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Cell membrane integrity was evaluated using a LDH release assay.
Previous studies demonstrated that the loss of membrane integrity was involved in litchi pericarp browning [1].
Plasma membrane integrity was altered in presence of VS, GNP, and GNP-VS conjugates.
Flow cytometric analysis demonstrated that S. typhimurium cell membrane integrity was destroyed following incubation with P7.
Moreover, in vitro acrosome and plasma membrane integrity was assessed and compared with AI fertility data for possible correlation.
In contrast, the amount of MDA in the roots of tetraploid rice under salt stress was significantly lower than that in diploid cultivars, suggesting that membrane integrity was higher in tetraploid cultivars than in diploid rice (Figure 4).
Cellular membrane integrity was assessed by measurement of medium LDH activity (Cytotoxicity Detection Kit, Roche, Germany).
After six hours, membrane integrity was lost and all cells had internalized HAMLET (Fig. 6A).
Cell membrane integrity was monitored at 10 minutes intervals by adding propidium iodide to the treated parasite samples (Figure 2).
Cell membrane integrity was then monitored at 10 minutes intervals by adding propidium iodide to the treated parasites.
The percent LDH release and the percent membrane integrity was calculated using the formula: (experimental release – T0 background)/(maximum release – T0 background) ×100.
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