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Hence, supernatants of four parallel cultures were harvested on day 16.
The results are expressed as means ± standard deviations of three parallel cultures.
Standard deviation of MnP activity in parallel cultures is on average ±40 UL-1.
Parallel cultures were stimulated with CD40 or TLR agonists.
As controls and for confirmation, nuclear extracts from parallel cultures were analyzed by immunoblotting (Figure 3B).
The parallel cultures in µ-slides were prepared for CLSM analysis.
Parallel cultures were infected with JFH-1 HCVcc at an MOI of 0.01 FFU/cell.
Conversely, parallel cultures kept under normal growth medium are mostly devoid of myotubes.
Mixl1w/w and Mixl1GFP/w cells were differentiated as EBs in parallel cultures for 3d.
Parallel cultures were incubated with non-radiolabeled materials at same concentrations for calculating cell number.
Briefly, mouse splenocyte culture supernatants were harvested from parallel cultures after 48 hrs for quantification of cytokines.
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