Return to study ST001329 main page

MB Sample ID: SA096450

Local Sample ID:JW44-NP
Subject ID:SU001403
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:C57BL/6
Age Or Age Range:5-6 months or 26 months
Animal Animal Supplier:NIA
Animal Housing:UW ARCF
Animal Feed:Ad libitum
Animal Water:Ad libitum

Select appropriate tab below to view additional metadata details:


Subject:

Subject ID:SU001403
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:C57BL/6
Age Or Age Range:5-6 months or 26 months
Animal Animal Supplier:NIA
Animal Housing:UW ARCF
Animal Feed:Ad libitum
Animal Water:Ad libitum

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
JW44-NPSA096450FL01360226Age (Months)
JW44-NPSA096450FL013602SS-31 (3 mg/kg/day) + NMN (300 mg/kg/day)Treatment

Collection:

Collection ID:CO001398
Collection Summary:Hearts were removed from mice immediately following live cervical dislocation euthanasia. Hearts were flushed with sterile normal saline, cut into large chunks, and snap frozen in liquid nitrogen.
Sample Type:Heart

Treatment:

Treatment ID:TR001418
Treatment Summary:Mice were treated with SS-31, NMN, neither, or both for 8 weeks. SS-31 was administered through subdermal osmotic pumps at a 3 mg/kg body weight/day dose. NMN was administered through drinking water at a 300 mg/kg body weight/day dose.
Treatment Compound:SS-31 and NMN
Treatment Route:Subdermal osmotic pump for SS-31, drinking water for NMN
Treatment Dose:3 mg/kg body weight/day for SS-31, 300 mg/kg body weight/day for NMN

Sample Preparation:

Sampleprep ID:SP001411
Sampleprep Summary:Heart tissue samples were homogenized in water and methanol with spiked stable isotopes as internal QC standards. Samples were purified by pelleting proteins, drying of the solution via Speedvac (Thermo Fisher Scientific), and reconstituting in HILIC solvent.

Combined analysis:

Analysis ID AN002215
Analysis type MS
Chromatography type HILIC
Chromatography system Shimadzu Nexera XR LC-20AD
Column Waters Acquity BEH Amide (150 x 2.1mm,1.7um)
MS Type ESI
MS instrument type Triple quadrupole
MS instrument name ABI Sciex 6500 QTrap
Ion Mode UNSPECIFIED
Units Peak Area

Chromatography:

Chromatography ID:CH001625
Chromatography Summary:Samples were injected into a chromatography system consisting of a dual injection valve setup allowing injections onto two different LC columns with each column dedicated to an ESI polarity. 5 µL were injected on the positive mode column and 10 µL on the negative side column. The columns were a matched pair from the same production lot number and were both a Waters XBridge BEH amide column (2.1 x 150 mm). Autosampler was maintained at 4 °C and column oven was set to 40 °C. 0.3 mL/min gradient was 0-3 min 95% B, 3-8 min 95 -> 50% B, 8-12 min 50% B, 12-13 min 50 – 95% B, 13-18 min 95% B. After completion of the 18 minute gradient, injection on the opposite column was initiated and the inactive column was allowed to equilibrate at starting gradient conditions. A set of QC injections for both instrument and sample QC were run at the beginning and end of the sample run.
Instrument Name:Shimadzu Nexera XR LC-20AD
Column Name:Waters Acquity BEH Amide (150 x 2.1mm,1.7um)
Column Temperature:40
Solvent A:95% water/3% acetonitrile/2% methanol; 0.2% acetic acid; 10 mM ammonium acetate
Solvent B:93% acetonitrile/5% water/2% methanol; 0.2% acetic acid; 10 mM ammonium acetate
Chromatography Type:HILIC

MS:

MS ID:MS002061
Analysis ID:AN002215
Instrument Name:ABI Sciex 6500 QTrap
Instrument Type:Triple quadrupole
MS Type:ESI
MS Comments:Samples were injected into a chromatography system consisting of a dual injection valve setup allowing injections onto two different LC columns with each column dedicated to an ESI polarity. 5 µL were injected on the positive mode column and 10 µL on the negative side column. The columns were a matched pair from the same production lot number and were both a Waters XBridge BEH amide column (2.1 x 150 mm). Autosampler was maintained at 4 °C and column oven was set to 40 °C. 0.3 mL/min gradient was 0-3 min 95% B, 3-8 min 95 -> 50% B, 8-12 min 50% B, 12-13 min 50 – 95% B, 13-18 min 95% B. After completion of the 18 minute gradient, injection on the opposite column was initiated and the inactive column was allowed to equilibrate at starting gradient conditions. A set of QC injections for both instrument and sample QC were run at the beginning and end of the sample run. Data was integrated by MultiQuant 3.0.2 or Sciex-OS v1.5 software. Peaks were selected based on peak shape, a signal-to-noise of 10 or better and retention times consistent with previously run standards and sample sets.
Ion Mode:UNSPECIFIED
  logo