Return to study ST003027 main page

MB Sample ID: SA328041

Local Sample ID:measured concentration(Data07-BQ-ZY20221130-600MRM-RZZ-Sample-14)
Subject ID:SU003141
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606

Select appropriate tab below to view additional metadata details:


Subject:

Subject ID:SU003141
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
measured concentration(Data07-BQ-ZY20221130-600MRM-RZZ-Sample-14)SA328041FL038939Early stage ESCCFator

Collection:

Collection ID:CO003134
Collection Summary:Tissue samples, including tumor and normal areas 5 cm away, were obtained under the guidance of experienced pathologists without compromising the patients' pathology examinations. The collected tissue was rinsed with PBS to avoid contamination, excess moisture was removed, and it was rapidly frozen in liquid nitrogen to arrest enzymatic or chemical reactions. Samples were stored at −80°C until metabolite extraction.
Collection Protocol Filename:Tissue_collection_uploaded.pdf
Sample Type:Tissue
Storage Conditions:-80℃

Treatment:

Treatment ID:TR003150
Treatment Summary:None

Sample Preparation:

Sampleprep ID:SP003147
Sampleprep Summary:For LC/MS-MS, 1000 μL of acetonitrile-methanol-H2O (2:2:1, containing isotope internal standards) was added to 50 mg samples. The samples were then homogenized, sonicated, and this process was repeated three times. After incubating the samples at -40 °C for 2 h, they were centrifuged at 12,000 rpm for 15 min at 4 °C. Subsequently, 800 μL of supernatant from each sample was transferred to a new EP tube and dried using a centrifugal concentrator. Next, 160 μL of 60% acetonitrile was added to reconstitute the dried samples. The mixture was vortexed for 30 s, and sonicated in an ice-water bath for 5 mins, followed by centrifugation at 12,000 rpm for 15 mins at 4 °C. Finally, 100 μL of supernatant from each sample was transferred into glass vials for LC-MS/MS analysis.

Combined analysis:

Analysis ID AN004962 AN004963
Analysis type MS MS
Chromatography type Normal phase Reversed phase
Chromatography system Waters Acquity H-Class Waters Acquity H-Class
Column Waters ACQUITY UPLC BEH HILIC (150 x 2.1mm,1.7um) Waters ACQUITY UPLC BEH HILIC (150 x 2.1mm,1.7um)
MS Type EI ESI
MS instrument type Triple quadrupole Triple quadrupole
MS instrument name ABI Sciex 6500 QTrap ABI Sciex 6500 QTrap
Ion Mode POSITIVE NEGATIVE
Units m/z m/z

Chromatography:

Chromatography ID:CH003745
Instrument Name:Waters Acquity H-Class
Column Name:Waters ACQUITY UPLC BEH HILIC (150 x 2.1mm,1.7um)
Column Temperature:475°C
Flow Gradient:85% (vol/vol) B: 0.0 min, 85% B to 30% B:3.0 min, 30% B to 2% B:12.0 min, 2% B:15.0 min, 2% B to 85% B: 16.0 min, 85%: 23.0 min
Flow Rate:Approximately 350–400 µl/min (back pressure should not exceed ~3,000 p.s.i. at 2% (vol/vol) B)
Solvent A:ddH2O:Acetonitrile=8:2, 10 mmol/LAmmonium acetate
Solvent B:Acetonitrile:ddH2O=9:1, 10 mmol/LAmmonium acetate
Chromatography Type:Normal phase
  
Chromatography ID:CH003746
Instrument Name:Waters Acquity H-Class
Column Name:Waters ACQUITY UPLC BEH HILIC (150 x 2.1mm,1.7um)
Column Temperature:475°C
Flow Gradient:85% (vol/vol) B: 0.0 min, 85% B to 30% B:3.0 min, 30% B to 2% B:12.0 min, 2% B:15.0 min, 2% B to 85% B: 16.0 min, 85%: 23.0 min
Flow Rate:Approximately 350–400 µl/min (back pressure should not exceed ~3,000 p.s.i. at 2% (vol/vol) B)
Solvent A:ddH2O:Acetonitrile=8:2, 10 mmol/LAmmonium acetate
Solvent B:Acetonitrile:ddH2O=9:1, 10 mmol/LAmmonium acetate
Chromatography Type:Reversed phase

MS:

MS ID:MS004702
Analysis ID:AN004962
Instrument Name:ABI Sciex 6500 QTrap
Instrument Type:Triple quadrupole
MS Type:EI
MS Comments:All the MS data acquisition and quantitative analysis of target compounds in this project were completed by SCIEX Analyst Work Station Software (1.7.2) and BIOTREE Bio Bud (2.1.4). The final concentration CF (Final Concentration, μmol/L) was directly measured by the instrument. The concentration CC (Calculated Concentration, μmol/L) multiplied by the dilute release factor page 6 / 11 Dil (Dilution Factor), in μmol/L. The target metabolite concentration CM (Metabolite Concentration, nmol/g) in the sample is equal to the final measured concentration CF times the final sample volume VF (Volume, μL) and the concentration factor CF of the sample during the pretreatment process, divided by the sample mass MS (Weight, mg), in nmol/g. NA indicated that no target metabolites were detected in the sample.
Ion Mode:POSITIVE
  
MS ID:MS004703
Analysis ID:AN004963
Instrument Name:ABI Sciex 6500 QTrap
Instrument Type:Triple quadrupole
MS Type:ESI
MS Comments:All the MS data acquisition and quantitative analysis of target compounds in this project were completed by SCIEX Analyst Work Station Software (1.7.2) and BIOTREE Bio Bud (2.1.4). The final concentration CF (Final Concentration, μmol/L) was directly measured by the instrument. The concentration CC (Calculated Concentration, μmol/L) multiplied by the dilute release factor page 6 / 11 Dil (Dilution Factor), in μmol/L. The target metabolite concentration CM (Metabolite Concentration, nmol/g) in the sample is equal to the final measured concentration CF times the final sample volume VF (Volume, μL) and the concentration factor CF of the sample during the pretreatment process, divided by the sample mass MS (Weight, mg), in nmol/g. NA indicated that no target metabolites were detected in the sample.
Ion Mode:NEGATIVE
  logo