Rhodamine red

Potassium perchlorate. Antimony sulfide, Rhodamine red. Dextrin... 

Potassium perchlorate, Antimony sulfide, Rhodamine red, Dextrin Ammonium nitrate, Ammonium perchlorate, Epoxy resin, Aluminum powder... 

Lacquers or varnishes Many metallic cases and components in contact with explosives are protected by coating of lacquers or varnishes. Some varnishes, even after complete curing, have been found to give high gas rates especially with RDX/TNT. Similarly, the compatibility of lacquers is considerably affected by the use of coloring dyes such as rhodamine red dye. 

Zinc dust, hexachloroethane and aluminium Phosphorous pentoxide and phosphoric acid Sulfur, potassium nitrate and pitch Potassium chlorate, naphthalene and charcoal Zinc dust, hexachloroethane and naphthalene Silicon tetrachloride and ammonia vapour Auramine, potassium chlorate, baking soda and sulfur Auramine, lactose, potassium chlorate and chrysoidine Rhodamine red, potassium chlorate, antimony sulfide Rhodamine red, potassium chlorate, baking soda, sulfur Auramine, indigo, potassium chlorate and lactose Malachite green, potassium chlorate, antimony sulfide Indigo, potassium chlorate and lactose Methylene blue, potassium chlorate, antimony sulfide... 

FIGURE 13.5 (a) Visualization of a typical multilamellar ethosome containing 2% PL, 30% ethanol, and water by TEM (b) Entrapment of fluorescent probes by phopholipid vesicles as visualized by CSLM. Liposomes (a-c) or ethosomes (d-f) were prepared with one of three fluorescent probes rhodamine red (a, d), D-289 (b, e), or calceine (c, f). White represents the highest concentration of probe. (Reproduced from Touitou, E. et al., J. Control. Release, 65, 403, 2000. With permission from Elsevier.)... 

Fig. 11.3. Icmt inhibition induces autophagy in HepG2 cells. (A) Autophagy marker, LC3, was analyzed in control and cysmethyrul-treated cells. (B) Detection of autophagosomes. HepG2 cells were treated as in (A) for 48 h and then subjected to immunofluorescence analysis using anti-LC3 and rhodamine-red tagged secondary antibody (red) nuclei were stained with DAPI (blue). This figure is reproduced from Ref. [44].

Figure 4.7 (A) Schematic illustration of fluorescence enhancement experiment Ag nanoprisms are adsorbed on top of monolayer of Rhodamine red on glass slide. (B) Darkfield scattering image of an area of the substrate. Each of colored...

Figure 4.8 Specific DNA-directed coupling of fluorescent dyes to Ag nanoprisms. (A) Darkfield optical micrograph showing a field of isolated Ag nanoprisms. (B) Incubation of the DNA-functionalized particle field in with non-complementary dye-labeled DNA results in little detectable fluorescence. (Q Subsequent hybridization of the same sample with complementary Rhodamine Red-labeled DNA leads to attachment of the dye and visible fluorescence from the functionalized nanoparticles. Reprinted from reference 9.

Figure 4.9 (A) Darkfield optical micrograph of four individual Ag nanoparticles that have been hybridized with a 1 1 mixture of the dyes Alexa Fluor 488 and Rhodamine Red. (B) Fluorescence micrograph of the same area collected using Alexa Fluor 488 excitation eind emission. (C) Fluorescence micrograph of the same area collected using Rhodamine Red excitation and emission. (D) Single particle scattering spectra show the LSPR for each particle in (A). Reprinted from reference 9.

Figure 4.10 Summary of 457 individual particle fluorescence vs. LSPR peak position measurements with three different fluorescent dyes. The LSPR peak positions are binned in 20 nm intervals along the x-axis. The average fluorescence intensity observed from particles within each bin is then plotted as a function of the LSPR position for Ag nanoprisms functionalized with (A) Alexa Fluor 488, (B) Alexa Fluor 532 and (C) Rhodamine Red dyes. The absorption spectra (dotted lines) and emission spectra (dashed lines) are plotted for reference for each dye. The solid...

Fig. 1. Examples of fluorescence preparations of Drosophila whole mounts using the protocols is described in this chapter. All confocal images were obtained with a LeicaTCS4D confocal microscope, (a) Confocal optical section of a D. melanogaster embryo whole mount at blastoderm stage double stained with phalloidin—rhodamine (red) and DAPI (blue) to allow simultaneous visualization of nuclei and cortical actin around cell membranes. Anterior is to the left.

Figure 6.26 (a) CdSe/ZnS QDs for the optical analysis of the protease-mediated hydrolysis of the rhodamine red-X-functionalized peptide 38 (b) Decrease in fluorescence of the dye and corresponding increase in fluorescence of the... 

Rhodamine reds n. A class of clean, blue shade organic reds possessing good lightfastness often called magenta in process printing. 

Organic pigments are used for special purposes. They are generally purer, but more expensive. Examples include Hansa yellow, Irgazin orange and violet, copper phthalocyanine green and blue, toluidine red, para red, Lithol red and rhodamine red (Mathias 1984 Fischer and Adams 1990). 

Fig. 6.1. Absorption and emission spectra of (a) rhodamine red and a genetically encoded protein (DsRed2), (b) six different ZnS-CdSe quantum dot dispersions, (c) A photograph demonstrating the size-tunable fluorescence properties of quantum dot dispersions (reproduced with permission from [887])...

To study whether these HL vectors were affecting transfection activity through pH-sensitive changes in membrane fusion within the endosome to promote escape, Chaudhuri et al. used a fluorescence resonance energy transfer (FRET) technique. HL-l/Chol liposomes were incubated with Rhodamine Red -containing liposomes and subjected to... 

MPDMS nanoparticles are -50.2, -49.4 and —50.6mV, respectively. The zeta potentials of MPMS nanoparticles incorporating fluorescent dye (e.g. rhodamine red) within their interior are not markedly different from those nanoparticles... 

Figure 4.9 Fluorescence microscopy of surface-modified thiol-organosilica and TEOS nanoparticles. Nanoparticles were mixed with rhodamine red-maleimide (upper panels) and with GFP (lower panels) (Reproduced with permission from Ref [50] 2008, American Chemical Society.).

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