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MB Sample ID: SA243491

Local Sample ID:chdwb-urine009
Subject ID:SU002525
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Age Or Age Range:40-69
Weight Or Weight Range:100-350 lbs
Height Or Height Range:58-78 inches
Gender:Male and female

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Subject:

Subject ID:SU002525
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Age Or Age Range:40-69
Weight Or Weight Range:100-350 lbs
Height Or Height Range:58-78 inches
Gender:Male and female

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
chdwb-urine009SA243491FL0305047.257308358S-S PyC2-Gly (uM)

Collection:

Collection ID:CO002518
Collection Summary:Samples were collected using standard operating procedures in the Center for Health Discovery and Well Being (CHDWB) cohort of healthy adults. The CHDWB enrolled 763 participants starting in 2008 with approval from the Emory Institutional Review Board (IRB approval No. 00007243). The original study included both genders and included individuals self-identifying as white, black, Hispanic and Asian. The present study selected available archival samples from 143 individuals without known disease. Urine samples included one sample per individual that was collected at either baseline, 6 months, or 12 months. Urine samples were stored at -80 ºC prior to analysis
Sample Type:Urine

Treatment:

Treatment ID:TR002537
Treatment Summary:This study used archival samples from an observational study. No treatment was performed.

Sample Preparation:

Sampleprep ID:SP002531
Sampleprep Summary:Samples were prepared following the Emory University Clinical Biomarkers Laboratory SOP for high resolution metabolomics sample preparation. Urine was thawed from -80 °C on ice and vortexed to homogenize. 50 μL urine was transferred to a clean microcentrifuge tube and treated with with 100 μL LC-MS grade acetonitrile containing 2.5 μL internal standard solution. Urine was equilibrated on ice for 30 min. Precipitated proteins were removed by centrifuge (16100 x g at 4 °C for 10 min). 100 μL supernatant was removed and added to an autosampler vial. Samples were maintained at 4 °C until analysis. Samples were prepared alongside NIST SRM 1950 and q3June2014 reference standards.
Sampleprep Protocol Filename:EmoryUniversity_HRM_QEHF-MassSpec_092017_v1.pdf

Combined analysis:

Analysis ID AN003969
Analysis type MS
Chromatography type HILIC
Chromatography system Thermo Dionex Ultimate 3000
Column Waters XBridge BEH Amide (50 x 2.1mm,2.5um)
MS Type ESI
MS instrument type Orbitrap
MS instrument name Thermo Q Exactive HF hybrid Orbitrap
Ion Mode POSITIVE
Units Peak area

Chromatography:

Chromatography ID:CH002935
Methods Filename:EmoryUniversity_HRM-QEHF_chromatography_5min_092017_v1.pdf
Instrument Name:Thermo Dionex Ultimate 3000
Column Name:Waters XBridge BEH Amide (50 x 2.1mm,2.5um)
Column Temperature:60
Flow Gradient:A= water, B= acetontrile, C= 2% formic acid in water; 22.5% A, 75% B, 2.5% C hold for 1.5 min, linear gradient to 77.5% A, 20% B, 2.5% C at 4 min, hold for 1 min
Flow Rate:0.35 mL/min for 1.5 min; linear increase to 0.4 mL/min at 4 min, hold for 1 min
Solvent A:100% water
Solvent B:100% acetonitrile
Chromatography Type:HILIC

MS:

MS ID:MS003703
Analysis ID:AN003969
Instrument Name:Thermo Q Exactive HF hybrid Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:Raw analysis files from urine analyses were converted to .mzXML using ProteoWizard v3. Data extraction was performed using apLCMS v6.3.3 and xMSanalyzer v2.0.8, generating m/z features consisting of an m/z, retention time (RT) and ion intensity. Feature and sample filtering retained features with a median CV of 50% or less, with a minimum mean Pearson correlation coefficient of 0.7 between technical replicates, and which were detected in at least 30% of samples. Technical replicates were median summarized.
Ion Mode:POSITIVE
Analysis Protocol File:EmoryUniversity_HRM_QEHF-MassSpec_092017_v1.pdf
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