Figure 3.

Construction of transcription plasmids, pRG147and pRG198. The plasmids were constructed by cloning PCR-amplified E. chaffeensis-specific promoters of p28-Omp14 (pRG147) and p28-Omp19 (pRG198) into the EcoRV located upstream of a G-less cassette in pMT504 [26].

Faburay et al. BMC Microbiology 2011 11:83   doi:10.1186/1471-2180-11-83
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