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dc.contributor.authorMohos, Szilvia
dc.date.accessioned2014-01-07T08:29:48Z
dc.date.available2014-01-07T08:29:48Z
dc.date.issued2013
dc.identifier.urihttp://hdl.handle.net/10832/901
dc.description.abstractThe aim of my work was the experimental examination of the disordered regions to verify my hypothesis. For this it was necessary to produce the wild-type Nudix DR0550 protein. I cloned the DNA region coding for the enzyme, cloned it into an expression vector, purified the protein and measured the enzyme activity. I worked with the wild-type as well as with the Nudix-dN mutant which is truncated at its N-terminal, lacking the longer disordered region.en
dc.language.isohuen
dc.subjectBaktériumoken
dc.subjectDNSen
dc.subjectKlónozásen
dc.subjectBacteriaen
dc.subjectDNAen
dc.subjectcloningen
dc.titleA Deinococcus radiodurans Nudix fehérjéjének klónozása, expressziója és enzimaktivitásának méréseen
dc.typeThesisen


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