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dc.contributor.authorSung, Ki-Joo
dc.contributor.authorMiller, Eric Alexander
dc.contributor.authorSikes Johnson, Hadley
dc.date.accessioned2018-11-19T19:35:53Z
dc.date.available2018-11-19T19:35:53Z
dc.date.issued2018-10
dc.date.submitted2018-07
dc.identifier.issn2058-9689
dc.identifier.urihttp://hdl.handle.net/1721.1/119208
dc.description.abstractThe hyperthermostable binding scaffold, rcSso7d, has recently been studied for use in in vitro diagnostic tests but has not yet been demonstrated as a soluble reporter protein. Here, we investigated several rcSso7d protein constructs and biotin conjugation methods to link a detectable signal to the presence of a target biomarker.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant 1122374)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistry (RSC)en_US
dc.relation.isversionofhttp://dx.doi.org/ 10.1039/C8ME00049Ben_US
dc.rightsCreative Commons Attribution-NonCommercial 3.0 Unporteden_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/en_US
dc.sourceRoyal Society of Chemistryen_US
dc.titleEngineering Engineering Hyperthermostable rcSso7d as Reporter Molecule for in Vitro Diagnostic Testsen_US
dc.typeArticleen_US
dc.identifier.citationSung, Ki-Joo et al. “Engineering Hyperthermostable rcSso7d as Reporter Molecule for in Vitro Diagnostic Tests.” Molecular Systems Design & Engineering 2018, 5 (October 2018) © 2018 Royal Society of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.mitauthorSung, Ki-Joo
dc.contributor.mitauthorMiller, Eric Alexander
dc.contributor.mitauthorSikes Johnson, Hadley
dc.relation.journalMolecular Systems Design & Engineeringen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsSung, Ki-Joo; Miller, Eric A.; Sikes, Hadley D.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-8120-538X
dc.identifier.orcidhttps://orcid.org/0000-0002-6217-3922
dc.identifier.orcidhttps://orcid.org/0000-0002-7096-138X
mit.licensePUBLISHER_CCen_US


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