Incorporation of a bzip transcription factor specific sgRNA into pMZ379 plasmid.

dc.contributor.advisorAttila , Papp László
dc.contributor.authorKen-Ajayi, Emmanoella
dc.contributor.departmentDE--Természettudományi és Technológiai Kar--Biológiai és Ökológiai Intézet
dc.date.accessioned2025-06-17T12:45:51Z
dc.date.available2025-06-17T12:45:51Z
dc.date.created2025
dc.description.abstractThis thesis outlines the successful incorporation of a Schizosaccharomyces japonicus-specific sgRNA targeting the SJAG_02569 gene into the CRISPR-Cas9 plasmid vector pMZ379. The study highlights the use of CRISPR-Cas9 gene editing to expand molecular tools for S. japonicus, a promising but underutilized model organism. The procedure involved plasmid extraction, PCR amplification using sgRNA-carrying primers, transformation into E. coli DH5α, and verification via colony PCR. Despite technical challenges, including low transformation efficiency and potential template contamination, the study confirmed the correct construction of a recombinant plasmid carrying the desired sgRNA. This newly engineered plasmid will facilitate future genome editing experiments in S. japonicus, addressing the current lack of a CRISPR-Cas9 system for this species.
dc.description.courseBiochemical Engineering
dc.description.degreeBSc/BA
dc.format.extent23
dc.identifier.urihttps://hdl.handle.net/2437/393062
dc.language.isoen
dc.rights.infoHozzáférhető a 2022 decemberi felsőoktatási törvénymódosítás értelmében.
dc.subjectPlasmids
dc.subjectsgRNA
dc.subjectCRISPR-Cas9
dc.subject.dspaceBiology::Genetics
dc.titleIncorporation of a bzip transcription factor specific sgRNA into pMZ379 plasmid.
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