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DyesTRITCAntibodyWavelengthFluorescence emissionSpectraFITCPhalloidinDegradationFluorescent dyeWavelengthsAlexa FluorLissamine525nmFluoresceinDerivativesLuminescenceMulticolor emissionScanning electron mSingle moleculeFluorophore2016DiffractionTetramethylrhodamineEsterColorsPeakMolecularDAPISynthesisCoordinatesExhibitsIntensityCharacteristicRatioProbePowderOrganicFilterImageFilmVisible
Dyes8
  • Rhodamine dyes fluoresce and can thus be detected easily and inexpensively with instruments called fluorometers. (wikipedia.org)
  • Rhodamine dyes are used extensively in biotechnology applications such as fluorescence microscopy, flow cytometry, fluorescence correlation spectroscopy and ELISA. (wikipedia.org)
  • R. F. Kubin and A. N. Fletcher, "Fluorescence quantum yields of some rhodamine dyes. (wikipedia.org)
  • ROX dyes have longer excitation and emission wavelengths than the other 'conventional' rhodamines. (anaspec.com)
  • DyLight fluorescent dyes are direct alternatives to traditional fluorophores such as fluorescein (FITC) and rhodamine. (vectorlabs.com)
  • The longer excitations and emissions of Rhod-2 make the indicator useful for experiments in cells and tissues that have high levels of autofluorescence and for multiplexing with other fluorescent dyes of shorter wavelengths. (abcam.com)
  • The emission bandpass region is somewhat lower in wavelength than that of the B-1E and B-2E filter sets to provide optimum detection of popular fluorochromes such as FITC, BODIPY, Fluo-3, oxacarbocyanine dyes ( DiO ), and green fluorescent protein ( GFP ). (microscopyu.com)
  • Masked rhodamine dyes of five principal colors revealed by photolysis of a 2-diazo-1-indanone caging group: synthesis, photophysics, and light microscopy applications. (mpg.de)
TRITC1
  • Rhodamine phalloidin is a high-affinity F-actin probe conjugated to the red-orange fluorescent dye, tetramethylrhodamine (TRITC). (thermofisher.com)
Antibody1
  • Rhodamine conjugated anti actin hFAB antibody, clone AbD22606 (12004163) used as a loading control for western blottinng analysis ofcadherin protein expression in cell lysates. (bio-rad-antibodies.com)
Wavelength2
  • It offers improved cell loading and Ca 2 + response while maintaining the convenient Fluo-3 and Fluo-4 spectral wavelength of maximum excitation at 490 nm and maximum emission at 520 nm. (abcam.com)
  • The bandpass emission filter has a center wavelength of 535 nanometers (40-nanometer bandpass), and in similarity to the other filter combinations in this group, the B-2E/C set employs a longpass dichromatic mirror with a cut-on wavelength of 505 nanometers. (microscopyu.com)
Fluorescence emission2
  • It has peak fluorescence emission at 572-575 nm. (creativepegworks.com)
  • Presented in Figure 2(a) is the fluorescence emission intensity from a culture of rat kangaroo ( PtK2 ) epithelial cells that were immunofluorescently labeled with primary anti-bovine alpha -tubulin mouse monoclonal antibodies followed by goat anti-mouse Fab fragments conjugated to Alexa Fluor 488. (microscopyu.com)
Spectra5
  • Figure 3 (center) shows a volumetric display composed of both red and blue-green voxels, which was generated using a fluorescent screen with three layers: two containing coumarin 481 and one containing rhodamine B. Figure 3 (left) and (right) show the fluorescence spectra of coumarin 481 and rhodamine B, respectively. (spie.org)
  • Left: Fluorescence excitation and emission spectra of coumarin 481. (spie.org)
  • Center: Volumetric display with fluorescent layers of different colors obtained by using coumarin 481 and rhodamine B. Right: Fluorescence excitation and emission spectra of rhodamine B. (spie.org)
  • The excitation and emission spectra parallel that of other commercially available fluorescent reagents allowing for easy substitution into an existing protocol without requiring any further instrumentation or filter sets. (vectorlabs.com)
  • Spectroscopic characterization exhibit wide excitation spectrum according to chelating structure of used complexes and characteristic Tb3+ and Eu3+ emission peaks in luminescence spectra. (photonics.pl)
FITC1
  • FITC /GFP: 470/40 nm excitation, 525/50 nm emission. (bidmc.org)
Phalloidin4
  • Demonstrating very little nonspecific staining, Rhodamine phalloidin allows high-contrast discrimination of actin staining. (thermofisher.com)
  • Rhodamine phalloidin is one of the most commonly used fluorescent phalloidin conjugates in the literature, as evidenced by over 1,500 citations (maintained in our in-house database). (thermofisher.com)
  • Rhodamine phalloidin can be used to visualize and quantitate F-actin in tissue sections, cell cultures, or cell-free preparations. (thermofisher.com)
  • Rhodamine phalloidin staining is fully compatible with other fluorescent stains used in cellular analyses including fluorescent proteins, Qdot nanocrystals, and Alexa Fluor conjugates including secondary antibodies. (thermofisher.com)
Degradation6
  • Finally, photocatalytic activity of the samples towards degradation of rhodamine B dye was checked under visible light irradiation. (scirp.org)
  • Further, these nanocomposites were used for the photocatalytic degradation of rhodamine B under solar light irradiation. (ias.ac.in)
  • This work is focused on the study of photoelectrocatalytic degradation of Rhodamine B (RhB) dye by RuO 2 /IrO 2 /TaO 2 coated titanium electrodes. (e-ijep.co.in)
  • The GC-MS confirms the degradation of Rhodamine B from aqueous solution. (e-ijep.co.in)
  • 2014. Visible light photoele-ctrocatalytic degradation of Rhodamine B using a dye-sensitised TiO2electrode. (e-ijep.co.in)
  • 2009. Visible light-driven photocatalytic degradation of Rhodamine B over NaBiO3pathways and mechanisms. (e-ijep.co.in)
Fluorescent dye2
  • Rhodamine is a common red fluorescent dye tracer in biology for staining cells, tissues, biomarkers or nanoparticles. (creativepegworks.com)
  • The samples were filled with gutta-percha using AH Plus sealer with rhodamine B fluorescent dye. (bvsalud.org)
Wavelengths2
  • In addition, the lowered emission filter bandpass results in improved blocking of yellow to red wavelengths, with only green fluorescence appearing in images acquired using the B-2E/C filter combination (See Figure 2). (microscopyu.com)
  • The Label IT Nucleic Acid Labeling Reagents covalently attach CX-rhodamine, fluorescein, digoxin, biotin, Cy™3, Cy™5, dinitrophenol (DNP), and TM-rhodamine labels to nucleic acid bases within DNA or RNA without impacting hybridization performance, and therefore can be used in almost any molecular biology application (excitation and emission wavelengths for each fluorescent Label IT Reagent are listed in Table 1). (pdfmedarticles.com)
Alexa Fluor3
  • Rhodamine Red-X is particularly useful for 3- and 4-color labeling with DyLight 405, Alexa Fluor® 488, and Alexa Fluor® 647 by using a confocal microscope equipped with a 405 nm laser and a krypton/argon laser. (jacksonimmuno.com)
  • The absorption maximum of Alexa Fluor 488 is 495 nanometers and the emission maximum occurs at 519 nanometers. (microscopyu.com)
  • The specimen was simultaneously labeled with primary anti-human OxPhos Complex V inhibitor protein mouse monoclonal antibodies followed by goat anti-mouse Fab fragments conjugated to Alexa Fluor 555 (emission maximum at 571 nanometers). (microscopyu.com)
Lissamine1
  • A commonly used fluorophore pair for RET is N(7-nitrobenz-2-oxa-1,3-diazol-4-yl) phosphatidylethanolamine (N-NBD-PE) and N-(lissamine rhodamine B sulfonyl) PE (N-Rh-PE). (encapsula.com)
525nm1
  • Cellular analyse / detektionssystem: excitation af fluorophoren som Rhodamin, Cy®3, resorufin at 525nm, emission bølgelængde 580-640nm. (strato.de)
Fluorescein1
  • Label IT® CX-Rhodamine Labeling Kit Label IT® Fluorescein Labeling Kit Label IT® TM-Rhodamine Labeling Kit *Each Full Size Kit contains sufficient reagents to Label 100 µg of nucleic acid. (pdfmedarticles.com)
Derivatives1
Luminescence1
  • Among them, it is possible to identify excited-state intramolecular proton transfer, 2 aggregate formation, and conformational change to induce simultaneous locally excited and charge-transfer luminescence 3 including the combination of monomer and excimer emission, 4 stimulation of dual fluorescence and phosphorescence. (rsc.org)
Multicolor emission2
  • The implementation of multicolor emission from a single molecule or a single component material remains a substantial challenge for molecular design and engineering. (rsc.org)
  • The article presents multicolor emission observed in poly(methyl methacrylate) specimens co-doped by trivalent terbium and europium ions. (photonics.pl)
Scanning electron m2
  • Field emission scanning electron microscopy revealed the existence of pyramidal shaped iron oxide in AFC. (scirp.org)
  • The as-prepared CT nanocomposites were characterizedby powder X-ray diffraction, field emission scanning electron microscopy, Raman spectroscopy, transmission electron microscopy and X-ray photoelectron spectroscopy to evaluate their structures and properties. (ias.ac.in)
Single molecule2
  • The construction of tunable multicolor photoluminescent compounds and single molecule-based materials, particularly those capable of efficient white-light emission, continues to be an appealing research topic. (rsc.org)
  • Rhodamine spiroamides for multicolor single-molecule switching fluorescent nanoscopy. (mpg.de)
Fluorophore1
  • This phenomenon is caused by the overlapping of the emission energy band of the donor fluorophore with the excitation energy band of the acceptor fluorophore. (encapsula.com)
20162
  • P. Miluski, M. Kochanowicz, J. Żmojda, and D. Dorosz, "Emission properties and energy transfer in Perylene-Rhodamine 6 G co-doped polymeric fiber", Chinese Optics Letters 14, 12, 121602 (2016). (photonics.pl)
  • 2016. Decolourization of Rhodamine B from aqueous by electrochemical oxidation using graphite electrodes. (e-ijep.co.in)
Diffraction1
  • The structural property of samples was characterized by X-ray diffraction and field emission scanning electron microscope whereas the spectral properties were measured by using UV-Vis, FTIR and Raman spectral studies. (scirp.org)
Tetramethylrhodamine1
  • mPEG-Rhodamine is a linear monofunctional PEG reagent with a tetramethylrhodamine. (creativepegworks.com)
Ester1
  • The AM ester forms of these rhodamine-based indicators are cationic, which can result in potential-driven uptake into mitochondria. (abcam.com)
Colors2
  • 1 For example, in order to achieve white light emission, a chromophore molecule should generate two complementing bands ( e.g. blue and orange) or produce a combination of pure red, green and blue colors. (rsc.org)
  • 9a,c,e Pure colors and very sharp emission bands, long lifetimes and large Stokes shifts of Ln( III ) f → f transitions are beneficial characteristics for responsive molecular materials, i.e. chemosensors, 10b,11 molecular thermometers, 12 biological probes and imaging agents. (rsc.org)
Peak3
  • RRX (Rhodamine Red-X) conjugates have a peak of excitation at 570 nm and a peak of emission at 590 nm. (jacksonimmuno.com)
  • Rhodamine 123 is a fluorescent compound with an excitation peak at 508 nm and an emission peak at 528 nm. (aatbio.com)
  • Note: if an excitation source is added to the graph, the rightmost column in the information table at the bottom of the page, (labeled 'Peak Intensity' with the excitation source title in parentheses) will show the percentage of the maximum possible intensity for the emission curve of each compound currently on the graph. (aatbio.com)
Molecular3
  • Recent progress achieved for panchromatic pure organic and metal-organic luminophores illustrates that multi-band single-molecular emission can be realized via different physical phenomena. (rsc.org)
  • Rhodamine Red-X is a trademark of Molecular Probes, Inc. Jackson ImmunoResearch is licensed by Molecular Probes, Inc. to manufacture and sell conjugates of Rhodamine Red-X reactive dye. (jacksonimmuno.com)
  • J.-H. Jou, M.-C. Sun, H.-H. Chou, C.-H. Li, "White organic light-emitting devices with a solution-processed and molecular host-employed emission layer", Appl. (photonics.pl)
DAPI1
  • DAPI: 365 nm excitation, 445/50 nm emission. (bidmc.org)
Synthesis1
Coordinates1
  • The calculated CIE 1931 chromaticity coordinates confirm that colorful emission from green to red can be obtained using proposed materials. (photonics.pl)
Exhibits2
  • It exhibits excitation ratiometry at 340 nm/380 nm with emission at 505 nm. (abcam.com)
  • Rather than being excitation ratiometric, it exhibits an emission ratio at 475 nm/405 nm when excited at 346 nm. (abcam.com)
Intensity1
  • The displayed graphs show the normalized intensity of each compound, with the excitation curve being represented by a hollow dotted line, and the emission curve being a solid line, filled in with the color of the instrument laser used. (aatbio.com)
Characteristic1
  • Due to the charge transfer characteristic of the excited state, Au1-Au3 reveal significant emission solvatochromism (particularly discernible for Au2 , 428 nm in cyclohexane → 580 nm in acetonitrile). (rsc.org)
Ratio2
  • The Nikon B-2E/C fluorescence filter set is designed as a high-performance combination with a medium-width excitation bandpass (30 nanometers) in order to provide a high signal-to-noise ratio in conjunction with a slightly lowered emission bandpass region compared to the B-1E and B-2E sets. (microscopyu.com)
  • Among the Nikon blue-excitation filter sets, those in the E -series, in general, produce images with a much higher signal-to-noise ratio and darker background regions than do combinations with longpass emission filters. (microscopyu.com)
Probe1
  • Nuclei were stained with the far-red fluorescent probe TO-PRO-3 (emission maximum at 661 nanometers). (microscopyu.com)
Powder1
  • Rhodamine 6G chloride is a bronze/red powder with the chemical formula C28H31ClN2O3. (wikipedia.org)
Organic2
  • One possibility is the use of organic light-emitting molecules such as rhodamine B. The researchers embedded molecules of rhodamine B in a polymer matrix that was then poured onto the surface of a silver film. (phys.org)
  • R. Mac Ciarnain, D. Michaelis, T. Wehlus, A. F. Rausch, N. Danz, A. Brauer, A. Tünnermann, "Emission from outside of the emission layer in state-of-the-art phosphorescent organic light-emitting diodes", Organic Electronics 44, 115 (2017). (photonics.pl)
Filter1
  • By adding a 405 nm laser and a 420 nm emission filter, 4-color labeling is possible using DyLight 405-conjugated secondary antibodies from JIR (Figure 5). (jacksonimmuno.com)
Image1
  • It is then possible to develop an image of the fingerprint by autoradiography, treated fingerprint is placed in contact with a film sensitive to radioactive emissions. (australianpolice.com.au)
Film2
  • Surface plasmon-coupled emission on metallic film coated with dye-doped polymer nanogratings. (phys.org)
  • 2004. Ultraviolet emission of ZnO film prepared by electrophoretic deposition. (e-ijep.co.in)
Visible1
  • 2013. Dye-sensitization-induced visible-light reduction of graphene oxide for the en-hanced TiO2photocatalytic performance. (e-ijep.co.in)