Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/11700
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dc.contributor.authorJurisic, Vladimir-
dc.contributor.authorObradović, Jasmina-
dc.contributor.authorTosic, Natasa-
dc.contributor.authorPavlović, Sonja-
dc.contributor.authorKulic Milan-
dc.contributor.authorDjordjevic, Natasa-
dc.date.accessioned2021-04-20T19:00:55Z-
dc.date.available2021-04-20T19:00:55Z-
dc.date.issued2016-
dc.identifier.issn0731-7085-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/11700-
dc.description.abstract© 2016. The aim of the study was to examine the effects of frequently used polymerase chain reaction (PCR) additives DMSO, glycerol and betaine on amplification of GC-rich epidermal growth factor receptor (EGFR) gene promoter region, in order to detect the presence of -216G > T and -191C > A gene variations in non-small-cell lung cancer (NSCLC) patients. PCR products and restriction fragments were detected by electrophoresis on 8% polyacrylamide gel and 3% agarose gel. Our analysis shows that single used additives including DMSO in concentration of 7% and 10%, glycerol in concentration of 10%, 15% and 20%, as well as betaine in concentration of 1 M, 1.5 M and 2 M significantly enhanced the yield and specificity of PCR reaction. In addition, the combination of 10% DMSO with 15% glycerol has shown positive effects, whereas other analyzed combinations of additives failed to amplify the EGFR promoter region.-
dc.rightsrestrictedAccess-
dc.sourceJournal of Pharmaceutical and Biomedical Analysis-
dc.titleEffects of DMSO, glycerol, betaine and their combinations in detecting single nucleotide polymorphisms of epidermal growth factor receptor (EGFR) gene promoter sequence in non-small-cell lung cancer (NSCLC) patients-
dc.typearticle-
dc.identifier.doi10.1016/j.jpba.2016.05.010-
dc.identifier.scopus2-s2.0-84973129537-
Appears in Collections:Faculty of Medical Sciences, Kragujevac
Institute for Information Technologies, Kragujevac

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