R
Richard P. Haugland
Researcher at Molecular Probes
Publications - 175
Citations - 16789
Richard P. Haugland is an academic researcher from Molecular Probes. The author has contributed to research in topics: Fluorescence & Fluorophore. The author has an hindex of 71, co-authored 175 publications receiving 16339 citations. Previous affiliations of Richard P. Haugland include Life Technologies.
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Journal ArticleDOI
A Stable Nonfluorescent Derivative of Resorufin for the Fluorometric Determination of Trace Hydrogen Peroxide: Applications in Detecting the Activity of Phagocyte NADPH Oxidase and Other Oxidases
TL;DR: The enzymatic determination of hydrogen peroxide can be accomplished with high sensitivity and specificity using N-acetyl-3, 7-dihydroxyphenoxazine (Amplex Red), a highly sensitive and chemically stable fluorogenic probe for the enzymatics determination of H2O2.
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Alexa Dyes, a Series of New Fluorescent Dyes that Yield Exceptionally Bright, Photostable Conjugates:
Nataliya Panchuk-Voloshina,Rosaria P. Haugland,Janell Bishop-Stewart,Mahesh K. Bhalgat,Paul J. Millard,Fei Mao,Wai-Yee Leung,Richard P. Haugland +7 more
TL;DR: This work evaluated Alexa dyes compared with conventional dyes in applications using various conjugates, including those of goat anti-mouse IgG (GAM), streptavidin, wheat germ agglutinin (WGA), and concanavalin A (ConA).
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Characterization of PicoGreen Reagent and Development of a Fluorescence-Based Solution Assay for Double-Stranded DNA Quantitation
TL;DR: The PicoGreen assay allowed the detection of 25 pg/ml ds DNA, surpassing the sensitivity achieved with Hoechst 33258 by 400-fold, and showed greater dsDNA:RNA selectivity than HoeChSt 33258 in low ionic strength buffer and better dSDNA:single-stranded DNA selectivity in 1 M NaCl.
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Stable fluorescent complexes of double-stranded DNA with bis-intercalating asymmetric cyanine dyes: properties and applications
Hays S. Rye,Stephen T. Yue,David E. Wemmer,Mark A. Quesada,Richard P. Haugland,Richard A. Mathies,Alexander N. Glazer +6 more
TL;DR: The synthesis, proof of structure, and the absorption and fluorescence properties of two new unsymmetrical cyanine dyes, thiazole orange dimer and oxazole yellow dimer are reported, which form highly fluorescent complexes with double-stranded DNA (dsDNA) with greater than 1000-fold fluorescence enhancement.
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1-[4-(Trimethylamino)phenyl]-6-phenylhexa-1,3,5-triene: synthesis, fluorescence properties, and use as a fluorescence probe of lipid bilayers.
TL;DR: TMA-DPH, a cationic analogue of diphenylhexatriene (DPH), has photophysical properties that are generally similar to those of DPH, and should prove useful in the study of the dynamics of phospholipid monolayers, e.g., in native or reconstituted lipoproteins.