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Date: | Fri, 16 Jan 2004 14:45:54 -0800 |
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Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
Shagufta-
What are you fixing with? Is it possible that your fluorescent
protein is going away during fixation?
Carol Heckman
>Search the CONFOCAL archive at
>http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>
> hi,
> I am using ERDsRED (from clontech)with EGFP tagged
>protein in a co-transfection for a co-localization
>study. The expression of my EGFP tagged protein is
>good enough to be easily captured by confocal
>microscope (as observed in separate experiments as
>well as a control to monitor the expression of EGFP
>tagged protein while doing co-transfection). However,
>after the co-transfection it is difficult for me to
>identify cells with both green and red fluorescence.
>In an epifluorescence microscope when i look for the
>co-transfected cells, under the blue light, they
>appear orange, which could be because of only the red
>fluorescence as similar orange fluorescence I observe
>with the control i.e. only ERDsRed transfected cells.
>In the co-transfected cells I do not see any green
>fluorescence. Is it that the fluorescence from ERDsRed
>is masking the expression of EGFP tagged protein? also
>why a red protein (ERDsRED)is getting excited by a
>blue light.
>
> please kindly send in your suggestions.
>Thaking you,
>Shagufta Rehman
>Ph.D. student
>Dept of Pathology
>AIIMS, New Delhi
>India.
>
>
>
>
>
>
>________________________________________________________________________
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--
__
Carol A. Heckman, Ph.D.
Professor of Biological Sciences
Director, Center for Microscopy & Microanalysis
Bowling Green State University, Bowling Green, OH 43403
fax: (419) 372-2024 email: [log in to unmask]
___________________________________________________________________________
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