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Each Egyptian serum sample was analyzed in triplicate in a particular assay.
The accuracy of this new method proved superior to that of bromocresol when an international standard serum sample was analyzed.
In HUNT 2, a nonfasting venous serum sample was analyzed for glucose; for those who reported diabetes, an EDTA whole-blood sample was also analyzed for A1C.
We purchased a pooled human serum sample from Intergen (Milford, MA, USA); this serum sample was analyzed by graphite-furnace atomic absorption spectroscopy (AAS) and shown to be free of endogenous cadmium (data not shown).
An aliquot of the serum sample was analyzed using the above analytical HPLC system to determine the percentage of intact F-ML-8 in 30, 60, 90, and 120 min.
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The clustering of Raman spectra of serum sample is analyzed using the super-paramagnetic clustering technique based in the Potts spin model.
Multiple aliquots of a control pooled serum sample were analyzed (intra-assay CV < 3.0%).
Multiple aliquots of a control pooled serum sample were analyzed during each batch of analyses (intra-assay CV < 4.5%).
The distribution of adiponectin multimers in serum samples was analyzed under nonreducing and nondenaturing conditions [ 11].
The levels of the enzymes in serum samples were analyzed by an automatic biochemistry analyzer TBA-2000FRR, Tokyo, Japanyo, Japan).
The serum samples were analyzed using Dimension Expanded Auto-analyzer to determine serum sodium (Na+), potassium (k+) and calcium (Ca++) levels.
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