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dc.contributor.advisorDvořák, Jan
dc.contributor.authorOpavský, David
dc.date.accessioned2021-12-06T14:05:22Z
dc.date.available2021-12-06T14:05:22Z
dc.date.issued2013
dc.date.submitted2013-04-26
dc.identifier.urihttps://dspace.jcu.cz/handle/20.500.14390/24433
dc.description.abstractSmSP1 is a chimerical serine protease consisted of three domains (cub, LDLa and trypsin-like) and found in Schistosoma mansoni. Its characterization was performed by molecular techniques such as PCR screen, qRT-PCR and RNA interference (RNAi) to gain information about expression profile, level expression and susceptibility to RNAi. Further, protein expression was carried out to gain an antigen for immunization and recombinant for biochemical studies. Results of PCR screen and qRT-PCR suggested possible function of SmSP1 in egg and adult stages but SmSP1 gene was not found susceptible to RNAi in NTS. Recombinant from E. coli was successfully used for immunization. Active recombinant was likely expressed in Pichia pastoris but expression conditions are unstable and expression optimization is necessary.cze
dc.format62 s.
dc.format62 s.
dc.language.isoeng
dc.publisherJihočeská univerzitacze
dc.rightsBez omezení
dc.subjectSchistosoma mansonicze
dc.subjectserine proteasecze
dc.subjectPCR screencze
dc.subjectqRT-PCRcze
dc.subjectRNA interferencecze
dc.subjectantigencze
dc.subjectimmunizationcze
dc.subjectSchistosoma mansonieng
dc.subjectserine proteaseeng
dc.subjectPCR screeneng
dc.subjectqRT-PCReng
dc.subjectRNA interferenceeng
dc.subjectantigeneng
dc.subjectimmunizationeng
dc.titleMolecular and biochemical characterization of serine protease SmSP1 in <i>Schistosoma mansoni</i>cze
dc.title.alternativeMolecular and biochemical characterization of serine protease SmSP1 in <i>Schistosoma mansoni</i>eng
dc.typediplomová prácecze
dc.identifier.stag18616
dc.description.abstract-translatedSmSP1 is a chimerical serine protease consisted of three domains (cub, LDLa and trypsin-like) and found in Schistosoma mansoni. Its characterization was performed by molecular techniques such as PCR screen, qRT-PCR and RNA interference (RNAi) to gain information about expression profile, level expression and susceptibility to RNAi. Further, protein expression was carried out to gain an antigen for immunization and recombinant for biochemical studies. Results of PCR screen and qRT-PCR suggested possible function of SmSP1 in egg and adult stages but SmSP1 gene was not found susceptible to RNAi in NTS. Recombinant from E. coli was successfully used for immunization. Active recombinant was likely expressed in Pichia pastoris but expression conditions are unstable and expression optimization is necessary.eng
dc.date.accepted2013-05-27
dc.description.departmentPřírodovědecká fakultacze
dc.thesis.degree-disciplineExperimentální biologie - specializace Buněčná a vývojová biologiecze
dc.thesis.degree-grantorJihočeská univerzita. Přírodovědecká fakultacze
dc.thesis.degree-nameMgr.
dc.thesis.degree-programBiologiecze
dc.description.gradeDokončená práce s úspěšnou obhajoboucze
dc.contributor.refereeKašný, Martin
dc.contributor.refereeSojka, Daniel


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