MassIVE MSV000086870

Partial Public

GNPS Colostethus imbricolus - SBC18 column

Description

All analysis were performed in reversed-phase HPLC Zorbax SB-C18 column (150 mm x 2.0 mm x 3.0 um, Agilent technologies, Santa Clara, USA) for optimizing the separation conditions. The mobile phases were A (0.1% v/v formic acid in Milli-Q water) and B (0.1% v/v formic acid in ACN) at a flow rate of 0.3 mL/min and 45ºC. Gradient elution started to 5%B for 2 min, then increased to 20%B at 4 min, then to 30%B at 15 min, 34%B at 25 min, 45%B at 30, and finally to 100%B at 45 min and maintained for 5 min and thereafter returned back to starting conditions in 2 min and finally 13 min of re-equilibration time was applied. Total run time was 65 min. MS spectra were acquired in positive ion mode in the range of 20–2000 m/z and a scan rate of 6 scan/min. 10 uL of each frog extract was injected by duplicate using an the same HPLC-Q-TOF system (Agilent Technologies, Santa Clara, CA, USA) employed for the targeted analysis. Mass range for the full scan was performed between 20 to 2000 m/z, nebulizer gas flow rate of 8 L/min, pressure of 10 psi, and fragmentor of 175 V. The mass correction was performed on the same way that for the targeted analysis. For MS/MS analysis, auto MS/MS acquisition mode was employed for the analysis of one of the samples employing a mass range between 100 to 3000 m/z, a scan rate of 6.0 scans/s, isolation width of 1.3 amu, [doi:10.25345/C5SZ22] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Poison frogs ; Dendrobatoidea ; TTX ; Alkaloids

Contact

Principal Investigators:
(in alphabetical order)
Mabel Gonzalez, Uniandes, Colombia
Submitting User: mabel_gonzalez
Number of Files:
Total Size:
Spectra:
Subscribers:
 
Owner Reanalyses
Experimental Design
    Conditions:
    Biological Replicates:
    Technical Replicates:
 
Identification Results
    Proteins (Human, Remapped):
    Proteins (Reported):
    Peptides:
    Variant Peptides:
    PSMs:
 
Quantification Results
    Differential Proteins:
    Quantified Proteins:
 
Browse Dataset Files
 
FTP Download Link (click to copy):

- Dataset Reanalyses


+ Dataset History


GNPS content goes here (MSV000086870 [task=c2782defa98d4b37a43565b1af7a269b])
Click here to queue conversion of this dataset's submitted spectrum files to open formats (e.g. mzML). This process may take some time.

When complete, the converted files will be available in the "ccms_peak" subdirectory of the dataset's FTP space (accessible via the "FTP Download" link to the right).
Number of distinct conditions across all analyses (original submission and reanalyses) associated with this dataset.

Distinct condition labels are counted across all files submitted in the "Metadata" category having a "Condition" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct biological replicates across all analyses (original submission and reanalyses) associated with this dataset.

Distinct replicate labels are counted across all files submitted in the "Metadata" category having a "BioReplicate" or "Replicate" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct technical replicates across all analyses (original submission and reanalyses) associated with this dataset.

The technical replicate count is defined as the maximum number of times any one distinct combination of condition and biological replicate was analyzed across all files submitted in the "Metadata" category. In the case of fractionated experiments, only the first fraction is considered.

"N/A" means no results of this type were submitted.
Originally identified proteins that were automatically remapped by MassIVE to proteins in the SwissProt human reference database.

"N/A" means no results of this type were submitted.
Number of distinct protein accessions reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct unmodified peptide sequences reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct peptide sequences (including modified variants or peptidoforms) reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Total number of peptide-spectrum matches (i.e. spectrum identifications) reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct proteins quantified across all analyses (original submission and reanalyses) associated with this dataset.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct proteins found to be differentially abundant in at least one comparison across all analyses (original submission and reanalyses) associated with this dataset.

A protein is differentially abundant if its change in abundance across conditions is found to be statistically significant with an adjusted p-value <= 0.05 and lists no issues associated with statistical tests for differential abundance.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
This dataset may not contain all raw spectra data as originally deposited in PRIDE. It has been imported to MassIVE for reanalysis purposes, so its spectra data here may consist solely of processed peak lists suitable for reanalysis with most software.