DNA amplification to enhance detection of genetically engineered bacteria in environmental samples.
The polymerase chain reaction (PCR) was performed to amplify a 1.0-kilobase (kb) probe-specific region of DNA from the herbicide-degrading bacterium Pseudomonas cepacia AC1100 in order to increase the sensitivity of detecting the organism by dot-blot analysis. The 1.0-kb region was an integral porti...
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| Pubblicato in: | Appl Environ Microbiol |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society for Microbiology (ASM)
1988
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC202834/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3190225/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/aem.54.9.2185-2191.1988 |
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