CONFOCALMICROSCOPY Archives

June 2015

CONFOCALMICROSCOPY@LISTS.UMN.EDU

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From:
Mike Tighe <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Tue, 30 Jun 2015 14:37:51 +0000
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would anybody know if it is possible to import a 3 or 4 color image into imageJ and have the software locate cells or objects that have signal in all or some of those channels? For example I have one channel for CD8 Tcells and I would like to have the software show me which of those CD8's are positive in one or two other channels. Rather than doing this manually.

Thanks for any help!!
Mike

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