnmE
Test-R CTGTGTATGAAGGAGTTGAGGC
CM-F GATTCTGCAGTTTCGACGTCCTTTATC mnmE gene and its
CM-R CTCGGATCCTTATTTTCCAAGACAGA Promoter