Incorporation of a bzip transcription factor specific sgRNA into pMZ379 plasmid.
| dc.contributor.advisor | Attila , Papp László | |
| dc.contributor.author | Ken-Ajayi, Emmanoella | |
| dc.contributor.department | DE--Természettudományi és Technológiai Kar--Biológiai és Ökológiai Intézet | |
| dc.date.accessioned | 2025-06-17T12:45:51Z | |
| dc.date.available | 2025-06-17T12:45:51Z | |
| dc.date.created | 2025 | |
| dc.description.abstract | This 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.course | Biochemical Engineering | |
| dc.description.degree | BSc/BA | |
| dc.format.extent | 23 | |
| dc.identifier.uri | https://hdl.handle.net/2437/393062 | |
| dc.language.iso | en | |
| dc.rights.info | Hozzáférhető a 2022 decemberi felsőoktatási törvénymódosítás értelmében. | |
| dc.subject | Plasmids | |
| dc.subject | sgRNA | |
| dc.subject | CRISPR-Cas9 | |
| dc.subject.dspace | Biology::Genetics | |
| dc.title | Incorporation of a bzip transcription factor specific sgRNA into pMZ379 plasmid. |
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