Summary of Study ST000261

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 PR000212. The data can be accessed directly via it's Project DOI: 10.21228/M80C7B This work is supported by NIH grant, U2C- DK119886.

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

Perform statistical analysis  |  Show all samples  |  Download binned data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST000261
Study Title1H NMR metabolomics study of spleen from C57BL/6 mice exposed to gamma radiation
Study TypeTissue Extracts Comparison
Study SummaryTissue extracts from exposure to gamma radiation mouse spleen and controls were compared via NMR based metabolomic analysis
Institute
Pacific Northwest National Laboratory
DepartmentFundamental & Computational Sciences
Last NameHu
First NameJianzhi
Address--
Emailjianzhi.hu@pnnl.gov
Phone--
Submit Date2015-10-26
Raw Data AvailableYes
Raw Data File Type(s)fid
Uploaded File Size24M
Analysis Type DetailNMR
Release Date2015-10-26
Release Version1
Jianzhi Hu Jianzhi Hu
https://dx.doi.org/10.21228/M80C7B
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Sample Preparation:

Sampleprep ID:SP000289
Sampleprep Summary:Cold Methanol/H2O/Chloroform Extraction
Sampleprep Protocol Comments:Extraction protocol: Step 1: Weight each intact frozen tissue and add 0.25 ml methanol and 0.053 ml deionized water for each sample, after homogenizing in ice bath using the Tissue Tearor (Model 985-370, BioSpec Products, Inc.), then following by vortexing the mixture and then adding 0.125 ml chloroform, vortexing again. Step 2: 0.125 ml chloroform and 0.125 ml deionized water were added to the sample and then vortexed again, following by transferring different layers into glass vials separately with syringes after the mixture being left on ice for 15 min and centrifuged at 6,000 rpm for 16 min at 4 °C. Finally, the MeOH/H2O layer solvents (hydrophilic metabolites) were removed by employing the lyophilizer. And the extracts were stored at ?80 °C freezer before performing NMR measurements.
  logo