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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
1993-11-4
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pubmed:databankReference |
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pubmed:abstractText |
The polymerase chain reaction (PCR) was used to amplify approximately 1.5 kb segments of DNA containing complete Shiga-like toxin type II operons from Escherichia coli serotypes OX3:H21 and O111:H-. These fragments were cloned and DNA sequence analysis identified further variations compared with published SLT-II sequences.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0882-4010
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
77-82
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:8412629-Bacterial Toxins,
pubmed-meshheading:8412629-Base Sequence,
pubmed-meshheading:8412629-Cloning, Molecular,
pubmed-meshheading:8412629-DNA Primers,
pubmed-meshheading:8412629-Escherichia coli,
pubmed-meshheading:8412629-Genetic Variation,
pubmed-meshheading:8412629-Genome, Bacterial,
pubmed-meshheading:8412629-Molecular Sequence Data,
pubmed-meshheading:8412629-Operon,
pubmed-meshheading:8412629-Polymerase Chain Reaction,
pubmed-meshheading:8412629-Sequence Analysis, DNA,
pubmed-meshheading:8412629-Shiga Toxin 2
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pubmed:year |
1993
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pubmed:articleTitle |
Polymerase chain reaction amplification, cloning and sequencing of variant Escherichia coli Shiga-like toxin type II operons.
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pubmed:affiliation |
Department of Microbiology, Adelaide Children's Hospital, South Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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