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. Author manuscript; available in PMC: 2011 Sep 19.
Published in final edited form as: Biochem Biophys Res Commun. 2006 Sep 7;349(4):1250–1257. doi: 10.1016/j.bbrc.2006.08.166

Figure 1.

Figure 1

Agarose gel stained with ethidium bromide after electrophoresis. Lane 1, DNA ladder; Lanes 2-10, various plasmids digested with EcoR I and BamH I: lane 2, vector pLex5BA; lane 3, pLex5BA-fabD; lane 4, pLex5BA-fabI; lane 5, pLex5BA-murA; lane 6, pLex5BA-murG; lane 7, pLex5BA-prfB; lane 8, pLex5BA-rplJ; lane 9, pLex5BA-rpsL; lane 10, pLex5BA-trpS. Note, due to restriction sites and Shine-Delgarno sequences designed into PCR primers, the sizes of inserts shown in the gel are slightly bigger than the ORF sizes listed in Table 1.