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. 2005 Jul;187(13):4505–4513. doi: 10.1128/JB.187.13.4505-4513.2005

FIG. 3.

FIG. 3.

RT-PCR (A) and Northern blot (B) analyses of omcF expression. Total RNA was extracted from acetate-fumarate or acetate-Fe(III) citrate-grown wild-type cultures. (A) The following primers were used for cDNA synthesis: lane 2, none; lane 3, omcF-specific primers RT4017F and RT4017R (Table 1); lane 4, random hexamers; lane 5, random hexamers. (B) The Northern blot was hybridized with 32P-labeled probes specific for omcF as indicated. Equal amounts of mRNA (20 μg/lane) were loaded. (C) Ethidium bromide-stained gel showing the positions of 16S and 23S rRNA, as a loading control.