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Figures 2 and 3 show that the cell exposure to the chamber mixtures occurred directly after peak concentrations of the first-generation products were generated.
Generally, smaller and fewer products were generated by TAIL-PCR as compared to the corresponding reactions using FPNI-PCR.
No specific products were generated from digester sludge in PCR with the general pct primer or with the specific primers (pct-c1 to c7).
Daily products were generated for two representative days: 7 and 8 November 2003.
Similar to the IRC, the DC and FCB products were generated from a global network of solutions but post-processed.
IRC products were generated from a network of reference stations globally distributed, available in real-time and post-processed using final orbits and clocks.
When expressed in engineered E. coli cells synthesizing linear C30 carotenoids, polar carotenoid products were generated, identified as aldehyde and carboxylic acid C30 carotenoid derivatives.
PCR products were generated using specific primers, labeled with Cyanine 3 or Cyanine 5 fluorescent dyes, and hybridized overnight to the microarray.
PCR products were generated using primers listed in Table S1.
Two PCR products were generated to exclude the sequencing of a 7.5 kb first intron.
Briefly, PCR products were generated using primers into which restriction endonuclease sites were engineered (Table 1).
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