Summary of Study ST001191
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 PR000803. The data can be accessed directly via it's Project DOI: 10.21228/M8WD6C This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST001191 |
Study Title | Metabolome of ginsenoside anti-tumor |
Study Type | Metabonomics |
Study Summary | Metabonome profiling analysis reveals the protein-metabolite interaction network of ginsenoside anti-tumor |
Institute | Nankai University |
Department | State Key Laboratory of Medicinal Chemical Biology |
Laboratory | Bai group |
Last Name | Zhihua |
First Name | Wang |
Address | 38 Tongyan Road |
15822278821@163.com | |
Phone | 02285358344 |
Submit Date | 2019-06-09 |
Raw Data Available | Yes |
Raw Data File Type(s) | wiff |
Analysis Type Detail | LC-MS |
Release Date | 2019-07-17 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR000803 |
Project DOI: | doi: 10.21228/M8WD6C |
Project Title: | Metabonome of ginsenoside |
Project Type: | Metabonomics |
Project Summary: | Metabonome profiling analysis reveals the protein-metabolite interaction network of ginsenoside anti-tumor |
Institute: | Nankai University |
Department: | State Key Laboratory of Medicinal Chemical Biology |
Laboratory: | Bai group |
Last Name: | Zhihua |
First Name: | Wang |
Address: | 38 Tongyan Road |
Email: | 15822278821@163.com |
Phone: | 02285358344 |
Subject:
Subject ID: | SU001258 |
Subject Type: | Human |
Subject Species: | Homo sapiens |
Taxonomy ID: | 9606 |
Factors:
Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)
mb_sample_id | local_sample_id | Treatment |
---|---|---|
SA082709 | NEG C-1 | Control |
SA082710 | NEG C-5 | Control |
SA082711 | NEG C-6 | Control |
SA082712 | NEG C-4 | Control |
SA082713 | NEG C-3 | Control |
SA082714 | NEG C-2 | Control |
SA082715 | NEG QC-1 | QC |
SA082716 | NEG QC-2 | QC |
SA082717 | NEG QC-3 | QC |
SA082718 | NEG S-6 | Sample |
SA082719 | NEG S-2 | Sample |
SA082720 | NEG S-1 | Sample |
SA082721 | NEG S-3 | Sample |
SA082722 | NEG S-4 | Sample |
SA082723 | NEG S-5 | Sample |
Showing results 1 to 15 of 15 |
Collection:
Collection ID: | CO001252 |
Collection Summary: | Total metabolites was extracted from the per group cell (~1x10e7) using 1 ml of methanolic acetonitrile aqueous solution (2:2:1, v/v), vortex for 60 s, hypothermia for 30 min, 2 times, place the protein for 1 h at -20 ° C, centrifuge at 14000 rcf for 20 min at 4 ° C, and freeze the supernatant. -80 ° C to save the sample |
Sample Type: | Tumor cells |
Treatment:
Treatment ID: | TR001273 |
Treatment Summary: | After cells growth in 37°C for 12 h, 0.25mg/mL ginsenosides was fed of each well and continue cultured with for 12h |
Sample Preparation:
Sampleprep ID: | SP001266 |
Sampleprep Summary: | Total metabolites was extracted from the per group cell (~1x10e7) using 1 ml of methanolic acetonitrile aqueous solution (2:2:1, v/v), vortex for 60 s, hypothermia for 30 min, 2 times, place the protein for 1 h at -20 ° C, centrifuge at 14000 rcf for 20 min at 4 ° C, and freeze the supernatant. -80 ° C to save the sample |
Combined analysis:
Analysis ID | AN001983 |
---|---|
Analysis type | MS |
Chromatography type | HILIC |
Chromatography system | Agilent 1290 |
Column | |
MS Type | ESI |
MS instrument type | Triple TOF |
MS instrument name | ABI Sciex 5600 TripleTOF |
Ion Mode | NEGATIVE |
Units | intensity |
Chromatography:
Chromatography ID: | CH001431 |
Instrument Name: | Agilent 1290 |
Column Temperature: | 25 ° C |
Flow Rate: | 0.3 mL/min |
Solvent A: | 100% water; 25 mM ammonium acetate |
Solvent B: | 100% acetonitrile |
Chromatography Type: | HILIC |
MS:
MS ID: | MS001836 |
Analysis ID: | AN001983 |
Instrument Name: | ABI Sciex 5600 TripleTOF |
Instrument Type: | Triple TOF |
MS Type: | ESI |
MS Comments: | The ESI source conditions after HILIC chromatographic separation are as follows: Ion Source Gas1 (Gas1): 60, Ion Source Gas 2 (Gas 2): 60, Curtain gas (CUR): 30, source temperature: 600 ° C, Ion Sapary Voltage Floating (ISVF) ± 5500 V (Positive and negative modes); TOF MS scan m/z range: 60-1000 Da, product ion scan m/z range: 25-1000 Da, TOF MS scan accumulation time 0.20 s/spectra, product ion scan accumulation time 0.05 s/spectra; secondary mass spectrometry is obtained using information dependent acquisition (IDA), and uses high sensitivity mode, Declustering potential (DP): ±60 V (both positive and negative modes), Collision Energy: 35±15 eV, IDA settings are as follows Exclude isotopes within 4 Da, Candidate ions to monitor per cycle: 6 |
Ion Mode: | NEGATIVE |