Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7171
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dc.contributor.authorBeal, Jacoben_US
dc.contributor.authoriGEM Interlab Study Contributorsen_US
dc.contributor.authorATHALE, CHAITANYA A. et al.en_US
dc.date.accessioned2022-06-24T10:42:12Z-
dc.date.available2022-06-24T10:42:12Z-
dc.date.issued2016-03en_US
dc.identifier.citationPLOS One,11(3).en_US
dc.identifier.issn1932-6203en_US
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0150182en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7171-
dc.description.abstractWe present results of the first large-scale interlaboratory study carried out in synthetic biology, as part of the 2014 and 2015 International Genetically Engineered Machine (iGEM) competitions. Participants at 88 institutions around the world measured fluorescence from three engineered constitutive constructs in E. coli. Few participants were able to measure absolute fluorescence, so data was analyzed in terms of ratios. Precision was strongly related to fluorescent strength, ranging from 1.54-fold standard deviation for the ratio between strong promoters to 5.75-fold for the ratio between the strongest and weakest promoter, and while host strain did not affect expression ratios, choice of instrument did. This result shows that high quantitative precision and reproducibility of results is possible, while at the same time indicating areas needing improved laboratory practices.en_US
dc.language.isoenen_US
dc.publisherPLOSen_US
dc.subjectCalibrationen_US
dc.subjectStandarden_US
dc.subject2016en_US
dc.titleReproducibility of Fluorescent Expression from Engineered Biological Constructs in E-colien_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitlePLOS Oneen_US
dc.publication.originofpublisherForeignen_US
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