Abstract
Oocyte (egg) morphology has been shown to correlate to viability. By observing the localization of subsurface organelles we hope to learn more about oocyte structure. Mouse oocytes were collected from superovulated female C57BL/6 mice using a hormone dosing regimen. Live oocytes were then stained using multiple organellespecific fluorescent dyes and imaged on the Keck 3D Fusion Microscope (3DFM) to highlight different components of the eggs. The dyes used stained chromosomes, mitochondria, endoplasmic reticulum, membrane, tubulin, and lysosomes. Images were collected using epifluorescence and Differential Interference Contrast (DIC) microscopy and were compiled and overlaid using Metamorph software. These images serve as useful tools in exhibiting organization of developing oocytes.
Keywords
oocytes, 3DFM, differential interference contrast (DIC) microscopy
Subject Categories
Three-dimensional imaging
Disciplines
Biomedical Engineering and Bioengineering
Publisher
Bernard M. Gordon Center for Subsurface Sensing and Imaging Systems (Gordon-CenSSIS)
Publication Date
2007
Rights Holder
Bernard M. Gordon Center for Subsurface Sensing and Imaging Systems (Gordon-CenSSIS)
Permanent URL
Recommended Citation
Crooker, Robert J.; Newmark, Judith A.; and Warner, Carol M., "Mulicolor imaging of mouse oocytes" (2007). BioBED Presentations. Paper 5. http://hdl.handle.net/2047/d10009218
Click button above to open, or right-click to save.
COinS
Notes
Poster presented at the 2007 Validating TestBED and Research on Real World Problems for the I-PLUS Development Conference