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6530 lc q tof system

Manufactured by Agilent Technologies
Sourced in United States

The 6530 LC/Q-TOF system is a liquid chromatography-quadrupole time-of-flight mass spectrometer designed for high-resolution, accurate-mass analysis. It combines liquid chromatography with a quadrupole and time-of-flight mass analyzer to provide precise mass measurements and extensive compound identification capabilities.

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2 protocols using 6530 lc q tof system

1

Electrochemical Characterization of CNT/CNC/AgNP

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Electrochemical measurements such as CV, differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS) were carried out with a BASi Palmsens-4 potentiostat (PalmSens B.V., Houten, The Netherlands). A three-electrode system was used for all electrochemical measurements, wherein an MN electrode, platinum wire, and in-house Ag/AgCl reference electrode (composition delineated vide infra) were used as the working, counter, and reference electrodes, respectively. To fabricate the in-house Ag/AgCl reference electrode, silylated needles were first infused with a homogenous suspension comprising 1 mg/mL of CNT, 4 mg/mL of CNC, and 5 mg/mL of AgNPs at a flow rate of 15 µL/min. The CNT/CNC/AgNP-modified needles were then immersed in 0.5% NaClO bleach at room temperature overnight, and rinsed with DI water. FTIR spectra were recorded using a Bruker Tensor 27 FTIR instrument fitted with diamond-attenuated total reflectance (ATR). Scanning electron microscope (SEM) images were acquired from a Zeiss Sigma 300 VP field emission SEM. The HPLC was performed by an Agilent 1260 II Analytical-Scale LC Purification System with 6530 LC/Q-TOF system (Agilent Technologies Inc., Santa Clara, CA, USA). Separation was performed on a Superlco® analytical Ascentis® C18 column (Sigma-Aldrich Inc., St. Louis, MI, USA, 15 cm × 2.1 mm, 3 µM).
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2

Analyzing V272M DBD-PAT Interaction by MS

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Protein buffer of V272M DBD was replaced by 200 mM ammonium acetate buffer (pH 7.0) using dialysis device. V272M DBD was mixed with PAT at a molar ratio of 1 : 1 and the mixture was divided into two same samples. The mass of the two samples were immediately determined, without an incubation step, by native MS and denatured MS, respectively. The mass of V272M DBD without PAT treatment was also determined in the same way. Native MS was carried out on a 1290 Infinity II LC coupled with a 6230 LC/TOF system equipped with an Agilent Jet Stream source. LC separation was obtained with PolyHYDROXYETHYL ATM column (200 3 2.1 mm, 5 mm, 200 A ˚). In denatured MS, a 1290 Infinity II LC coupled with a 6530 LC/QTOF system and an Agilent 300SB-C8 column (50 3 2.1 mm, 3.5 mm) were used for denatured protein determination. All experimental MS data of the samples were processed using Agilent MassHunter Qualitative Analysis 7.0 software. Experimental molecular weights (MW) were determined from MS peak maxima with average MW and standard deviations calculated from identified charge states.
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