Optimization of RNA extraction for PCR quantification of aromatic compound degradation genes.
Ontology highlight
ABSTRACT: Seven different bacterial strains and primer sets and a mixed community were used to evaluate the use of reverse transcriptase quantitative PCR (Q-PCR) and Q-PCR of oxygenase genes to assess various approaches for monitoring the bioremediation of polluted sites. Differences in maximum activity were seen when different RNA extraction kits were compared.
SUBMITTER: Kong W
PROVIDER: S-EPMC2820950 | biostudies-literature |
REPOSITORIES: biostudies-literature
ACCESS DATA