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Subtraction of the field potential from the ion-sensitive electrode voltage reading was performed.
Two electrode voltage clamp recordings of Kir2.1 and Kir2.1 T142S were done using previously described methods [9].
Two electrode voltage clamp was done as previously described.
Two electrode voltage clamp measurements in X. leavis oocytes were carried out as described previously (Brandt et al., 2012) with adjustments listed in the following.
Therefore, neglecting capacitive effects (i.e., assuming voltage to be proportional to current), the time integral of the electrode voltage can also be treated as zero.
For flow-through electrochemical reaction cells, important parameters reported are pH, electrode voltage, organic modifier content, and flow rate [ 5, 6].
Similar(51)
Two-electrode voltage clamp electrophysiology was used to functionally characterize candidate receptors expressed in Xenopus oocytes.
Briefly, two-electrode voltage clamp was performed with a TEV-200 amplifier (Dagan Corporation, Minneapolis, MN).
Constructs were expressed in Xenopus oocytes and characterized by the two-electrode voltage clamp technique.
Hemichannel currents were recorded using a two-electrode voltage clamp [63].
Standard two-electrode voltage clamp techniques were used, as previously described [82].
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