Data files
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This file contains the processed LC–MS/MS results for intracellular metabolite quantification using the isotope-ratio approach. It provides the C12/C13 ratios for all metabolites in each sample, calculated relative to the 13C-labelled internal standard. The dataset also includes the retention times and the measurement quality scores for each metabolite, enabling assessment of peak identification and data reliability. The raw LC–MS/MS data used to generate these results are available from the ...
Creator: Janette Alford
Submitter: Janette Alford
This file contains the data generated for extracellular metabolite quantification using HPLC–MS. It includes the extracted ion chromatograms (EICs) and total ion chromatograms (TICs) for all measured metabolites within the samples and within the calibration standards, as well as the peak heights obtained for both the calibration standards and the extracellular samples. These data support the calculation of metabolite concentrations based on calibration curves.
Creator: Janette Alford
Submitter: Janette Alford
This file contains metadata associated with the metabolomics sampling procedure. It includes (i) optical density (OD) measurements of each culture at the time of sampling for intracellular and extracellular metabolite quantification, and (ii) the sample label table used for intracellular metabolite analysis. The table provides, for each sample, the sample label/number, collected sample volume, quenching volume, and the mapping to the corresponding biological sample.
Creator: Janette Alford
Submitter: Janette Alford
This file contains the data generated for glycogen quantification. It includes the raw absorbance measurements at 540 nm for each sample, the corresponding culture optical densities (OD) at the time of sampling, and the calibration curve data (absorbance values and associated glucose standards) used to calculate glucose concentrations from the measured absorbance values.
Creator: Janette Alford
Submitter: Janette Alford
Biochemical Reaction Networks Biochemical Reaction Networks transform static protein-protein interactions (PPI) network into dynamic, mechanistic models by decomposing each interaction into underlying molecular events like phosphorylation and complex formation. Using SPADAN toolbox (DOI:10.1093/bioinformatics/btad079), we expands PPI network into biochemical reactions network.
Ordinary Differential Equation Model Equations Kinetic descriptions of biochemical reactions related to each renal cell ...
Creator: Farnoush Kiyanpour
Submitter: Farnoush Kiyanpour
Immunoblotting gel images, annotations, results
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
Batch sample publishing
Creator: Charles Demurjian
Submitter: Charles Demurjian
For more than a thousand chemical species of biological interest the table gives standard chemical, standard apparent chemical, and dtandard metabolic potentials:
- Standard chemical potentials: extracted from various literature references (data sources indicated below the Table)
- Standard apparent chemical potentials as the above standard chemical potentials but further transformed for H+ and ionic strength; for Alberty conditions (pH=7.14, pMg=3.57, I=0.25 M Osm=0 M) and for new biochemical ...
Creator: Hans V. Westerhoff
Submitter: Hans V. Westerhoff
L. infantum promastigotes were administered with EC10 and EC50 concentrations of H80 and Miltefosine. Cells were fractionated into soluble (cyto), insoluble (membranes), and mitochondiral lysates, and analysed through LC-MS/MS Proteomics.
Creators: Giulia Malpezzi, Lorenzo Tagliazucchi, Maria Paola Costi
Submitter: Giulia Malpezzi
Analysis to determine fold change in mRNA for selected targets (COX-2, IL1B, IL8, 5-LOX, TLR4, iNOS, TNFa)
Illustration of bovine lung explant (BLE) in Tissue Culture Medium (TCM).
Analysis to determine fold change in mRNA for selected targets (COX-2, IL1B, IL8, 5-LOX, TLR4, iNOS, TNFa)
Creator: Leruo Keokilwe
Submitter: Leruo Keokilwe
Creator: Charles Demurjian
Submitter: Charles Demurjian
Creator: Charles Demurjian
Submitter: Charles Demurjian
Creator: Charles Demurjian
Submitter: Charles Demurjian
Creator: Inken Wohlers
Submitter: Inken Wohlers
Creator: Inken Wohlers
Submitter: Inken Wohlers
Creator: Inken Wohlers
Submitter: Inken Wohlers
Creator: Inken Wohlers
Submitter: Inken Wohlers
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