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Journal of Biomolecular Screening|September 24, 2011
A substrate-independent TR-FRET histone deacetylase inhibitor assayBryan D Marks, Stephen A Fakhoury, William J Frazee, et al.Assay and Drug Development Technologies|January 28, 2006
Multiparameter analysis of a screen for progesterone receptor ligands: comparing fluorescence lifetime and fluorescence polarization measurementsBryan D Marks, Naveeda Qadir, Hildegard C Eliason, et al.Assay and Drug Development Technologies|May 29, 2004
Overcoming compound interference in fluorescence polarization-based kinase assays using far-red tracersKevin L Vedvik, Hildegard C Eliason, Randy L Hoffman, et al.Journal of Biomolecular Screening|July 1, 2009
Development and applications of a broad-coverage, TR-FRET-based kinase binding assay platformConnie S Lebakken, Steven M Riddle, Upinder Singh, et al.Biochemistry|January 17, 2007
The androgen receptor T877A mutant recruits LXXLL and FXXLF peptides differently than wild-type androgen receptor in a time-resolved fluorescence resonance energy transfer assayMary Szatkowski Ozers, Bryan D Marks, Krishne Gowda, et al.Assay and Drug Development Technologies|June 10, 2009
Identification of pregnane X receptor ligands using time-resolved fluorescence resonance energy transfer and quantitative high-throughput screeningSunita J Shukla, Dac-Trung Nguyen, Ryan Macarthur, et al.Assay and Drug Development Technologies|May 13, 2008
Development of the predictor HERG fluorescence polarization assay using a membrane protein enrichment approachDavid R Piper, Steve R Duff, Hildegard C Eliason, et al.Pageof 1