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6 protocols using d4 cholic acid

1

Metabolomic Analysis of Plant Pathogen Infection

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Samples were prepared from control and infected 5-week-old plants47 (link). 20 mg of grinded samples were mixed with 1 mL extraction buffer (20/20/60 v/v/v chloroform:water:methanol) including internal standards for GC–MS and LC–MS. LC–MS internal standards were: 13C9-phenylalanine, 13C3-caffeine, D4-cholic acid, D8-arachidonic acid and 13C9-caffeic acid (Sigma, St. Louis, MO, USA). GC–MS internal standards were: L-proline-13C5, alpha-ketoglutarate-13C4, myristic acid-13C3, cholesterol-D7 (Cambridge Isotope Laboratories, Inc., Andover, MA, USA) and succinic acid-D4, salicylic acid-D6, L-glutamic acid-13C5,15N, putrescine-D4, hexadecenoic acid-13C4, D-glucose-13C6, D-sucrose-13C12 from Sigma. The samples were bead-beated and centrifuged as described27 (link). Most of the supernatants, 200 µL for LC–MS analysis and 50 µL for GC–MS analysis, were transferred to micro vials, evaporated to dryness and stored at − 80 °C until analysis. Small aliquots of the remaining supernatants were pooled and used as quality control (QC) samples. MSMS analysis (LC–MS) was run on the QC samples for identification purposes. The samples were analyzed in batches according to a randomized run order on both GC–MS and LC–MS.
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2

Metabolomic Analysis of Freeze-Dried Roots

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Freeze-dried root samples (5mg) were prepared according to the method (Gullberg et al., 2004) at the Swedish Metabolomics Center for metabolomics analysis. The samples were shaken with extraction buffer (1000 µL) in a mixer will with a tungsten bead at 30 Hz for 3 minutes. The samples were centrifuged at 14,000 rpm for 10 minutes (4 °C) after removing the bead. The supernatant (20 µL for amino acid quantification and 100 µL for LC-MS analysis) was transferred and evaporated to dryness in a speed-vac concentrator. Afterward, the samples were stored at -80 o C until further analysis. To ensure quality control (QC), a small aliquot of remaining supernatants was pooled and run on MSMS for identification purposes. The extraction buffer contained internal standards for LC-MS such as 13C9-Phenylalanine, 13C3-Caffeine, D4-Cholic acid, and 13C9-Caffeic acid that were obtained from Sigma (St. Louis, MO, USA).
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3

Lipidomic Analysis by AbsoluteIDQ p180 Kit

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The AbsoluteIDQ® p180 Kit was purchased from Biocrates Life Sciences AG, Innsbruck, Austria. All chemical standards of lipids were purchased from Aldrich-Fluka-Sigma S.r.l. (Milan, Italy). Labeled internal standards: D3-octanoyl L-carnitineHCl, D3-hexadecanoyl L-carnitineHCl, D3-acetyl L-carnitineHCl, D3-L-carnitine HCl, D3-eicosanoic acid, D3-octadecanoic acid (D3-stearic acid) and D3-tetradecanoic acid (D3-myristic acid) were from CDN Isotope (Quebec, Canada); D7-cholesterol, D4-cholic acid, D4-chenodeoxycholic acid, D4-glycoursodeoxycholic acid, D4-glycocholic acid, D5-taurocholic acid, D5-taurodeoxycholic acid, D4-lithocholic acid were from Sigma–Aldrich (Sigma–Aldrich, Milan, Italy). All chemicals had a purity grade greater than 90% and were used without further purification. Acetonitrile (ACN), 2-propanol (IPA), methanol (CH3OH), chloroform (CHCl3) and triethylamine (TEA) were purchased from Sigma–Aldrich (Sigma–Aldrich, Milan, Italy). All these solvents were of LC-MS grade, water was MilliQ (Millipore, Vimodrone, Milan, Italy). Formic acid (HCOOH) and ammonium formate (NH4COOH) additive for LC–MS were from FLUKA (Sigma–Aldrich, Milan, Italy).
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4

Analytical Chemistry Protocol for Metabolomics

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HPLC- or MS-grade solvents acetonitrile (ACN), methanol (MeOH), and chloroform (CHCl3) were purchased from Merck (Darmstadt, Germany) or Sigma-Aldrich (Steinheim, Germany or St. Louis, MO). MS grade water or ultrapure water was purchased from Merck (Darmstadt, Germany) or using a Milli-Q purity system (Millipore, Billerica, MA).
MeOH-dissolved internal standard solution (ISS-1) containing L-methionine sulfone, D-camphor-10-sulfonic acid sodium salt, leucine-d3, phenylalanine-d5, tryptophane-d5, succinic acid-13C4, and cholic acid-d4 (all from Sigma-Aldrich, Steinheim, Germany) was used to normalize signal intensity of the CE-TOF/MS data. ACN-dissolved ISS-2 consisting of N,N-diethyl-2-phenylacetamide, trimesic acid, disodium 3-hydroxynaphthalene-2,7-disulfonate (all from Wako, Japan), and 3-aminopyrrolidine dihydrochloride (Aldrich, St. Louis, MO) was used to adjust the migration time of the CE-TOF/MS analysis. Internal standards of free fatty acid (FFA) 16:0-d4 (Cambridge Isotope Laboratories, Tewksbury, MA, USA), and FFA 22:0-d4 (ten Brink laboratories, Amsterdam, Netherlands) dissolved in CHCl3/MeOH (2:1, v/v) were used to normalize signal intensity of the UHPLC-Q-TOF/MS-based FFA analysis.
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5

Biomarker Detection Protocol

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The standards of reserpine and cholic acid-d4 were purchased from Sigma Aldrich (St. Louis, MO, USA), betaine (97%) was purchased from TCI (Shanghai, China). HPLC grade acetonitrile was purchased from Merck & Co (Billerica, MA, USA). Ultrapure water was produced from a Milli-Q system (Millipore, MA, USA). The alanine transaminase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), and hydroxyproline detection kits were acquired from Nanjing Jiancheng Bioengineering Institute (Nanjing, China).
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6

Metabolite Quantification Protocol

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Internal standards, including lysophosphatidylcholine C19:0 (LPC 19:0), phosphatidylcholine C38:0 (PC 38:0), phosphatidylethanolamine C30:0 (PE 30:0), sphingomyelin C12:0 (SM 12:0), ceramide C17:0 (Cer 17:0), fatty acid C16:0-d3 (FA 16:0-d3), fatty acid C18:0-d3 (FA 18:0-d3) and triglyceride 45:0 (TG 45:0) were purchased from Avanti Polar Lipids (Alabaster, AL). Internal standards, including acetylcarnitine-d3 (carnitine C2:0-d3), carnitine C10:0-d3, carnitine C16:0-d3, tryptophan-d5, phenylalanine-d5, cholic acid-d4, chenodeoxycholic acid-d4) were purchased from Sigma company (US). Ammonium acetate and tert-butyl methyl ether (MTBE) were purchased from Sigma company (US). Acetonitrile, methanol and isopropanol were purchased from Merk company (German). Milli-Q water was made from a Milli-Q system (Millipore,Billerica,MA). Pyridine, methoxyamine hydrochloride, and N-Methyl-N-(trimethylsilyl) tri uoroacetamide (MSTFA) for GC-MS derivatization were obtained from Sigma-Aldrich (St. Louis, MO, USA).
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