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Hello,
I would like to count cells in two channel confocal stacks. To better perform the counting of double labelled cells I would like to switch between red and green view to an only red or only green view. With photosohop there is a channel window that enables you to switch on and off the R, B or G channel. Anybody knows whether there Is something similar in imageJ? Being able to look at the two staining either separated or merged is essential for judging if a structure is single or double labelled..
Thank you
Federico
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