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Abstract Using the whole-cell configuration of the patch clamp technique, calcium-activated potassium currents (IK,Ca) were investigated in ramified murine brain macrophages. In order to induce IK,Ca the intracellular concentration of nominal free Ca2+ was adjusted to 1M. The Ca2+-activated K+ current of brain macrophages did not show any voltage dependence at test potentials between 120 and +30mV...
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