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Compatible guard column

Manufactured by Merck Group

The Compatible Guard Column is a laboratory equipment designed to protect the analytical column by filtering out particulates and contaminants from the sample. It is placed before the analytical column to prevent premature deterioration and ensure the reliable performance of the analytical system.

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2 protocols using compatible guard column

1

Metabolite Extraction and Quantification

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The cells were subjected to metabolite extraction using our established protocol as described before.59 (link)–61 (link) The lyophilized aqueous phase metabolite samples were re-suspended in 50 % (vol/vol) acetonitrile diluted with mass-spec-grade water, while the dried organic phase metabolite samples were re-suspended in 2: 1 (vol: vol) of chloroform: methanol. Metabolomics data from the samples were acquired using a Thermo Scientific Q Exactive Orbitrap Mass Spectrometer Plus with a Vanquish UPLC system at Johns Hopkins Metabolomics Facility overseen by Dr. Anne Le. The Vanquish UPLC auto-sampler systems were used to uptake 2 μl of each sample and were maintained at 4 °C. Reverse-phase chromatography using 0.1 % formic acid in mass spec-grade water as mobile aqueous phase and 0.1 % formic acid in 98 % acetonitrile as the mobile organic phase was employed. The total runtime for each sample was 13 minutes. A Discovery® HS F5 HPLC Column with 3 μm particle size and 15 cm × 2.1 mm L × I.D. (Sigma) and a compatible guard column (Sigma) were used and were maintained at 35 °C. Data were analyzed using Thermo Fisher Scientific Compound discoverer®, Xcalibur®, and TraceFinder® softwares. The raw intensities were normalized based on protein concentration and cell weight of each sample to get the final normalized intensities.
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2

Metabolite Extraction and Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
The cells were subjected to metabolite extraction using our established protocol as described before.59 (link)–61 (link) The lyophilized aqueous phase metabolite samples were re-suspended in 50 % (vol/vol) acetonitrile diluted with mass-spec-grade water, while the dried organic phase metabolite samples were re-suspended in 2: 1 (vol: vol) of chloroform: methanol. Metabolomics data from the samples were acquired using a Thermo Scientific Q Exactive Orbitrap Mass Spectrometer Plus with a Vanquish UPLC system at Johns Hopkins Metabolomics Facility overseen by Dr. Anne Le. The Vanquish UPLC auto-sampler systems were used to uptake 2 μl of each sample and were maintained at 4 °C. Reverse-phase chromatography using 0.1 % formic acid in mass spec-grade water as mobile aqueous phase and 0.1 % formic acid in 98 % acetonitrile as the mobile organic phase was employed. The total runtime for each sample was 13 minutes. A Discovery® HS F5 HPLC Column with 3 μm particle size and 15 cm × 2.1 mm L × I.D. (Sigma) and a compatible guard column (Sigma) were used and were maintained at 35 °C. Data were analyzed using Thermo Fisher Scientific Compound discoverer®, Xcalibur®, and TraceFinder® softwares. The raw intensities were normalized based on protein concentration and cell weight of each sample to get the final normalized intensities.
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