calcium-mediated signaling, determination of left/right symmetry, detection of nodal flow
Cellular Component (CC)
non-motile cilium
Biological Imaging Method
Spinning disk confocal microscopy, STED, AiryScan, Optical-tweezers, Spinning disk confocal microscope with custom-built optical pathway, time lapse microscopy, immunostaining, highly inclined and laminated optical sheet (HILO) microscopy, Calcium imaging, Spinning disk confocal microscopy with deconvolution, Whole-Cell FRAP (FRAPとは異なります。本論文で初めて報告した新規顕微鏡法です)
0.1001360 micrometer/slice, 1000 micrometer/slice, 0.2180928 micrometer/slice, 0.20 micrometer/pixel, NA
T scale
2 min per time interval, 1.122 sec per time interval, 0.292 sec per time interval, 100 msec per time interval, 29.12 msec per time interval, 6.550 sec per time interval, NA
Image Acquisition
Experiment type
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Microscope type
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Acquisition mode
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Contrast method
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Microscope model
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Detector model
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Objective model
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Filter set
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Related paper(s)
Contact
Takanobu A. Katoh, Toshihiro Omori, Hiroshi Hamada
, The University of Tokyo, Tohoku University, Tata Instituite for Foundamental Research
, Graduate School of Medicine, Graduate School of Biomedical Engineering, National Center for Biological Science
, Cell Biology