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Sunfire c18 rp

Manufactured by Waters Corporation

The SunFire C18 RP is a reversed-phase high-performance liquid chromatography (HPLC) column designed for the separation and analysis of a wide range of compounds. It features a silica-based stationary phase with a C18 alkyl ligand. The column provides efficient and reliable separation performance for both polar and non-polar analytes.

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4 protocols using sunfire c18 rp

1

LC-HRESIMS Analysis of Natural Compounds

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The following conditions were used for LC-HRESIMS analysis: capillary voltage 45 V, capillary temperature 260 °C, auxiliary gas flow rate 10–20 arbitrary units, sheath gas flow rate 40-50 arbitrary units, spray voltage 4.5 kV, and mass range 100–2000 amu (maximum resolution 30000). Gradient separation was achieved while using a SunFire C18 RP analytical HPLC column (5µm, 4.6 × 150 mm, Waters) with a mobile phase of 0–100% MeOH over 30 min. at a flow rate of 1 mL/min. Multiple available databases (SciFinder: https://sso.cas.org/as/E9dPQ/resume/as/authorization.ping, MarinLit: http://pubs.rsc.org/marinlit/, Dictionary of Natural Products: http://dnp.chemnetbase.com/faces/chemical/ChemicalSearch.xhtml, PubChem: https://pubchem.ncbi.nlm.nih.gov/, Chemspider: http://www.chemspider.com/) were used for the dereplication and annotation of known compounds.
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2

LC-HRESIMS Spectrometric Technique

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LC-HRESIMS spectrometric technique is composed of Thermo Instruments MS system (LTQ XL/LTQ Orbitrap Discovery) coupled to a Thermo Instruments HPLC system (Accela PDA detector, Accela PDA autosampler and Accela Pump). The following conditions were used: capillary voltage 45 V, capillary temperature 260°C, and auxiliary gas flow rate 10–20 arbitrary units, sheath gas flow rate 40–50 arbitrary units, spray voltage 4.5 kV, mass range 100–2000 amu (maximum resolution 30000). For LC/MS; Waters SunFire C18 RP analytical HPLC column (5 μm, 4.6 × 150 mm) using a gradient of MeOH in H2O containing 0.01% formic acid as eluent (0–100% over 30 min) at a flow rate 1 mL/min. (Marine Biodiscovery Centre, Chemistry Department, University of Aberdeen).
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3

ESI-MS Analysis of Fungal Metabolites

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ESI-MS was performed for the sample from the 300 μM SA-treated fungal culture filtrate. Thermo Scientific MS system (XL/LTQ Orbitrap Discovery) coupled with a Thermo Scientific HPLC system (Accela PDA detector/autosampler/pump) was used. The following conditions were maintained in LC-MS analysis: capillary voltage 45 V, capillary temperature 260°C, auxiliary gas flow rate 10–20 arbitrary units, sheath gas flow rate 40–50 arbitrary units, spray voltage 4–5 kV and a mass range of 100–2000 amu (maximum resolution 30,000). Gradient separation was used on a Waters SunFire C18 RP analytical HPLC column (100Å, 5 μm, 4.6 mm × 150 mm) with a mobile phase of 0–100% MeOH over 30 min at a flow rate of 1 mL min-1.
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4

Quantitative Mass Spectrometry Proteomics

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Total proteins were analyzed by liquid chromatography/mass spectrometry using a Thermo Instruments MS system (LTQ XL/LTQ Orbitrap Discovery) coupled to a Thermo Instruments HPLC system (Accela PDA detector, Accela PDA autosampler, and Accela pump) TUV Rheinland of North America Inc with Waters Sun Fire C18 RP analytical HPLC column (5 μm, 4.6 × 150 mm) as described (11 (link), 15 (link)). Metabolites molecular formulas were deducted by exact mass of eluted peaks, and identified in Dictionary of Natural Products, CRC press, online version for matching expected compounds.
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