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Avance dpx 300 ft nmr spectrometer

Manufactured by Bruker
Sourced in United States

The Avance DPX-300 FT-NMR spectrometer is a nuclear magnetic resonance (NMR) instrument designed for basic research and routine analysis. It operates at a magnetic field strength of 7.05 Tesla, providing a 1H NMR frequency of 300 MHz. The spectrometer is equipped with a superconducting magnet and features automated sample handling and data processing capabilities.

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7 protocols using avance dpx 300 ft nmr spectrometer

1

Spectroscopic Analysis and Enzyme Assays

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Optical rotations were obtained with a Perkin-Elmer 341 polarimeter (Boston, MA, USA). UV spectra were measured on a Milton Roy Spectronic 300 Array spectrophotometer, and IR was recorded on a Perkin-Elmer FT-IR 1760x spectrophotometer (Boston, MA, USA). High-resolution electrospray ionization mass spectra (HR-ESI-MS) were recorded with a Bruker micro TOF mass spectrometer (Billerica, MA, USA). NMR spectra were obtained with a Bruker Avance DPX-300 FT-NMR spectrometer (Billerica, MA, USA). Vacuum liquid chromatography (VLC) and column chromatography (CC) were performed on silica gel 60 (Merck, 70–230 µm, Darmstadt, Germany), silica gel 60 (Merck, 230–400 nm) or Sephadex LH-20 (Pharmacia, Piscataway, NJ, USA). Yeast α-glucosidase enzyme, p-nitrophenol-α-d-glucopyranoside, pancreatic lipase, and 4-methylumbelliferyl oleate were purchased from Sigma Chemical, Inc. (St. Louis, MO, USA), and acarbose from Fluka Chemical (Buchs, Switzerland).
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2

Spectroscopic Characterization of Compounds

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Optical rotations were determined with a PerkinElmer Polarimeter 341 (Boston, MA, USA). UV spectra were recorded on a Milton Roy Spectronic 3000 Array spectrophotometer (Rochester, Monroe, NY, USA). IR spectra were obtained with a PerkinElmer FT-IR 1760X spectrophotometer (Boston, MA, USA). Mass spectra were measured using a Bruker MicroTOF mass spectrometer (ESI-MS) (Billerica, MA, USA). NMR spectra were recorded on a Bruker Avance DPX-300FT NMR spectrometer or a Bruker Avance III HD 500 NMR spectrometer (Billerica, MA, USA). Yeast α-glucosidase enzyme and p-nitrophenol-α-d-glucopyranoside were obtained from Sigma Chemical, Inc. (St. Louis, MO, USA), and acarbose was purchased from Fluka Chemical (Buchs, Switzerland). Microtiter plate readings were carried out with a CLARIOstar apparatus (BMGLABTECH, Ortenberg, Germany).
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3

Spectroscopic Characterization of Cellular Oxidative Stress

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The Milton Roy Spectronic 3000 Array spectrophotometer (Rochester, Monroe, NY, USA) was used to record UV spectra, while IR spectra were obtained from the PerkinElmer FT-IR 1760X spectrophotometer (Boston, MA, USA). Mass spectra were determined using the Bruker MicroTOF mass spectrometer (ESI-MS) (Billerica, MA, USA). NMR spectra were recorded by the Bruker Avance DPX-300FT NMR spectrometer or the Bruker Avance III HD 500 NMR spectrometer (Billerica, MA, USA). Sigma Aldrich (Sigma-Aldrich, Dorset, UK) provided 2′,7′-dichlorofluorescein di-acetate (DCFH-DA), and Merck Millipore (Merck Millipore, Darmstadt, Germany) supplied fetal bovine serum (FBS). Invitrogen (Invitrogen Ltd., Paisley, UK) provided Dulbecco’s modified Eagle’s Medium/Nutrient Mixture F-12 Ham (DMEM/F-12), penicillin–streptomycin, H2O2, dimethyl sulfoxide (DMSO), and 3-[4,5-dimethyltiazol-2-yl]-2,5-diphenyl-tetrazolium bromide (MTT). Antibodies used in western blotting were obtained from Cell Signaling Technology (Danvers, MA, USA). Antioxidant enzyme assay test kits were obtained from Cayman Chemical (Cayman Chemical, Ann Arbor, MI, USA).
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4

Spectroscopic and Chromatographic Techniques

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UV spectra were recorded on a Milton Roy Spectronic 300 Array spectrophotometer (Rochester, Monroe, NY, USA), and IR spectra were obtained on a Perkin-Elmer FT-IR 1760X spectrophotometer (Norwalk, Fairfield, CT, USA). Optical rotation was measured on a Perkin-Elmer 341 polarimeter (Norwalk, Fairfield, CT, USA). Mass spectra were recorded on a Bruker micro TOF mass spectrometer (ESI-QqTOF-MS) (Manchester, UK). NMR spectra were recorded on a Bruker Avance DPX-300 FT-NMR spectrometer or a Bruker Avance III HD 500 NMR spectrometer (Rheinstetten, Germany). Column chromatography (CC) was performed on silica gel 60 (Kieselgel 60, 70–320 µm, Merck, Darmstadt, Germany), silica gel 60 (Kieselgel 60, 230–400 µm, Merck, Darmstadt, Germany), C-18 (Kieselgel 60 RP-18, 40–63 µm, Merck, Darmstadt, Germany), Diaion HP (Mitsubishi Chemical, Tokyo, Japan) and Sephadex LH-20 (25–100 µm, GE Healthcare, Göteborg, Sweden).
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5

Analytical Techniques for Compound Characterization

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Bruker micro TOF mass spectrometer (ESI-MS) was used for mass spectrometric analysis and a Milton Roy Spectronic 300 Array spectrophotometer was utilized for UV spectroscopic measurement. NMR spectra were obtained on a Bruker Avance III HD 500 NMR spectrometer or a Bruker Avance DPX-300 FT-NMR spectrometer. The recording of IR spectra was done by a Perkin-Elmer FT-IR 1760X spectrophotometer. Column chromatography (CC) was conducted on different stationary phases. These were silica gel 60 (Merck, Kieselgel 60, 70–320 μm), silica gel 60 (Merck, Kieselgel 60, 230–400 μm), C-18 (Merck, Kieselgel 60 RP-18, 40–63 μm) and Sephadex LH-20 (25–100 μm, GE Healthcare).
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6

Spectroscopic and Chromatographic Analysis

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UV spectra were measured by a Milton Roy Spectronic 3000 Array spectrophotometer (Rochester, Monroe, NY, USA), and IR spectra by were measured by a PerkinElmer FT-IR 1760X spectrophotometer (Boston, MA, USA). Mass spectra were obtained from a Bruker MicroTOF mass spectrometer (ESI-MS) (Billerica, MA, USA). NMR spectra were recorded on a Bruker Avance DPX-300FT NMR spectrometer or a Bruker Avance III HD 500 NMR spectrometer (Billerica, MA, USA). Microtiter plate reading was analyzed by a Biochom EZ Read 400 microplate reader (Cambridge, UK). Optical rotation was measured by a PerkinElmer Polarimeter 341 (Boston, MA, USA). Vacuum liquid column chromatography (VLC) and column chromatography (CC) were performed on silica gel 60 (Merck, Kieselgel 60, 70–320 mesh), silica gel 60 (Merck, Kieselgel 60, 230–400 mesh) (Darmstadt, Germany) and Sephadex LH-20 (25–100 μm, Pharmacia Fine Chemical Co. Ltd.) (Piscataway, NJ, USA). Yeast α-glucosidase enzyme and p-nitrophenol-α-d-glucopyranoside were purchased from Sigma Chemical, Inc. (St. Louis, MO, USA), and acarbose was obtained from Fluka Chemical (Buchs, Switzerland).
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7

Inert Atmosphere Organic Synthesis

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Materials Reactions were performed in oven-dried glassware and magnetically stirred under an inert atmosphere using a syringe tube equipped with an argon or nitrogen balloon.
Room temperature was 25°C. Commercial solvents and reagents were used as received. Anhydrous solvents were dried over 4 Å molecular sieves. All reactions were monitored by TLC using aluminium silica gel 60 F254 (Merck). IR spectra were measured on a Fourier transform (FT)-IR spectrometer, Per kinElmer, Inc. (U.S.A.) 1 H-and 13 (link) C-NMR spectra were obtained on a Bruker Avance DPX-300 FT-NMR spectrometer. 1 (link) H-NMR chemical shifts (δ) and coupling constants (J) were given in ppm and Hz, respectively. Deuterated chloroform (CDCl 3 ) served as an internal standard for both 1 H-and 13 C-NMR spectra at 7.26 and 77.0 ppm, respectively. Mass spectra were recorded on a microTOF Bruker Daltonics mass spectrometer.
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