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The residual leukocytes of each sample were quantified in purified erythrocytes.
Protein levels of each sample were quantified using a protein assay kit (Pierce Biotechnology, Rockford, IL).
Specific transcripts from each sample were quantified using the ABI Prism HT7900 sequence detection system (Applied Biosystems).
CCR5 and HIV-1 copies in each sample were quantified by use of the obtained threshold values from the samples and the corresponding standard curve, constructed from multiple measurements of standards.
Data from each sample were quantified relative to the housekeeping gene L32.
Protein amounts of each sample were quantified using the RC DC protein assay kit (Bio-Rad, 500 0119).
Similar(41)
The sp3 C fraction of each sample was quantified by using electron energy-loss spectroscopy (EELS).
Following DNA extraction, the mtDNA copy number in each sample was quantified by real-time polymerase chain reaction (PCR).
Samples were exposed to bacteria in solid media (nutrient agar), and the inhibition zone around each sample was quantified and put down as the antibacterial effect.
Protein in each sample was quantified using the BCA method.
Total DNA in each sample was quantified by OD260.
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