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dc.contributor.authorAğel, Esra
dc.contributor.authorSağcan, Hasan
dc.date.accessioned2020-11-12T10:04:28Z
dc.date.available2020-11-12T10:04:28Z
dc.date.issued2020en_US
dc.identifier.citationAğel, E. ve Sağcan, H. (2020). Optimization of lyophilized LAMP and RT-PCR reaction mixes for detection of tuberculosis. The EuroBiotech Journal, 4(4), 230-236. https://dx.doi.org/10.2478/ebtj-2020-0027en_US
dc.identifier.issn2564-615X
dc.identifier.urihttps://dx.doi.org/10.2478/ebtj-2020-0027
dc.identifier.urihttps://hdl.handle.net/20.500.12511/6020
dc.description.abstractUndoubtedly, one of the most infectious diseases in the world is tuberculosis. Key factor for tuberculosis control is to prevent possible contagion with rapid diagnosis and effective treatment. The culture method, which it takes several weeks to obtain results, is the gold standard method for laboratory diagnosis of tuberculosis. In order to prevent possible contagion of tuberculosis, diagnosis must be made in short time and treatment should be started as soon as possible. Normally, clinical samples are studied in advanced laboratories designed for this purpose. However, especially after the screening in rural areas, the transmission of the samples to the centers has many negative effects on the clinical material. Therefore, the latest trend molecular techniques in microbiological diagnosis are developing into point of care systems that can be applied in the field without laboratory infrastructure. The major challenge for molecular-based point-of-care tests is the need to store polymerase enzymes and some of the ingredients used in the cold chain. The aim of this study is to increase the resistance of the amplification reaction mixtures by lyophilizing the tuberculosis diagnosis. Lyophilization was performed on Loop-mediated isothermal amplification (LAMP) and Real-time PCR mixtures. For the lyophilization of LAMP and RT-PCR mixtures, two different experimental setups were tried from the literature except for the developed content. Chemicals such as stachyose, trehalose, glycerol and PEG 8000 are widely using as cryoprotectants. As a result, the developed content (0.5% PEG 8000, 2.0 % Stachyose) was determined the best cryoprotectant mixture. Accordingly, amplification mixtures can be produced with the developed lyophilization method and point of care kits can be developed.en_US
dc.language.isoengen_US
dc.publisherSciendoen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectLyophilized Master Mixen_US
dc.subjectLoop-Mediated Isothermal Amplificationen_US
dc.subjectLAMPen_US
dc.subjectReal-Time PCRen_US
dc.subjectM. Tuberculosisen_US
dc.titleOptimization of lyophilized LAMP and RT-PCR reaction mixes for detection of tuberculosisen_US
dc.typearticleen_US
dc.relation.ispartofThe EuroBiotech Journalen_US
dc.departmentİstanbul Medipol Üniversitesi, Sağlık Hizmetleri Meslek Yüksekokulu, Tıbbi Laboratuvar Teknikleri Ana Bilim Dalıen_US
dc.identifier.volume4en_US
dc.identifier.issue4en_US
dc.identifier.startpage230en_US
dc.identifier.endpage236en_US
dc.relation.ecinfo:eu-repo/grantAgreement/TUBITAK/SOBAG/1003 115R002
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.2478/ebtj-2020-0027en_US


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