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The PMTs were connected to a Field Programmable Gate Array (National Instruments) programmed to activate a voltage pulse when the fluorescent signal detected exceeded a gating intensity.
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A pathway that detects such falls in [Ca2+]o and indirectly activates a voltage-dependent NSCC was identified in nerve terminals in the neocortex [6].
In locust photoreceptors potassium channels are activated at a voltage close to the resting potential, around −65 mV [25], [42].
Using symmetrical 160 mM K+ solutions, the tail currents of the mSlo1 and the mSlo1+hβ2 were activated by a voltage step to −180 mV, followed by steps to potentials from –150 to 150 mV, in the presence of 10 µM Ca2+ (Fig. 1B).
Currents derived from both the wild-type mSlo and its mutant I323T (Fig. 1 B1 ) were activated by a voltage step to +160 mV, followed by steps to potentials from −180 mV to +160 mV in 10-mV increments, in symmetrical 160 mM K+ solutions with 10 μM intracellular Ca2+.
As shown above, the voltage-ramp activated a much more pronounced low-voltage outward current in WT cells than in dKO cells, with a marked shift in the 0 current potential.
This describes the single stable state (open circle) with activated (a) or inactivated (b) voltage-gated hyperpolarizing current \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$I_\mathrm{vh}$$\end{document} I vh.
STIM1 directly binds to store-operated calcium channels (SOCs), activating a highly Ca2+-selective, non-voltage-gated, inwardly rectifying current known as the Ca2+ release activated Ca2+ current (I CRAC).
Yang and colleagues 14 proposed a model in which these residues form a binding site for Mg2+, generating an electrostatic interaction with residue R288 (R213) to activate the voltage sensor.
Notably, presynaptic Eph receptors at the drosophila neuromuscular junction can activate cdc42, which in turn can activate the voltage gated calcium channel, CaV2.1.
To activate transient voltage-dependent currents, a hyperpolarizing prepulse (500 ms, −120 mV) was applied before depolarization.
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