Summary of Study ST003101

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 PR001924. The data can be accessed directly via it's Project DOI: 10.21228/M81B11 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.

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Study IDST003101
Study TitleParallel pheromonal, metabolite, and lipid analyses reveal patterns associated with early life transitions and ovary activation in honey bee (Apis mellifera) queens
Study SummaryWe used a novel pheromone detection method to quantify retinue pheromone (QRP) concurrently with shotgun metabolomics and lipidomics analysis to determine what changes in pheromones and small molecules may underpin differences in age, laying status, and acceptance by workers in honey bee queens.
Institute
Life Sciences Institute, The University of British Columbia
Last NameAlcazar Magana
First NameArmando
Address2350 Health Sciences Mall, Vancouver, BC, V6T1Z3, Canada
Emailarmando.alcazarmagana@ubc.ca
Phone5416097172
Submit Date2024-02-20
Num Groups4
Total Subjects40
Num Females40
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2024-05-24
Release Version1
Armando Alcazar Magana Armando Alcazar Magana
https://dx.doi.org/10.21228/M81B11
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Combined analysis:

Analysis ID AN005072 AN005073 AN005074 AN005075
Analysis type MS MS MS MS
Chromatography type Reversed phase Reversed phase Reversed phase Reversed phase
Chromatography system Thermo Vanquish Thermo Vanquish Thermo Vanquish Thermo Vanquish
Column Inertsil Ph-3 UHPLC column (2 µm, 150 x 2.1 mm) Inertsil Ph-3 UHPLC column (2 µm, 150 x 2.1 mm) Waters ACQUITY UPLC CSH C18 (100 x 2.1mm,1.7um) Waters ACQUITY UPLC CSH C18 (100 x 2.1mm,1.7um)
MS Type ESI ESI ESI ESI
MS instrument type QTOF QTOF QTOF QTOF
MS instrument name Bruker Impact II Bruker Impact II Bruker Impact II Bruker Impact II
Ion Mode POSITIVE NEGATIVE POSITIVE NEGATIVE
Units Rel Abundance Rel Abundance Rel Abundance Rel Abundance

MS:

MS ID:MS004810
Analysis ID:AN005072
Instrument Name:Bruker Impact II
Instrument Type:QTOF
MS Type:ESI
MS Comments:For positive ion mode, the mass spectrometer settings were as follows: capillary voltage of 4500 V, nebulizer gas pressure of 2.0 bar, dry gas flow rate of 9 L min-1, dry gas temperature of 220°C, mass scan range of 60-1300 m/z, and a total cycle time of 0.6 s. To obtain comprehensive structural information, collision energy of 20 V was ramped through each MS/MS scan from 100 to 250%.
Ion Mode:POSITIVE
  
MS ID:MS004811
Analysis ID:AN005073
Instrument Name:Bruker Impact II
Instrument Type:QTOF
MS Type:ESI
MS Comments:For negative ionization mode, the capillary voltage was set at -3500 V.
Ion Mode:NEGATIVE
  
MS ID:MS004812
Analysis ID:AN005074
Instrument Name:Bruker Impact II
Instrument Type:QTOF
MS Type:ESI
MS Comments:Data was collected using data-dependent high-resolution mass spectral acquisition (LC-HRMS/MS - Bruker Impact II) in ESI+ and ESI-. For ESI+, the mass spectrometer settings were as follows: capillary voltage of 4500 V, nebulizer gas pressure of 2.0 bar, dry gas flow rate of 9 L min-1, dry gas temperature of 220°C, mass scan range of 100-1700 m/z. To achieve a lower limits of detection, spectra acquisition rate was set at 3 Hz, and a cycle time of 0.6 s. Collision energy of 20 V was ramped through each MS/MS scan from 100 to 250%
Ion Mode:POSITIVE
  
MS ID:MS004813
Analysis ID:AN005075
Instrument Name:Bruker Impact II
Instrument Type:QTOF
MS Type:ESI
MS Comments:For ESI-, the capillary voltage was set at -3800 V.
Ion Mode:NEGATIVE
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