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Continuous flow liquid helium cryostat

Manufactured by Oxford Instruments

The continuous-flow liquid helium cryostat is a specialized laboratory equipment designed to maintain extremely low temperatures for research and experimentation purposes. It uses a continuous flow of liquid helium to provide a stable, controlled environment for studying materials and phenomena at cryogenic temperatures.

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4 protocols using continuous flow liquid helium cryostat

1

Photoluminescence and Microscopy Characterization

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Photoluminescence
measurements were performed on an Edinburgh Instruments FLS920 spectrometer
equipped with a TMS300 monochromator, 450 W Xe lamp, thermoelectrically
cooled Hamamatsu R928 PMT detector, and a liquid N2 cooled
R5509-72 NIR PMT for wavelengths beyond 825 nm. The recorded emission
spectra were corrected for the spectral responsivity of the detectors
and monochromators. Photoluminescence decay curves were recorded with
a pulsed Coherent 45 mW OBIS LX 445 nm laser (modulated with an Agilent
function generator) and an R5509-72 NIR PMT. Cryogenic measurements
were performed in a continuous-flow liquid helium cryostat from Oxford
Instruments. UV/Vis absorption spectra were measured on a PerkinElmer
950 UV/vis/NIR spectrophotometer. Transmission electron microscopy
(TEM) samples were made by drop-casting a diluted dispersion of NCs
on carbon-coated TEM copper grids. Bright-field (BF-TEM) and high-angle
annular dark-field scanning transmission electron microscopy (HAADF-STEM)
images were taken on a Talos F200X from FEI operating at 200 keV.
High-resolution HAADF-STEM imaging was performed on an aberration-corrected
Titan electron microscope from Thermofisher operating at 300 keV.
To minimize structural changes of NCs during imaging, a low beam current
of ∼5 pA was used with relatively low magnifications.
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2

Kinetic EPR Study of Enzyme Reaction

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X-band EPR spectra were recorded on a Bruker Elexsys 500 spectrometer equipped with an Oxford Instrument continuous-flow liquid helium cryostat and a temperature control system.
A series of samples of 1 (50 μM) was mixed with HRP and H 2 O 2 in buffer pH 8.1 as indicated in Section 2.1, transferred in quartz tubes and incubated for different times (1, 2, 5, 10 min). At the end of the incubation the tubes were frozen in a liquid nitrogen bath and introduced in the EPR cavity. EPR experiments were performed at 10 K, using a microwave power of 0.159 mW (non saturating conditions) with a modulation of 1 G.
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3

EPR Spectroscopy of MrpORP_CT

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The EPR spectra of 0.1 mM MrpORP_CT, in 100 mM Tris-HCl, 500 mM NaCl, 3 mM DTT pH 8.1, were recorded on a X-band Bruker EMX spectrometer equipped with a rectangular cavity (model ER 4102 T) and an Oxford Instruments continuous liquid helium flow cryostat. The EPR sample was reduced with a solution of sodium dithionite prepared in 100 mM Tris-HCl pH 7.6. The experimental conditions used for spectral acquisition are described in the Figure legend. The EPR samples were prepared under anoxic conditions either inside a COY or a Mbraun anaerobic chamber.
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4

Spectroscopic Characterization of Laz Protein

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The visible-spectra were recorded on a Shimadzu UV-1800 spectrophotometer using 1 cm quartz cells. Laz samples were oxidized with a solution of potassium ferricyanide and reduced with a solution of sodium ascorbate.
The Laz sample for EPR was 0.3 mM in 20 mM phosphate buffer, pH 7.0. The EPR spectra of Laz were recorded on a X-band Bruker EMX Fig. 1. Analysis of the primary sequence of Ng Laz. In green underlined is the signal peptide recognized by the signal peptidase II pathway; in blue are identified the residues of the mature protein recognized by the epitope for the H.8 MAb; and in black the azurin-like domain.
spectrometer equipped with a rectangular cavity (model ER 4102T) and an Oxford Instruments continuous liquid helium flow cryostat. Experimental conditions are described in the legend of the spectrum. The simulation of the spectrum was performed using WINEPR SimFonia software version 1.2, from Bruker.
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