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. 2006 Sep 29;188(23):8013–8021. doi: 10.1128/JB.01160-06

FIG. 3.

FIG. 3.

RT-PCR analysis of the algT-mucABD gene cluster in P. syringae pv. glycinea. (A) Agarose gel with PCR products obtained from PG4180.muc cDNA (R) and PG4180.muc genomic DNA (C) as a positive control. For size estimation, a DNA size standard (M) was included. Numbers 1 to 9 represent the PCR products obtained by different primer combinations as described in panel B. (B) Schematic overview of length and location of the PCR products (1 to 9) within the algT-mucABD gene cluster. A solid arrow indicates that a PCR product was obtained from PG4180.muc cDNA, whereas a dashed arrow indicates that no PCR product could be obtained.