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Aminco bowman series 2

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Aminco-Bowman Series 2 is a luminescence spectrometer designed for spectroscopic analysis. It is capable of measuring fluorescence, phosphorescence, and bioluminescence.

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2 protocols using aminco bowman series 2

1

Characterization of Amino Acids and Peptides by MALDI-TOF MS

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Mass spectra were recorded using AXIMA CFR MALDI-TOF Mass Spectrometer from Kratos Analytical Ltd. (Manchester, UK), equipped with a nitrogen laser (337 nm). The laser energy was selected from 0 to 180 a.u. (arbitrary units). The repetition mode of experiments was performed at a frequency of 5 Hz and a pulse time width of 3 ns. Analyses were carried out in linear/reflectron positive/negative ion modes. Generally, MALDI-TOF MS of amino acids and peptides is usually measured in the positive ion mode, therefore, the study was performed in the positive ion mode. The irradiated spot size was about 150 µm in diameter and the maximum laser power was 6 mW (180 a.u.). The resulting laser energy fluence was ~ 1 J/cm2.
UV–Visible spectra were measured using a UV mini-1240 spectrophotometer from Shimadzu Corporation (Kyoto, Japan). A spectrofluorometer Aminco-Bowman Series 2 (Thermo Fisher Scientific, MA, USA) equipped with a 150 W Xe lamp was used. Excitation wavelength was set at 445 nm and emission wavelength was set at 525 nm. The spectra were acquired with 1 nm resolution and a scanning speed of 1 nm/s. A MiniSpin Plus of Eppendorf (Hamburg, Germany) centrifuge machine was used for centrifugation.
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2

Quantification of Caffeine and Labeled Compounds in Acceptor Phases

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The concentration of caffeine (0.2 kDa) in the samples of the acceptor phase was assessed using HPLC (Agilent 1200 equipped with UV/VIS and FLD detectors, Agilent, USA). The amount of caffeine was determined using a Zorbax Eclipse plus C18 column (250 x 4.6 mm, 5 μm) and methanol:0.2% aqueous solution of formic acid 1:3 (v/v) as the mobile phase with the flow rate 1.5 mL/min. The UV/VIS detector wavelength was set at 272 nm. The retention time of caffeine peak was 5.75 min. Spectrofluorimetric quantification of fluorescently labelled dextrans (FD4, FD20, FD40 and FD70) in samples of the acceptor phase was carried out on Aminco Bowman Series 2 (ThermoFisher, USA). The excitation wavelength was set at 419 nm and emission wavelength at 529 nm. The system was calibrated using the individual dextran standards dissolved in acceptor buffer pH 7.4. Spectrofluorometric quantification of fluorescently labelled bovine serine albumin FITC-BSA (66 kDa) in samples of the acceptor phase was carried out on Agilent 1200 HPLC with FLD detector using a column bypass (Agilent Technologies, USA). The excitation wavelength was set at 495 nm and emission wavelength at 523 nm. The system was calibrated using standard FITC-BSA solutions in acceptor buffer pH 7.4.
All HPLC data were analysed using Agilent ChemStation software Rev.C.01.06 (Agilent Technologies, USA).
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