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Easy spray nanoesi

Manufactured by Thermo Fisher Scientific
Sourced in United States

The EASY-Spray nanoESI is a laboratory instrument designed for nanospray electrospray ionization (nanoESI) applications. It provides a reliable and consistent method for sample introduction into mass spectrometers. The core function of the EASY-Spray nanoESI is to generate a stable and reproducible electrospray of sample solutions for mass spectrometry analysis.

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2 protocols using easy spray nanoesi

1

Protein Extraction and Quantification

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Tissue homogenization and sonication were carried out by means of a Wheaton® 903475 Overhead Stirrer apparatus (Wheaton, Millville, NJ, USA) and a Branson Sonifier 450 (Branson Ultrasonics, Danbury, CT, USA), respectively. Total protein concentration was determined in duplicate by Bradford assay (Bio-Rad Laboratories, Hercules, CA, USA) and UV–Vis spectrophotometer (8453 UV–Vis Supplies, Agilent Technologies, Waldbronn, Germany) detector using BSA as the protein of reference. For sample centrifugation, a thermostated centrifuge SL16 R (Thermo Fisher Scientific, Langenselbold, Germany) or Mini Spin (Eppendorf AG, Hamburg, Germany) were used as specified for sample treatment. HPLC–ESI–MS/MS analyses were performed on an UltiMate 3000 RSLCnano System (Dionex, Sunnyvale, CA, USA) coupled with an Orbitrap Elite MS detector with ESI or EASY-Spray nanoESI sources (Thermo Fisher Scientific), as specified elsewhere.
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2

Proteomic Analysis of Tissue Samples

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Tissue homogenization and sonication were carried out by means of Wheaton® 903475 Overhead Stirrer apparatus (Wheaton, Millville, NJ, USA) and Branson sonifer 450 (Branson Ultrasonics, Danbury, CT, USA), respectively. Total protein concentration was determined in duplicate by Bradford assay (Bio-Rad Laboratories, Hercules, CA, USA) and UV-Vis spectrophotometer (8453 UV-Vis Supplies, Agilent Technologies, Waldbronn, Germany) detector using BSA as the protein of reference. For sample centrifugation, thermostated centrifuge SL16 R (Thermo Fisher Scientific, Langenselbold, Germany) and Mini Spin (Eppendorf AG, Germany) were used as specified for sample treatment. HPLC-ESI-MS/MS analyses were performed on UltiMate 3000 RSLCnano System (Dionex, Sunnyvale, CA, USA) coupled to Orbitrap Elite MS detector with ESI or EASY-Spray nanoESI sources (Thermo Fisher Scientific), as specified elsewhere.
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