dc.creatorDebue M.
dc.creatorGautier P.
dc.creatorHackel C.
dc.creatorVan Elsen A.
dc.creatorHerzog A.
dc.creatorBigaignon G.
dc.creatorBollen A.
dc.date1991
dc.date2015-06-30T14:09:42Z
dc.date2015-11-26T14:42:04Z
dc.date2015-06-30T14:09:42Z
dc.date2015-11-26T14:42:04Z
dc.date.accessioned2018-03-28T21:49:25Z
dc.date.available2018-03-28T21:49:25Z
dc.identifier
dc.identifierResearch In Microbiology. , v. 142, n. 5, p. 565 - 572, 1991.
dc.identifier9232508
dc.identifier10.1016/0923-2508(91)90189-H
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0025887087&partnerID=40&md5=f9143e948859988b0f6349895410e0eb
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/99225
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/99225
dc.identifier2-s2.0-0025887087
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1251115
dc.descriptionOligonucleotide primers were used in the polymerase chain reaction assay to amplify specific DNA regions of the Borrelia burgdorferi 49-kb linear plasmid. One set of primers identifies a 442-bp DNA fragment in the OspA gene and a second pair of amplimers, a 176-bp DNA piece located in the OspB gene. The last set of primers. OspBpc3/pc4. outperformed the other pair in discriminating pathogenic North American or European isolates from related bacterial species, detected down to 4 spirochaetes, and was suitable for the identification of B. burgdorferi in biological samples, such as synovial and cerebrospinal fluids. © 1991.
dc.description142
dc.description5
dc.description565
dc.description572
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dc.languageen
dc.publisher
dc.relationResearch in Microbiology
dc.rightsfechado
dc.sourceScopus
dc.titleDetection Of Borrelia Burgdorferi In Biological Samples Using The Polymerase Chain Reaction Assay
dc.typeArtículos de revistas


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