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dc.contributor.authorOrtega Rivas, Antonio 
dc.contributor.authorMartínez Carretero, Enrique 
dc.contributor.authorAlonso, V.
dc.contributor.authorQuispe, A.
dc.contributor.authorThomas, M.C .
dc.contributor.authorAlonso, R.
dc.contributor.authorPiñero Barroso, José Enrique 
dc.contributor.authorGonzález, A.C.
dc.contributor.authorValladares Hernández, Basilio 
dc.contributor.otherDidácticas Específicas
dc.contributor.otherInstituto de Enfermedades Tropicales y Salud Pública de Canarias
dc.date.accessioned2024-09-23T20:05:13Z
dc.date.available2024-09-23T20:05:13Z
dc.date.issued2003
dc.identifier.urihttp://riull.ull.es/xmlui/handle/915/38839
dc.description.abstractThe technique of Random Amplification Polymorphic DNA allows fragments of the genome to be amplified by means of polymerase chain reaction (PCR) without previous knowledge of their sequences. The protozoa of the genus Leishmania present great genetic variability, making it difficult to characterize the different species. A method is developed with a single 10-mers long primer, which allows the species L. braziliensis, L. mexicana, L. infantum, L. tropica, L. chagasi, L. amazonensis and L. major to be differentiated. These products amplified by RAPD have also facilitated the design of some primers that amplify L. braziliensis DNA exclusively.en
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.relation.ispartofseriesParasitology (2003), 127
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.titleRAPD method useful for distinguishing Leishmania species: design of specific primers for L. braziliensis.en
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1017/S0031182003004104
dc.subject.keywordRAPD
dc.subject.keywordPCR
dc.subject.keywordprimer
dc.subject.keywordLeishmania braziliensis


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