Return to study ST000261 main page

MB Sample ID: SA012005

Local Sample ID:P341
Subject ID:SU000281
Subject Type:Animal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:C57BL/6J
Species Group:Mammal

Select appropriate tab below to view additional metadata details:


Subject:

Subject ID:SU000281
Subject Type:Animal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:C57BL/6J
Species Group:Mammal

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
P341SA012005FL0029431Disease? (0, no; 1, yes)
P341SA012005FL0029433Dosage (Gy)

Collection:

Collection ID:CO000275
Collection Summary:Spleens were dissected and snap-frozen at -80°C before NMR spectroscopy and morphology analysis.
Sample Type:Tissue

Treatment:

Treatment ID:TR000295
Treatment Summary:A total of 17 seven-week-old C57BL/6 female mice were randomly grouped before total body being exposed to gamma irradiation using a high activity gamma source (1250 keV 60Co). The linear energy transfer (LET) associated with these fields is in the range of 0.2-2 keV/?m. For the total body gamma radiation, the animals were isolated to the corner of their polymer cages, placed at a minimum of 100 cm from the collimated 6000 Ci 60Co source, and then irradiated to the proposed dosage. The resulting absorbed dose rate at approximately 600 mg/cm2 depth was 0.83Gy/min relative to tissue. Groups of mice were exposed to radiation doses of 0Gy (control, n=8), 3.0Gy (n=5) and 7.8Gy (n=4). After 4 days post exposure, mice were sacrificed with 70/30 CO2/O2 .

Sample Preparation:

Sampleprep ID:SP000289
Sampleprep Summary:Cold Methanol/H2O/Chloroform Extraction
Sampleprep Protocol Comments:Extraction protocol: Step 1: Weight each intact frozen tissue and add 0.25 ml methanol and 0.053 ml deionized water for each sample, after homogenizing in ice bath using the Tissue Tearor (Model 985-370, BioSpec Products, Inc.), then following by vortexing the mixture and then adding 0.125 ml chloroform, vortexing again. Step 2: 0.125 ml chloroform and 0.125 ml deionized water were added to the sample and then vortexed again, following by transferring different layers into glass vials separately with syringes after the mixture being left on ice for 15 min and centrifuged at 6,000 rpm for 16 min at 4 °C. Finally, the MeOH/H2O layer solvents (hydrophilic metabolites) were removed by employing the lyophilizer. And the extracts were stored at ?80 °C freezer before performing NMR measurements.

Analysis:

MB Sample ID:SA012005
Analysis ID:AN000416
Analysis Type:NMR
Software Version:Vnmrj/ 4.0; Chenomx/8.1
Chromatography ID:CH000293
Num Factors:3

NMR:

NMR ID:NM000058
Analysis ID:AN000416
Instrument Name:Varian 600 MHz
Instrument Type:FT-NMR
NMR Experiment Type:1D
Spectrometer Frequency:600 MHZ
Power Level:Deuterium
Receiver Gain:0.05 mM
Presaturation Power Level:5mm HCN probe with Z axis-gradient
Chemical Shift Ref Cpd:D2O
Temperature:5mm * 8 in
Number Of Scans:Gradient shim
Dummy Scans:PRESAT
Acquisition Time:presat
Relaxation Delay:7.5 us
Zero Filling:DSS
Apodization:293 K
Baseline Correction Method:19968
  logo