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Agilent 8453 uv vis

Manufactured by Agilent Technologies
Sourced in United States

The Agilent 8453 UV-Vis is a spectrophotometer designed for ultraviolet-visible absorption measurement. It features a diode array detector and a wavelength range of 190 to 1100 nanometers.

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3 protocols using agilent 8453 uv vis

1

Spectrophotometric Quantification of Propolis Phenolics

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The total amount of phenolic compounds in propolis extracts was determined spectrophotometrically using the Folin-Ciocalteu method [16 (link)] with slight modifications. Every investigated extract (0.5 ml) was mixed with 2 N 0.5 ml of Folin-Ciocalteu reagent for 6 min. After the addition of 1.5 ml 20% Na2CO3, the volume was made up to 10 ml with corresponding extraction solvents, followed by incubation for 2 h at room temperature. Absorbance of the mixture was measured at 765 nm using spectrophotometer Agilent 8453 UV-Vis (Agilent Technologies Inc., Santa Clara, USA). Total phenolic compounds content was calculated from the calibration curve of p-coumaric acid and expressed as milligram of p-coumaric acid equivalents per ml of propolis extract.
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2

Photoabsorber Absorbance Measurement

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Absorbance measurement was performed by using an Agilent 8453 UV-Vis (Agilent technologies, Santa Clara, CA, USA). After mixing 1% (v/v) photoabsorbers of various colors (Red, Orange, Yellow, Green, Blue, Purple, and Pink) in DPBS with 0.5% (w/v) LAP, the samples were placed in a cuvette and measured. The blank group did not contain any photoabsorber.
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3

Preparation of AS-IgG1 Protein Solutions

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Amgen provided AS-IgG1 at a stock concentration of 30 mg/mL. 5 mM citrate buffer solutions were prepared using MilliQ distilled deionized water (Millipore, Billerica, MA), citric acid monohydrate (Fisher Scientific), and sodium chloride (Fisher Scientific). The solution pH was adjusted using sodium hydroxide (Fisher Scientific). Protein solutions were dialyzed against the desired buffer as previously described [12 (link)]. After dialysis, solutions were filtered with 0.22 μm filters (Millipore), and the concentration was determined from the absorbance at 280 nm using a UV-vis spectrophotometer (Agilent 8453 UV-Vis, Agilent Technologies, Santa Clara, CA) using the AS-IgG1 extinction coefficient of 1.586 mL/mg cm. All solutions were diluted gravimetrically to final AS-IgG1 concentrations of 1 mg/mL.
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