Exact(3)
In order to verify the rectification method, a rectification experiment is carried out.
The rectification experiment setup is diagrammed in Additional file 1: Figure S1.
A rectification experiment of the upper and lower images in Fig. 10 was performed using the calibrated intrinsic parameters, the calculated rotation matrix, the unit translation vector, and our proposed stereo rectification method.
Similar(57)
For rectification experiments, 0.1 mM spermine was added in the intracellular solution, and 0.1 mM DL-2-amino-5-phosphonopentanoate (AP5) was present in the bath solution.
For rectification experiments, the recording chamber was perfused with ACSF containing 0.1 mM picrotoxin, 4 μM 2-chloroadenosine, and 0.1 mM d, l-aminophosphonovaleric acid (APV) at 22 25−°C.
With the same picture taken during our experiment and the rectification method proposed by Wang et al. [14], a contrast experiment can be performed under the same conditions.
This control experiment supported that the rectification was induced by functionalized dye molecules.
The control experiments supported that the observed rectification was a result of transmembrane ionic current instead of electrochemical reaction of ferricyanide.
To analyze the rectification of the Ca2+ signal propagation, additional experiments in HeLa co-cultures of HeLaCx37 and HeLaCx43 cells were performed.
Using real data captured by our system, we performed experiments with the proposed stereo calibration and rectification method and compared the data with those from some existing methods.
Here, the half-wave rectification was used as the non-linear device in our experiment with respect to EHBE method, and it provides the best performance compared with other non-linear devices according to the experimental results.
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