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XB-IMG-171206

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Fig. S2. Stimulation of voltage-gated Na+ channels does not affect Ca2+ transients or Gli activity in the neural plate. (A) Two-cell-stage embryos were injected with the genetically encoded Ca2+ sensor, GCaMP6s, and time-lapse imaged at neural plate stages (stage 14, 16.25 hpf) for 30 min at 0.2 Hz in the absence or presence of 1 μM veratridine, voltage-gated Na+ channel agonist. Graph shows mean ± SEM percentage of neural plate cells exhibiting Ca2+ transients in the presence or absence of veratridine; n = 5. (B) Neural plates from embryos expressing 8GLI-luciferase were incubated for 8 h with the indicated agents and processed for luciferase activity measurements. Graph shows mean ± SEM percentage of normalized luciferase intensity compared with control (incubated with vehicle only); n = 5; *P < 0.05; ns: not significant.

Image published in: Belgacem YH and Borodinsky LN (2015)

Copyright © 2015. Image reproduced with permission of the publisher and the copyright holder. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.

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