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XB-IMG-159731

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Fig. 2. Live-imaging analyses of intracellular Ca2+ in the neural plate. (A) A Ca2+ transient at the single-cell level, visualized with R-GECO1.0 (gray), in a dorsal view of the presumptive anterior spinal cord region; anterior is to the top. R-GECO1.0 was introduced on the left side of the embryo. The midline is indicated by a dotted line. A time course over a 40 s period of four sample cells (which are indicated in the figure) is shown in the right panels. Scale bar: 100 μm. (B) Time-lapse imaging data of a multicellular, wave-like Ca2+ transient in the embryo shown in A. (C) Fluorescence intensities of cytoplasmic R-GECO1.0 over time; the shaded area indicates the s.d. In multicellular Ca2+ transients (red), cells adjacent to the cell that was initially activated were measured (n=6 cells). (D) The radius and velocity of wave propagations in multicellular Ca2+ transients. The red line represents the relationship between the two data sets, calculated using the least-squares method of linear regression (n=21 cells, five embryos).

Image published in: Suzuki M et al. (2017)

Copyright © 2017. 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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