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. 2011 May;55(5):1990–1996. doi: 10.1128/AAC.01688-10

Table 2.

Primers used for cloning and construction of ampG knockout mutants

Primer Sequence (5′–3′)a PCR product size (bp) Use
AGF1-ERI GATATAGAATTCCGGTCGCGGCGGCACCATCTG 823 ampG inactivation
AGR1-XbI TATATCTCTAGAGCTGGCGGGAGACTTGTAGGC
AGF2-XbI GATATATCTAGATACGTCACCGCGGTGATGGGC 621
AGR2-HD3 TATATCAAGCTTGTGCTGATCCTGCTGTTCCGC
AGF-ERI GATATAGAATTCAAGAAGGAGATATACATATGACTCAGCAATCCTGG 1,785 ampG cloning
AGR-HD3 TATATCAAGCTTTCAGTGCTGCTCGGCGTTCTGGTGTCCC
a

Restriction sites for endonucleases are underlined.