Show simple item record

dc.contributor.advisorGouws, P.A
dc.contributor.authorDavids, R
dc.date.accessioned2023-06-12T17:16:42Z
dc.date.available2023-06-12T17:16:42Z
dc.date.issued2002
dc.identifier.urihttp://hdl.handle.net/11394/10170
dc.descriptionDoctor Educationisen_US
dc.description.abstractThe nucleotide primer pair, Redl and Red2, was designed from the nucleotide sequence obtained from the NCBI database (Fig. 2.1). This nucleotide sequence encodes for the Salmonella typhimurium invasion gene D protein (sigD) and invasion gene E protein (sigE) genes. The Sa/monella and the non-Salmonella serovars used were subjected to PCR conditions at various annealing temperatures (T.) (Tables 2.4, 2.5,2.6). This was performed in order to optimize the PCR. Plasmid DNA PCR amplicons (350bp) detected S.braenderup and S.gallinarum at 53oC (Fig. 2.7) and at 56oC, S.braenderup at 54oC and S.gatlinarum at 55oC. PCR of the plasmid DNA did however not detect Salmonella typhimurium, the serotype it was designed to detecen_US
dc.language.isoenen_US
dc.publisherUniversity of the Western Capeen_US
dc.subjectBioformaticsen_US
dc.subjectPolymeraseen_US
dc.subjectchain reactionen_US
dc.subjectSalmonellaen_US
dc.subjecttyphimuriumen_US
dc.subjectspecificityen_US
dc.titleBioinformatics and polymerase chain reaction: Tools to determine the host specificity of Salmonella typhi muriumen_US
dc.rights.holderUniversity of the Western Capeen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record