Acta Stereologica

0351-580X

 

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Richard Delorme, Catherine Souchier & Paul-André Bryon

A three dimensional quantitative approach for colocalization study of cyclin A and P34cdk1 by confocal microscopy

(Volume 14 (1995) — Number 2 - Quantitative image analysis - Nov. 1995)
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Abstract

In mammalian cells, cyclin A and cyclin B are known to regulate P34cdkl activity during the entry into mitosis, whereas cyclin A also regulates p33cdk2 kinase. Confocal laser scanning microscopy acquisition and three dimensional image analysis were performed to quantitatively estimate cyclin A and P34cdk1 colocalization on lymphoid RAMOS cell line. Cytofluorograms were used to derive parameters estimating colocalization. Colocalization globally increased when cells accumulated cyclin A. However, results demonstrated that some positive voxels were not colocalized.

Keywords : colocalization, confocal microscopy, cyclin A, double labelling, image analysis, P34cdk1

Om dit artikel te citeren:

Richard Delorme, Catherine Souchier & Paul-André Bryon, «A three dimensional quantitative approach for colocalization study of cyclin A and P34cdk1 by confocal microscopy», Acta Stereologica [En ligne], Volume 14 (1995), Number 2 - Quantitative image analysis - Nov. 1995, 155-160 URL : https://popups.uliege.be/0351-580x/index.php?id=816.

Over : Richard Delorme

Laboratoire de Cytologie Analytique, Université Claude-Bernard Lyoni, 8 avenue Rockefeller, 69373 Lyon CEDEX 08, France

Over : Catherine Souchier

Laboratoire de Cytologie Analytique, Université Claude-Bernard Lyoni, 8 avenue Rockefeller, 69373 Lyon CEDEX 08, France

Over : Paul-André Bryon

Laboratoire de Cytologie Analytique, Université Claude-Bernard Lyoni, 8 avenue Rockefeller, 69373 Lyon CEDEX 08, France