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Detection of enterotoxigenic Escherichia coli after polymerase chain reaction amplification with a thermostable DNA polymerase.

The direct identification of enterotoxigenic Escherichia coli from clinical specimens was examined by using the polymerase chain reaction (PCR) for amplifying the heat-labile toxin (LT) gene. Two synthetic primers, each of which was 20 bases in length, were used with the thermostable DNA polymerase...

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Dettagli Bibliografici
Autore principale: Olive, D M
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1989
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC267288/
https://ncbi.nlm.nih.gov/pubmed/2644292
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