dc.creatorEspinoza, José
dc.creatorEspinoza, José
dc.date.accessioned2015-06-24T16:45:46Z
dc.date.accessioned2023-05-24T15:14:17Z
dc.date.available2015-06-24T16:45:46Z
dc.date.available2023-05-24T15:14:17Z
dc.date.created2015-06-24T16:45:46Z
dc.date.issued2003-07
dc.identifierEspinoza J. Cloning leishmania telomeres in yeast by complementation. Informe Científico Tecnológico. Volumen 2 (2002) p. 147-149.
dc.identifier1684-1662
dc.identifierhttps://hdl.handle.net/20.500.13054/363
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/6443000
dc.description.abstractLeishmania telemores were cloned in yeast by complementation using a half arm of the yeast artificial chromosome vector pJS97. A single copy marker associated to the telomere (YT2) located 6 kb away from one end of a megabase size chromosome of 1116c8 was cloned by end rescue and DNA sequenced. The sequence of 1479 bp did not show a significant homology with any sequence stored in GenBank. Leishmania telomeres are amenable to be cloned and maintained in yeast, this approach will facilitate the analysis of telomere and subtelomere regions which are usually underrepresented in genomic libraries.
dc.languageeng
dc.publisherLima (Perú)
dc.publisherPE
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceInstituto Peruano de Energía Nuclear
dc.sourceRepositorio Institucional del Instituto Peruano de Energía Nuclear
dc.subjectLeishmania telemores
dc.subjectParásitos
dc.subjectEnfermedad de leishmaniasis
dc.subjectSecuencia de cromosomas
dc.titleCloning leishmania telomeres in yeast by complementation
dc.typeinfo:eu-repo/semantics/article


Este ítem pertenece a la siguiente institución