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Qm 40

Manufactured by Horiba
Sourced in Japan

The QM-40 is a laboratory equipment manufactured by Horiba. It is a versatile instrument that can be used for various analytical applications. The core function of the QM-40 is to measure and analyze materials using a scientific technique.

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6 protocols using qm 40

1

Pyrene Probe for Polymer Self-Assembly

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The self-assemblies of polymer cross-linkers in a pre-gelled solution were investigated using a pyrene probe. [14 (link),15 (link)]. The pyrene (Sigma, Peabody, MA, USA) was dissolved in acetone to prepare a stock solution with a concentration of 6.0 × 10−4 M. Polymer cross-linker pre-gelled solutions were prepared in DI (deionized) water (2 mL) by poly(ethylene glycol) diacrylate of Mn 575 g/mol (PEGDA-575, Sigma) and Mw 3400 g/mol (PEGDA-3400, Sigma), respectively. In parallel, acrylate group-free poly(ethylene glycol) of Mn 3350 g/mol (PEGdiol, Sigma) were dissolved in DI water as a control. Then, the pyrene solution was dropped into the polymer solutions with varying polymer concentrations. The mixture of the polymer solution and pyrene was sonicated for 10 min to ensure dispersion of pyrene in the polymer solution. The mixture was further incubated at room temperature for at least 12 h in the dark, so the pyrene was preferentially associated with hydrophobic domains of polymers. The mixture loaded in a quartz cuvette was excited at a wavelength of 330 nm and a resulting emission spectrum was obtained using photo luminescence (QM40, Photon Technology International, HORIBA, Japan). The band-width was adjusted to 2.0 nm for both excitation and emission.
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2

Comprehensive Materials Characterization Protocol

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HRTEM images were obtained on JEM 3010 high resolution transmission electron microscope. Field-Emission Scanning Electron Microscope (Carl Zeiss, SUPRA 55VP) was used to obtain SEM images and EDS analysis. Emission spectra were obtained on QM-40 (Photon Technology International, Inc.). A micro-Raman system (JY-Horiba, LabRam 300) was utilized for Raman spectrum recording with the 514.5 nm laser line from a Ar ion laser (Melles Griot, 35-MAP-321) for Raman excitation. Fluorescence images were obtained on Olympus X81 microscope coupled to an Andor LucaEMS 658 M camera. Zeta potential was measured on NanoPlus-1 (Particulate Systems).
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3

Fluorescence Titration of ZO NPs

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A steady-state spectrofluorimeter
(QM-40, Photon Technology International, PTI) connected by a xenon
lamp (150 W) as an excitation source was employed for fluorescence
titrations. Bare ZO NPs and the composite in the presence of different
DNAs were excited at 345 nm, and Hoechst 33258 was excited at 341
nm.
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4

Optimized Fluorescence Measurement Protocol

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All the fluorescence measurements were taken in the photon technology international (PTI) quanta master spectrofluorometer (QM-40), which is equipped with Peltier for controlling the temperature. Different parameters of the fluorometer, such as excitation and emission slit width, voltage, excitation and emission wavelength, etc., were optimized, along with the volume of mixture, incubation temperature, and time; the following standardised parameters were used for all the measurements:

Excitation slit width: 1.25 mm

Emission slit Width: 1.25 mm

Voltage: 121 V

Integration time: 0.1 s

Excitation wavelength: 495 nm

Emission range: 505–650 nm

Maximum emission wavelength: 519 nm

Volume of the mixture: 20 µL

Incubation temperature: 50 °C

Incubation time: 15 min

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5

Organic Photoluminescence Characterization

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Solution samples were prepared with toluene at a concentration of 0.01 mM. The neat film was deposited on quartz at a rate of 1 angstrom per second under vacuum. The UV-Vis absorption spectrum was obtained using a Lambda 1050 UV/Vis/NIR spectrometer (PerkinElmer). Photoluminescence (PL) spectra were recorded using the Photon Technology International QM-40. Absolute photoluminescence quantum yield (PLQY) and transient quantaurus-QY (Hamamatsu) were obtained. The low-temperature photoluminescence spectrum was measured at 77 K using the Jasco FP-6500. Photoluminescent decay traces were obtained through time-correlated single-photon coefficient (TCSPC) technology using PicoQuant, FluoTime 250 instruments (PicoQuant, Germany). A 377 nm pulse laser was used as an excitation source and data analysis was performed using the exponential fitting model of the FluoFit software.
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6

Actin Nucleation Assay Protocol

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Both rabbit muscle actin (RMA) and pyrene actin were mixed to prepare 12 μM 10% pyrene actin in G-Buffer. This mixture was incubated for 2 minutes at room temperature with MgCl 2 and EGTA. Different concentrations of the desired protein were added and the volume was adjusted with G-buffer and HEKG5. Just prior to polymerization reaction, 20X Initiation Mix (1 M KCl, 40 mM MgCl2, 10 mM ATP) was added. Fluorescence was measured at 365 nm (excitation) and 407 nm (emission) wavelength at 25ºC in fluorescence spectrophotometer (QM40, Photon Technology International, Lawrenceville, NJ) [22] . Actin nucleation assay was repeated five times.
was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission.
The copyright holder for this preprint (which this version posted December 11, 2016. ; https://doi.org/10.1101/093104 doi: bioRxiv preprint
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