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57 protocols using lc ms grade solvents

1

Quantitative Comparison of Monoclonal Antibodies

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Trastuzumab and Bevacizumab drug products were kindly provided from a Hospital Pharmacy Unit. The NIST monoclonal antibody (NISTmAb, lot number 14HB-D-002) reference material, RM 8671 (2.4 mg mL−1) was purchased from The National Institute of Standards and Technology (NIST). Thermo Scientific™ SMART Digest™ kits, magnetic resin option, were obtained from Thermo Fisher Scientific. LC-MS-grade solvents (0.1% (v/v) formic acid in water, 0.1% (v/v) formic acid in acetonitrile, formic acid, acetonitrile, water) were sourced from Fisher Scientific. Tris(2-carboxyethyl)phosphine hydrochloride (TCEP) and guanidine-HCl were obtained from Pierce. All other reagents were purchased from Sigma-Aldrich.
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2

Analytical Workflow for Quantitative LC-MS

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Screwcap cryovials (1.5 mL) were purchased from Sigma-Aldrich. Aeris 2.6 μm Peptide XB-C18 100 LC column 150 × 4.6 mm, Security guard Ultra Holder, Security guard Ultra Cartridges were purchased from Phenomenex (Torrance, CA). Chemglass Life Sciences 25 mL Tube, Storage, 14/20 Outer Joint, Airfree, Schlenk tube and 2 mL Filter Funnel, Buchner, Fine Frit were purchased from Thermo Fisher Scientific (Waltham, MA). All reagents and mobile phases were LC-MS-grade solvents purchased from Thermo Fisher Scientific (Waltham, MA) unless otherwise specified. MS grade water was produced in-house by a Millipore Milli-Q purification system with an LC-Pak Polisher filter for ultrapure water used for HPLC and LC-MS (Darmstadt, Germany). A more detailed list of reagents is in Supplemental Methods.
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3

Analytical Reagent Preparation for Plant Studies

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Analytical grade solvents (ethanol, isopropanol, hydrochloric acid, phosphoric acid) were supplied by ChemSupply, Australia. LC–MS grade solvents (acetonitrile and formic acid) were acquired from Thermo Fisher Scientific, US. Deionized water was used during plant growth experiments, whereas Milli-Q water (Merck Millipore, Germany) was used for all analytical processes. Formulation of Hoagland solution is supplied in Additional file 1.
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4

RNA Extraction and Quantification

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Unless otherwise stated, chemical reagents were purchased from Sigma‐Aldrich, Purelink RNA extraction kits were purchased from Life Technologies, LC‐MS grade solvents from Thermo Fisher, and RNA and DNA oligonucleotides from Integrated DNA Technologies.
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5

Isolation and Characterization of Ginger Compounds

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6S, 8S,
and 10S were purified from ginger
extract in our laboratory.10 (link) M2 was synthesized
in our laboratory, as previously reported.13 (link) HPLC-grade solvents and other reagents were obtained from VWR International
(South Plainfield, NJ). LC/MS grade solvents and other reagents were
obtained from Thermo Fisher Scientific (Rockford, IL). Glutathione
was obtained from Sigma-Aldrich (St. Louis, MN). Crystal violet, glutaraldehyde,
MTT [3-(4,5-dimethylthiaxol-2-yl)-2,5-diphenyltetrazolium bromide],
and propidium iodide were procured from Thermo Fisher Scientific (Waltham,
MA). Primary antibodies against β-actin, B-cell lymphoma 2 (Bcl-2),
caspase 9, caspase 3, cytochrome c, PUMA (p53 up-regulated
modulator of apoptosis), p53, XIAP (X-linked inhibitor of apoptosis
protein), as well as secondary antibodies conjugated to HRP (horseradish
peroxidase) against mouse and rabbit were purchased from Cell Signaling
Technology (Beverly, MA).
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6

Enzymatic Synthesis of Theaflavins

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TF was synthesized in house from the reaction between epicatechin (EC) and epigallocatechin (EGC) in the presence of POD and hydrogen peroxide (H2O2) according to our previous procedure.[2 (link)] Ammonium hydroxide solution, H2O2 (35%), MGO solution (40% in water), and type II POD from horseradish were purchased from Sigma (St. Louis, MO). Deuterated methanol (CD3OD) solvent was purchased from Acros Organics (now Thermo Fisher Scientific, Waltham, MA). Other common chemicals and solvents were purchased from VWR International (Radnor, PA). LC-MS-grade solvents were obtained from Thermo Fisher Scientific (Waltham, MA).
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7

Quantitative Crosslinking Mass Spectrometry Protocol

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Disuccinimidyl sulfoxide (DSSO), formic acid, dimethyl sulfoxide (DMSO), and LC–MS grade solvents were obtained from Thermo Scientific. Bovine serum albumin (BSA), (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), sodium chloride, magnesium chloride, potassium chloride, sucrose, ethylenediaminetetraacetic acid (EDTA), dithiothreitol, guanidinium hydrochloride, Staphylococcus aureus micrococcal nuclease, iodoacetamide, ammonium bicarbonate and formic acid were obtained from Millipore Sigma. Protease inhibitors 4-(2-aminoethyl)-benzenesulfonyl fluoride hydrochloride (AEBSF) and pepstatin were obtained from Santa Cruz, bestatin from Alfa Aesar, and leupeptin from EMD Millipore. Trypsin and GluC proteases were obtained from Promega. Chymotrypsin protease was obtained from Pierce Thermo. LysC was obtained from Wako Pure Chemical Industries.
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8

Comprehensive Mass Spectrometry Protocol

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LC-MS grade solvents (water,
acetonitrile, and isopropanol), formic acid (FA), and trifluoroacetic
acid (TFA) were purchased from Thermo Fisher Scientific (Waltham,
MA) or Merck (Darmstadt, Germany). Trypsin and trypsin/Lys-C proteases
(MS grade) were from Promega (Madison, WI); RapiGest detergent was
from Waters (Eschborn, Germany), and other common chemicals were from
Sigma-Aldrich (Munich, Germany). Polyacrylamide gradient gels (4–20%)
were from Serva Electrophoresis GmbH (Heidelberg, Germany). Protein
standards, glycogen phosphorylase (GP), alcohol dehydrogenase (ADH),
enolase (ENO), and ubiquitin (UBI), were purchased as a lyophilized
powder from Sigma-Aldrich. The reference protein standard (BSA, Pierce
grade, in ampules) was from Thermo Fisher Scientific (Waltham, MA).
Isotopically labeled amino acids (13C6,15N4-l-arginine (R) and 13C6-l-lysine (K)) were purchased from Silantes GmbH
(Munich, Germany).
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9

Proteomic Sample Preparation Protocol

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Empore C18 SPE discs were obtained from 3 M (St. Paul, MN). LC–MS grade solvents (methanol, water, and acetonitrile (ACN)) and formic acid (FA) as well as phosphate-buffered saline (PBS), thioUrea, tris(2-carboxyethyl)phosphine (TCEP), Gibco penicillin–streptomycin (P/S), and HeLa protein digest standard (P/N 88328) were products of Thermo Fisher Scientific (Waltham, MA). Urea, iodoacetamide (IAA), and trypan blue solution were purchased from Sigma-Aldrich (St. Louis, MO). Lysyl endopeptidase (Lys-C) was obtained from Wako Chemicals (Richmond, VA). Trypsin Gold was purchased from Promega (Madison, WI). Ammonium bicarbonate (ABC) was from Honeywell Fluka (Charlotte, NC). The RPMI 1640 medium with l-glutamine was a product of Corning (Corning, NY). Premium fetal bovine serum (FBS) was obtained from R&D Systems (Minneapolis, MN).
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10

Targeted Metabolomic Analysis Protocol

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All unlabeled standards and pyridine were ordered from Millipore-Sigma (St. Louis, MO, USA). Labeled standards ([U-13C2]-glycine, [U-13C6]-glucose, [U-13C4]-fumarate, and 13C-benzoic acid) were ordered from Cambridge Isotope Laboratories, Inc (Tewksbury, MA, USA). LC-MS grade solvents (chloroform, methanol, acetonitrile) and N-Methyl-N-(trimethylsilyl) trifluoroacetamide with 1% trimethylchlorosilane (MSTFA + 1% TMCS) were obtained from Thermo Fisher Scientific (Waltham, MA, USA). All chemicals used were analytical grade unless stated otherwise.
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