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dc.contributor.advisorŠtěrba, Ján
dc.contributor.authorStemmer, Vitus
dc.date.accessioned2024-03-12T08:12:17Z
dc.date.available2024-03-12T08:12:17Z
dc.date.issued2020
dc.date.submitted2020-08-13
dc.identifier.urihttps://dspace.jcu.cz/handle/20.500.14390/42729
dc.description.abstractA recombinant enzyme PNGase H+ was produced in E. coli, and several steps were tried to optimize the expression, extraction and purification. Furthermore, PCR primers were designed to detect genes of predicted sialyltransferases, fucosyltransferases and DNA methyltransferases in Ixodes ricinus genomic DNA and plasmids were designed for future production of DNA methyltransferases in an insect expression system.cze
dc.format33 p. (53 122 characters)
dc.format33 p. (53 122 characters)
dc.language.isoeng
dc.publisherJihočeská univerzitacze
dc.rightsBez omezení
dc.titleProduction of recombinant proteins using prokaryotic and eukaryotic expression systemscze
dc.title.alternativeProduction of recombinant proteins using prokaryotic and eukaryotic expression systemseng
dc.typebakalářská prácecze
dc.identifier.stag56188
dc.description.abstract-translatedA recombinant enzyme PNGase H+ was produced in E. coli, and several steps were tried to optimize the expression, extraction and purification. Furthermore, PCR primers were designed to detect genes of predicted sialyltransferases, fucosyltransferases and DNA methyltransferases in Ixodes ricinus genomic DNA and plasmids were designed for future production of DNA methyltransferases in an insect expression system.eng
dc.date.accepted2020-09-17
dc.description.departmentPřírodovědecká fakultacze
dc.thesis.degree-disciplineBiological Chemistrycze
dc.thesis.degree-grantorJihočeská univerzita. Přírodovědecká fakultacze
dc.thesis.degree-nameBc.
dc.thesis.degree-programBiochemistrycze
dc.description.gradeDokončená práce s úspěšnou obhajoboucze
dc.contributor.refereeGrinkevich, Pavel


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