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*CIL – Cell Image Library accession number. Please use this to reference an image.

CIL:12820*  Cite 
Description

Calcium and Cleavage Furrows, animal pole view. Fertilized zebrafish eggs were collected within 5 min of spawning, enzymatically dechorionated, and injected with approximately 0.9 nl of a 1% solution of recombinant f-aequorin in 100 mM KCl, 5 mM Mops, and 50 μM EDTA. During imaging the embryos were maintained at 28°C in 30% Danieau's medium containing penicillin (0.5 mg/ml), streptomycin (5,000 units/ml; Sigma), and 0.5% methylcellulose. Imaging was performed on a Photon Imaging Microscope (Science Wares, Falmouth, MA) that used a photon-counting spatial detector with a resistive anode output (Photek, St. Albens-on-Sea, U.K.). Digitized detector output in the form of a stream of time-labeled eight-bit x--y coordinates (256 × 256 pixels) was used to construct time-lapse imaging sequences. The imaging system software allowed the original photon data stream to be analyzed according to any chosen integration time, with the resulting image frames maintaining accurate photon quantitation up to 256 photons per pixel.These images are part of an image series within the Zebrafish--The Living Laboratory CD made available by Mark Cooper and described in Methods in Cell Biology Volume 77, 2004, Pages 439-457.

Biological Sources
NCBI Organism Classification
Danio rerio
Cell Line
Embryo
Cellular Component
cleavage furrow
Biological Context
Biological Process
detection of calcium ion
Attribution
Names
Andy Miller
Sarah Webb
Published
PNAS January 5, 1999 vol. 96: 157-161
Pubmed
9874788
OTHER
Hong Kong University of Science and Technology, Hong Kong, China
Zebrafish -- The Living Laboratory
Methods in Cell Biology Volume 77, 2004, Pages 439-457
Citation
Digital Object Identifier (DOI)
doi:10.7295/W9CIL12820
Archival Resource Key (ARK)
ark:/b7295/w9cil12820
Grouping This image is part of a group.
Imaging
Image Type
recorded image
Image Mode
fluorescence microscopy
bright-field microscopy
Parameters Imaged
bioluminescence
absorption of illumination
Source of Contrast
distribution of a specific protein
differences in intrinsic optical density
Visualization Methods
f-aequorin
Processing History
color coded photon count
Data Qualifiers
processed data
Sample Preparation
Methods
living tissue
microinject
Relation To Intact Cell
whole mounted tissue
Dimensions
Spatial Axis Image Size Pixel Size
X —— 2.5µm
Y —— 2.5µm