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dc.contributor.authorBukhari, Syed Habib Tahir
dc.contributor.authorAkkineni, Ashwini Rahul
dc.contributor.authorAnanth, Adithya
dc.contributor.authorGordeev, Victor
dc.contributor.authorGrieb, Svea
dc.contributor.authorMansour, Sarah
dc.contributor.authorRoth, Mareike
dc.contributor.authorSampathkumar, Charanya
dc.contributor.authorSchirmer, Lucas
dc.contributor.authorTam, Jonathan
dc.date.accessioned2010-12-05T20:57:12Z
dc.date.available2010-12-05T20:57:12Z
dc.date.issued2010-12-05
dc.identifier.urihttp://hdl.handle.net/1721.1/60087
dc.description.abstractThe Biotec_Dresden Team 2010 developed an approach where two fluorescent proteins are simultaneously expressed. The fact that one reporter, in our case RFP, is constitutively expressed allows to monitor cell growth. Secondly, an inducible promoter drives the expression of the second reporter, YFP in the case of the part tested. The constitutively expressed reporter protein (R1) serves as normalization factor for the inducible reporter (R2) by simple division.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesBBF RFC;78
dc.rightsAttribution-No Derivative Works 3.0 United Statesen
dc.rights.urihttp://creativecommons.org/licenses/by-nd/3.0/us/en
dc.subjectmeasurement standarden_US
dc.titleNovel Normalization Standard using Fluorescenceen_US
dc.typeTechnical Reporten_US


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