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Accela 80 hz

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Accela 80 Hz is a high-performance liquid chromatography (HPLC) system designed for analytical applications. It features an 80 Hz data acquisition rate, allowing for rapid and precise measurements of sample components. The Accela 80 Hz is capable of delivering a wide range of flow rates and operating pressures, making it suitable for a variety of HPLC methods and applications.

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2 protocols using accela 80 hz

1

HPLC-MS Analysis of Natural Lipid Extracts

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NLEs were analyzed using a high-performance liquid chromatography (HLPC) system with a PDA Detector (Accela 80 Hz) and an LTQ-Velos ion trap mass spectrometer fitted with a heat electrospray ionization interface (Thermo Fisher Scientific, Waltham, MA, USA) with a C18 column (1.9 µm, 2.0 × 100 mm, UPLC BEH C18, Waters, USA). The elution gradient was carried out with a binary solvent system consisting of 0.1% formic acid in water (solvent A) and 0.1% formic acid in acetonitrile (solvent B) at a constant flow rate of 0.3 ml/min. The linear gradient profile was as follows: 5-10% solvent B over 5 min, 10% solvent B for 10 min, 10-40% solvent B over 30 min, 40-90% solvent B over 40 min, then returned to 5% solvent B over 5 min, followed by conditioning for 10 min, finished at 55 min. Acquisition was performed in the negative and positive ion modes using electrospray ionization. The capillary temperature was 275℃, with sheath gas at 35 units and auxiliary gas at 5 units. NLEs were run in triplicate and the collected data was processed for profiling and identification.
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2

Phloroglucinolysis Method for Proanthocyanidin Analysis

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The PAC’s mDP and %Gal were determined following the phloroglucinolysis method described by Kennedy et al. [31 (link)] with slight modifications. Briefly, 10 to 100 mg of sample, depending on PAC concentration, were dissolved in 1.0 mL of a freshly prepared methanol solution containing 50 g/L of phloroglucinol, 10 g/L of ascorbic acid, and 0.1 M of hydrochloric acid. Insolubilized material was removed by centrifugation, after which 400 µL of the supernatant were transferred to pressure resistant vials and incubated at 50 °C for 1 h followed by the addition of 2 mL of 40 mM sodium acetate aqueous solution to stop the reaction. Depolymerization products were quantified by high performance liquid chromatography (HPLC) in a Accela 80 Hz (Thermo Fisher Scientific, San Jose, CA, USA) (Figure S1 in Supplementary Materials) and peak attribution was made by electrospray ionisation mass spectrometry (ESI-MS) in a LCQ Fleet ion trap mass spectrometer (ThermoFinnigan, San Jose, CA, USA) (Table S1 in Supplementary Materials) operated as described elsewhere [32 (link)]. mDP was calculated by dividing the sum of terminal and extension units by the sum of terminal units and the %Gal was calculated by dividing the sum of galloylated units by the sum of all units.
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