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For each extract a phytochemical screening was performed.
Each extract was treated to U266B1 cells and primary B cells to compare their inhibitory effects on IgE secretion.
For each extract, three measurements were performed.
The NO-scavenging activity of each extract was also measured.
We conducted at least 3 replicates for each extract.
Destruction of each extract ranged between 1.5 2.9%. of each extract.
50 µg each extract was resolved by 10% SDS-PAGE.
SF2/ASF was immunoprecipitated from each extract under stringent conditions.
Two MS signatures (in the positive and negative modes) were obtained from each extract fraction.
The CT values were recorded as proxies for the relative DNA preservation in each extract.
The apoptotic potency of each extract was assayed at 0, 2 and 4 hours.
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