Summary of Study ST003061

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001907. The data can be accessed directly via it's Project DOI: 10.21228/M8714X This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST003061
Study TitleUntargeted metabolomics analysis of three tea cultivars.
Study Typeleaf tissue
Study SummaryTo compare flavonoid metabolism in three tea cultivars, namely Camellia sinensis cv. "Jinfenghuang" (JFH), "Fuyun 6" (FY6) and "Bantianyao" (BTY), fresh tea leaves were plucked, rapidly ground to fine powders in liquid nitrogen and subjected to extraction by 70% methanol. The extracts were analyzed by UPLC-Quadrupole Time-of-Flight Mass Spectrometry (UPLC-QTOFMS) using an ACQUITY UPLC system in tandem to a SYNAPT G2-Si QTOF mass spectrometer (Waters, Milford, MA, USA), following the previously described method. Raw data were processed in Progenesis QI (v2.4, Nonlinear Dynamics) with default settings for peak picking and alignment. Metabolites were annotated by searching against our in-house MS/MS spectral library and public databases.
Institute
Fujian Agriculture and Forestry University
Last NameYu
First NameXiaomin
AddressShangxia Dian Road No. 15, Fuzhou 350002, Fujian, China
Emailxmyu0616@sina.com
Phone(86)18649802306
Submit Date2024-01-28
Raw Data AvailableYes
Raw Data File Type(s)raw(Waters)
Analysis Type DetailLC-MS
Release Date2024-02-05
Release Version1
Xiaomin Yu Xiaomin Yu
https://dx.doi.org/10.21228/M8714X
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Sample Preparation:

Sampleprep ID:SP003182
Sampleprep Summary:Leaves were ground into a fine powder using a pre-cooled mortar and pestle. Tea leaf powder (30 mg) was extracted with 1.0 mL of 70% methanol using ultrasonication for 20 min. After centrifugation, the supernatant was filtered through a PVDF filter (0.22 µm, Millipore).
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