Summary of Study ST001120

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 PR000751. The data can be accessed directly via it's Project DOI: 10.21228/M8M676 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.

Show all samples  |  Perform analysis on untargeted data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files
Study IDST001120
Study TitleReprogrammed Lipid Metabolism in Bladder Cancer with Cisplatin Resistance
Study SummaryThis study conducted comprehensive and comparative lipidomic profiling of two isogenic human T24 bladder cell lines, which are characterized as sensitive or resistant to the cisplatin-induced cell apoptosis.
Institute
Cedars-Sinai Medical Center
DepartmentDepartments of Surgery and Biomedical Sciences
Last NameKim
First NameJayoung
Address8700 Beverly Blvd., Davis 5071 Los Angeles, CA 90048, USA
EmailJayoung.Kim@cshs.org
Phone310-423-7168
Submit Date2017-04-10
Study CommentsTreatment with ACSS1 inhibitor
Analysis Type DetailLC-MS
Release Date2019-03-06
Release Version1
Jayoung Kim Jayoung Kim
https://dx.doi.org/10.21228/M8M676
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Collection:

Collection ID:CO001171
Collection Summary:T24 BC cells were obtained and cultured, according to instructions provided by the ATCC. Media was supplemented with 10% fetal bovine serum, 2% glutamine and 1% antibiotics (Invitrogen, Carlsbad, CA). Cells were maintained under a humidified atmosphere of 5% CO2 at 37°C. These cell lines were negative for mycoplasma and all other infectious agents evaluated.
Sample Type:Cultured cells
  logo