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. 2016 Apr 19;6:44. doi: 10.3389/fcimb.2016.00044

Table 2.

Primers used for PCR amplification and detection.

Primers Primers sequence (5′−3′)a Amplification for
Gup-F CTTCAAGCTTGCTTTTGTGGACTTA Upstream border of gidA
Gup-R GTTTGTCGACTCATGTTGTTCTCTCCT
Gdown-F GATCCCGGGGGCTGTTCTTTTCGC Downstream border of gidA
Gdown-R CCCCGAATTCTTCCTTGACCACAACC
Erm-F GTCTGGATCCCTTAGAAGCAAACTTAA Erm r gene
Erm-R GTTAGGATCCATCGATACAAATTCCCCG
GidA-F CGGGATCCATGACACACACATTTGCAGA gidA gene
GidA-R CGCTCGAGTTAGTGACTGTCCTTTGATTT
2162-F GTGATGAAAAGATTTCGATT Downstream gene of gidA
2162-R TTATCCAAAGTCAAGCCA
2164-F GGTTGATTATAAAAGATGG Upstream gene of gidA
2164-R TCATGTTGTTCTCTCCTT
a

Underlined nucleotides denote enzyme restriction sites.