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dc.contributor.authorWani, M.A.vi
dc.contributor.otherGanaie, A.A.vi
dc.date.accessioned2021-04-20T09:49:34Z-
dc.date.available2021-04-20T09:49:34Z-
dc.date.issued2019-
dc.identifier.issn2522-8307vi
dc.identifier.urihttp://tailieuso.tlu.edu.vn/handle/DHTL/10751-
dc.description.abstractFrom TrxG, ISWI and Acf were selected, and from PcG, Pc and Psc were selected. Three pAc-sgRNA-Cas9-puro-vector constructs for ISWI gene, one pAc-sgRNA-cas9-puro-vector construct for Pc, gene and two pAc-sgRNA-cas9-puro-vector constructs for each of the Acf and Psc gene were generated. These constructs were confirmed by PCR and sequencing. In the future, these constructs will be used to study the role of their respective target genes in chromatin organization.vi
dc.description.urihttps://bnrc.springeropen.com/articles/10.1186/s42269-019-0141-7#article-infovi
dc.languageenvi
dc.relation.ispartofseriesBulletin of the National Research Centre, Vol 43:104 (2019)vi
dc.subjectTrithorax group proteinsvi
dc.subjectPolycomb group proteinsvi
dc.subjectCRISPR-cas9vi
dc.titleGeneration of CRISPR-cas9 construct for knockout of genes encoding chromatin-associated proteinsvi
dc.typeBBvi
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