
In Situ-Synthesized Virulence and Marker Gene Biochip for Detection of Bacterial Pathogens in Water
Appl. Environ. Microbiol. Miller et al.
74: 2200
Supplemental material
Files in this Data Supplement:
- Supplemental file 1
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Image of gel electrophoresis bands observed after split multiplex PCR (Fig. S1); justification of the binning approach used to establish the relationship between Δ G 0 Duplex and the success of probe design (Fig. S2); effect of window size used for binning of the probes on the relationship between Δ G 0 Duplex and the success of probe design (Fig. S3); effect of window size used for binning of the probes on the relationship between ƒ´G0duplex and probe selectivity (Fig. S4); primer sequences used in this study along with amplicon lengths (Table S1); design of the split multiplex PCR described (Table S2); Excel document containing probe sequences of targeted and nontargeted probes; raw hybridization data in Excel format.
8 MS Excel files and 1 MS Word document Zipped, 3.4MB