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dc.contributor.authorKöse, Semra Özgün
dc.contributor.authorÖziç, Cem
dc.contributor.authorYılmaz, Filiz
dc.contributor.authorErsöz, Arzu
dc.contributor.authorSay, Rıdvan
dc.date.accessioned2019-10-20T14:27:48Z
dc.date.available2019-10-20T14:27:48Z
dc.date.issued2019
dc.identifier.issn1359-5113
dc.identifier.issn1873-3298
dc.identifier.urihttps://dx.doi.org/10.1016/j.procbio.2019.06.011
dc.identifier.urihttps://hdl.handle.net/11421/17833
dc.descriptionWOS: 000481724000023en_US
dc.description.abstractThis study describes the development of cryogel columns prepared by ATP having ruthenium hapten cross-linker based photosensitive approach "ANADOLUCA" for the biotinylation of Crimean Congo Hemorrhagic Fever (CCHF) primers through 5' end as a first. In this process, which does not require ATP ligand, CCHF recognition has been performed using stable and quantum dots (QDs) based avidity nanoparticles cross-linked with streptavidin. p(HEMA-co-DNA ligase) photosensitive copolymerized cryogel column as a biotinylated continuous system have prepared using ATP ligand having photosensitive ruthenium chelate based hapten cross-linker and characterized. Then, the biotinylated efficiency of the prepared column has performed through continuous biotin binding without any need of ATP ligand having to Crimean congo hemorrhagic fever primer (CCHF). The efficiency of the biotinylated CCHF primer has investigated by polymerase chain reaction (PCR). The characteristic of a sustainable biotinylating column synthesized from the same ligand that we normally develop using DNA ligase while working with ATP in the DNA ligase biotinylation process is that it can biotinize without ATP. In addition, virus-identifying ssDNA was observed as fluorescence after avidity interaction with the QD combination for viral identification after biotinylation. Then, the fluorescence intensity changes through the hybridization of 3'-ssDNA complements have determined.en_US
dc.description.sponsorshipBionkit Limited Company; Scientific and Technological Research Council of Turkey (TUBITAK) [1130016]en_US
dc.description.sponsorshipThis study has been partially supported by Bionkit Limited Company and Scientific and Technological Research Council of Turkey (TUBITAK) (Project number 1130016 within the scope of Tubitak 1511 Priority Areas Research Technology Development and Innovation Project Support Program).en_US
dc.language.isoengen_US
dc.publisherElsevier Sci LTDen_US
dc.relation.isversionof10.1016/j.procbio.2019.06.011en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCrimean Congo Hemorrhagic Fever (Cchf)en_US
dc.subjectDna Ligaseen_US
dc.subjectCryogel Columnsen_US
dc.subjectQuantum Dots (Qds)en_US
dc.subjectBiotinylationen_US
dc.subjectUnneeded Atp Biotinylation Processen_US
dc.titleDNA ligase photocrosslinked cryogenic column based biotinylation kit for viral hybridization and detectionen_US
dc.typearticleen_US
dc.relation.journalProcess Biochemistryen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Kimya Bölümüen_US
dc.identifier.volume84en_US
dc.identifier.startpage213en_US
dc.identifier.endpage219en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US]
dc.contributor.institutionauthorYılmaz, Filiz
dc.contributor.institutionauthorErsöz, Arzu
dc.contributor.institutionauthorSay, Rıdvan


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