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363 fluorescence detector

Manufactured by Agilent Technologies
Sourced in United States

The 363 fluorescence detector is a lab equipment product manufactured by Agilent Technologies. It functions as a sensitive detector for fluorescence-based analysis.

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2 protocols using 363 fluorescence detector

1

Synthesis and Characterization of Gd(III) Contrast Agent

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Unless otherwise noted, materials and solvents were obtained from commercial suppliers and used without further purification. All reactions were performed under an inert nitrogen atmosphere. EMD 60F 254 silica gel plates were used for thin layer chromatography and visualized using UV light or ninhydrin stain. Column chromatography was performed using standard grade 60 Å 230 – 400 mesh silica gel (Sorbent Technologies). 1H NMR and 13C NMR spectra were obtained at room temperature on a Bruker Avance III 500 MHz NMR spectrometer. An Agilent 6210 LC-TOF spectrometer was used to acquire electro spray ionization mass spectra (ESI-MS). Matrix-Assisted Laser Desorption Ionization Time-Of-Flight (MALDI-TOF) mass spectrometry was carried out using a Bruker Autoflex III MALDI. Semi-preparative HPLC was performed on a Waters 19 × 250 mm X bridge C18 Column. Analytical HPLC was performed using a Waters 4.6 × 250 mm 5 μM X bridge C18 column using the Varian Prostar 500 system equipped with a Varian 363 fluorescence detector, and a Varian 335 UV/Vis Detector.
The amine functionalized Gd(III) scaffold (4) was synthesized according to literature procedure.30 For a detailed synthetic procedure of the peg functionalized scaffold (3) and the isothiocyanate functionalized dye (5) see the supporting information.
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2

Amino Acid Profiling of Yogurt Samples

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The yoghurt samples were pre-treated to remove proteins, and free amino acids were extracted as described by Simova et al. (2006) (link). The amino acid content of the samples was analysed using HPLC fitted with a sodium cation exchange amino acid analysis column (4×150 mm, Pickering, USA) and an o-phthaladehyde post-column derivation system (Pickering, USA). The equipment was coupled with a Waters 510 pump, a 7725i manual injector and a 363-fluorescence detector (Varian Inc, USA). The operating conditions used a flow rate of 1.7 mL/min. Elution was performed by applying a linear gradient of 100% solution A over 1 min, followed by 0-100% solution B over the subsequent 48 min (solution A, 0.2 mol/L sodium citrate, pH = 3.0; solution B, 0.2 mol/L sodium borate, pH = 9.8). The excitation and emission wavelengths were 338 nm and 425 nm, respectively.
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