Add time:07/16/2019         Source:sciencedirect.com

The low-affinity Ca2+ indicator Mag-Indo-1 was used to measure increments of ionised Ca2+ concentration in the cytoplasm of single smooth muscle cells isolated from guinea-pig urinary bladder. With 3.6 mM [Ca2+]0, depolarization steps to 0 mV were associated with a transient increase of fluorescence ratio (F410/F470) only when ICa triggered a Ca2+-induced Ca2+ release (CICR). [Ca2+]i transiently peaked to 3–5 μM and despite continuous Ca2+ influx the [Ca2+]i signal fell close to the baseline. Rapidly applied caffeine (10 mM) increased [Ca2+]i by 16 μM, the response was completely blocked by intracellular ryanodine (20 μM). With ryanodine intracellularly, ICa produced very small [Ca2+]i signals unless it was augmented by elevation of [Ca2+]0 to 10 mM and addition of 1 μM Bay K8644. Under these conditions, [Ca2+]i responded with a tonic elevation lasting as long as the depolarizing pulse. It is concluded that the low-affinity indicator Mag-Indo-1 reports predominantly Ca2+ release from SR in cytoplasm.

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