CIL:35431, Mus musculus, oocyte. CIL. Dataset

NCBI Organism:Mus musculus; Cell Types:oocyte Cell Components:microtubule, microtubule organizing center part, nuclear chromosome; Biological process:meiotic spindle organization, microtubule organizing center organization;

Licensing

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

CIL:35431^* Cite

Description

This 3 panel image displays meiosis in a mouse oocyte triple labelled for microtubules (panel 1 and green), phosphorylated-Transforming Acidic Coiled-Coil protein (TACC3; panel 2 and red), and nucleic acids (blue). This oocyte was injected with siTPX2-5h, a doublestranded siRNA against TPX2 (targeting protein for Xenopus kinesin-like protein, xklp2)and rescued with the coinjection of YFP-TPX2. Figure 7a, third row. doi:10.1371/journal.pone.0003338.g007

Technical Details

Time-lapse images were acquired using a Photometrics CCD camera (CoolSnap HQ2) mounted on a Leica DMI600B microscope using a Leica HC PL APO 20X/0.7 NA objective enclosed in a thermostatic chamber (Life Imaging Services). Immunofluorescence methods can be found in the cited paper and in Brunet S. et al. (1999) J Cell Biol 146: 1–11.

Biological Sources

NCBI Organism Classification: Mus musculus
Cell Type: oocyte
Cellular Component: microtubule; microtubule organizing center part; nuclear chromosome

Biological Context

Biological Process: meiotic spindle organization; microtubule organizing center organization
Molecular Function: GTPase activity

Attribution

Names: Stephane Brunet; Julien Dumont; Karen W. Lee; Kazuhisha Kinoshita; Pascale Hikal; Oliver J. Gruss; Bernard Maro; Marie-Helene Verlhac
Pubmed: 18833336
Link: http://www.plosone.org/article/info:doi%2F10....

Citation

Digital Object Identifier (DOI): doi:10.7295/W9CIL35431
Archival Resource Key (ARK): ark:/b7295/w9cil35431

Grouping This image is part of a group.

Imaging

Image Type: recorded image
Image Mode: confocal microscopy
Parameters Imaged: fluorescence emission
Source of Contrast: distribution of epitope
Visualization Methods: primary antibody plus labeled secondary antibody
Processing History: unprocessed raw data
Data Qualifiers: raw, unprocessed data; suitable for spatial measurements

Sample Preparation

Methods: chemically fixed tissue
Relation To Intact Cell: dispersed cells in vitro

Dimensions

Spatial Axis	Image Size	Pixel Size
X	1310px	0.1µm
Y	310px	0.1µm