Sulfur content was analyzed by a Multi EA 3100 S/N Analyzer and the hydrocarbon group composition analyzed by Agilent 7890A gas chromatograph.
Elemental composition analyzed by inductively coupled plasma (ICP) method is shown as *ICP.
The polished sample was coated with carbon, and its chemical composition analyzed with an electron microprobe.
The EO content was determined and the chemical composition analyzed by GC and GC/MS.
The rate of gas evolution has been measured and the gas composition analyzed.
Body weights of an additional cohort of 18 month-old male mice (5 WT and 6 RIIβ−/−) were also measured, and their body composition analyzed in vivo using quantitative magnetic resonance (QMR) methods (Echo Medical Systems, Houston, TX).
Body composition analyzed by DXA, and BCS, BIO, BIA and US measurement are described in Table 1.
The MHC composition analyzed by SDS-PAGE showed a slightly more oxidative phenotype in HCR than in LCR rats for gastrocnemius muscle, with a similar tendency in EDL and soleus (Supplemental Table S3).
Extracellular VLP were isolated from the culture medium, and their protein composition analyzed by SDS-PAGE and Western blotting using anti-Gag and anti-HA tag antibodies: no scFvE2/p17 was detected in the VLP fraction (not shown).
Diversity estimators were utilized and wound community compositions analyzed in relation to metadata such as Age, race, gender, and comorbidities.
