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The mediators of these nongenomic responses are mERs, so it is important to understand if their levels in the membrane changed with these treatments.
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The performance of the membranes changed with a wide fluctuation of feed water temperature.
The relative proportions of diffusion and electroosmotic drag in the membrane changed significantly with the cell current of the cell.
It will be a great challenge to capture the fluid-to-soft-membrane interaction since the boundary conditions of the fluid dynamics PDE equation are more complicated since the shape of the membrane changes with time.
To investigate how the transmission properties of the photoreceptor membrane change with light adaptation, we conducted current injection experiments.
The gain function of the corresponding frequency response between the current input and the voltage output is the complex impedance, Z [43]. Figure 11C shows how filtering properties (low-pass features of the impedance function) of the membrane change with light BGs at 19°C.
Meanwhile, the membranes were responded to both anion species (including PF6−, BF4− and SCN-) and their strength: the pure water fluxes and the morphologies of the modified membranes changed associated with different types of anions, and the membranes after ion-exchanging also showed obvious anion strength responsive behaviors to the corresponding salt solutions.
ATPase that was used to verify the purity of the membrane fraction also changed with E-cadherin expression.
We also investigate how their membrane properties change with these conditions by injecting current waveforms intracellularly.
The housekeeping gene of B. japonicum, sigA, was used as an internal reference for quantitative real-time RT PCR as reported previously, since the expression levels of sigA gene, which was regularly spotted on the array membranes, were not significantly changed with the SSE/genistein-treatment in this experimental condition.
Using live cancer cells without fixation, plasma membrane changes associated with apoptosis have been detected with Annexin V-FITC/PI bindings that represent apoptotic exploration and by monitoring the location of phosphatidylserine (PS) and integrity/permeability of cell membranes after treatment [ 5].
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