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Rhodamine 110 chloride

Manufactured by Merck Group
Sourced in United States

Rhodamine 110 chloride is a fluorescent dye commonly used in laboratory applications. It has an excitation wavelength of approximately 496 nm and an emission wavelength of around 520 nm, making it suitable for various fluorescence-based techniques. The dye is often used as a labeling agent or a component in assays and experiments that require fluorescent detection or visualization.

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4 protocols using rhodamine 110 chloride

1

Rhodamine and MTT Assay Protocol

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Rhodamine B chloride, rhodamine 110 chloride, rhodamine 123, phosphate buffered saline (10× concentrate, 0.2 µM filtered), sodium tetraphenylborate [Na][TPB], dichloromethane (DCM), dimethylsulfoxide (DMSO), 1-octanol, sodium hydroxide (NaOH), citric acid monohydrate, and sodium phosphate dibasic were all purchased from Sigma-Aldrich (Milwaukee, WI, USA). Lithium bis(perfluoroethylsulfonyl)imide ([Li][BETI]) was obtained from Ionic Liquid Technologies (Tuscaloosa, Al, USA). Triply deionized water was obtained using an Aires High Purity Water System (Port Allen, LA, USA). The MTT (3-[4,5-Dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) cell viability assay was purchased from Promega Corporation (Madison, WI, USA). TEM grids were purchased from Ted Pella (Redding, CA, USA). SNAFR-5 dye was provided to us by one of our coauthors, Dr. Robert Strongin (Portland State University, Portland, OR, USA).
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2

Characterization of Colloidal Dispersions

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C11(C=O)EO15–CH3, MPD (Nikko Chemicals, assay 99%),
C12EO15, PDE (Nikko Chemicals, assay +99%),
dodecyl dimethyl amine oxide (DDAO, Sigma-Aldrich, 30% aqueous solution),
sodium dodecyl sulfate (SDS, Sigma-Aldrich, assay 99%), propylene
carbonate (PC, Sigma-Aldrich, assay 99%), 2-butanone (MEK, Sigma-Aldrich,
purity 99%), 2-butanol (BuOH, Sigma-Aldrich, assay >99%), ethyl
acetate
(EtAc, Sigma-Aldrich, ACS Reagents, assay ≥99.5%), and the
fluorescent probes used for CLSM experiments, i.e., rhodamine 110
chloride, Nile red, coumarin 6 (Sigma-Aldrich, purity >98−99%),
and Bodipy 558/568 C12 (4,4-difluoro-5-(2- thienyl)-4-bora-3a,4a-diaza-s-indacene-3-dodecanoic acid) (Thermo Fisher) were used
without further purification. Water was purified with a Millipore
Milli-Q gradient system (resistivity >18 MΩ cm). Carbon black,
iron oxide (ochre), silica, kaolin, gelatin powder, Japanese paper
(9.6 g/m2), poly(ethyl methacrylate/methyl acrylate) [p(EMA/MA)],
Paraloid B72, pellets, and cellulose powder (Arbocel BC200, J. Rettenmaier
& Sohne, Gmbh) were purchased from Zecchi, Florence. Soluble starch,
cement, olive oil, mineral oil, and white spirit were commercially
available and thus purchased in non-specialized stores.
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3

Hydrogel Preparation and Characterization

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H-PVA (polyvinyl alcohol with hydrolysis
degree, HD, 98% and Mw 160 kDa), L-PVA
(polyvinyl alcohol with HD 88% and Mw 100
kDa), and PVP (polyvinyl pyrrolidone, Mw 1300 kDa) for the hydrogel preparation were purchased from Sigma-Aldrich.
Water for the hydrogels preparation was purified through a Millipore
system (resistivity > 18 MΩ cm). The following fluorescent
dyes
were used in CLSM or FCS calibration/measurements: fluorescein isothiocyanate
isomer I (FITC, purity ≥ 90%, Sigma-Aldrich); rhodamine B isothiocyanate
(RBITC, mixed isomers, Sigma-Aldrich); rhodamine 110 chloride (purity
≥99%, Sigma-Aldrich); Alexa Fluor 568 (Thermo Fisher Scientific).
The tartrazine (Dye content ≥ 85%, Sigma-Aldrich) was used
in the dye uptake, diffusion kinetics, and cleaning test experiments.
All the chemicals were used as received, without further purification.
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4

Optofluidic Device Beam Characterization

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A beam profiler camera (WinCamD-UHR–½ in. CMOS Beam Profiler; DataRay) was used to characterize the output beam of the laser. Optical characterization of the optofluidic device was carried out with a Rhodamine fluorescent dye (Rhodamine 110 chloride, Sigma-Aldrich). To measure the thickness of light-sheet, the add-on device was placed on the inverted microscope in top-view orientation [Fig. 1(c), right image], Rhodamine solution was pumped into the microchannel, and the fluorescent expression was imaged. Imaging resolution of the system was determined from SPIM images of 500-nm fluorescent beads (FP-0556-2, fluorescent Nile red particles, Spherotech). The beads were diluted in aqueous solution and continuously imaged as they flowed through the stationary light-sheet. The experimental lateral and axial resolutions of the system were assessed by analyzing the acquired consecutive frames of passing beads.
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