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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear all, A colleague of mine experienced a special bleaching problem. A specific fusion construct of EGFP showed very rapid bleaching compared to unfused EGFP. I know that the overall brightness of fusions is often significant lower than of unfused EGFP (which was also true inher case) but I was not aware of such a bleach-specific difference. Can these be explained by unsufficient/partial folding of the EGFP within the fusion. In that case I d recommend to her to use superfolderGFP instead but I just wonder whether that explanation makes any sense to you? Many thanx! *********************** Martin Offterdinger, PhD Medical University Innsbruck Biocenter Division of Neurobiochemistry Biooptics Fritz-Pregl-Strasse 3 A-6010 Innsbruck Austria *********************** http://www.i-med.ac.at/neurobiochemistry/neurobiochemistry/Biooptics/Main.html |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I'm no expert in this field but I think any meaningful answer would require knowledge of what the construct was. As an extreme example, if you conjugated eGFP to a peroxidase you could probably expect this. Guy Optical Imaging Techniques in Cell Biology by Guy Cox CRC Press / Taylor & Francis http://www.guycox.com/optical.htm ______________________________________________ Associate Professor Guy Cox, MA, DPhil(Oxon) Australian Centre for Microscopy & Microanalysis, Madsen Building F09, University of Sydney, NSW 2006 Phone +61 2 9351 3176 Fax +61 2 9351 7682 Mobile 0413 281 861 ______________________________________________ http://www.guycox.net -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Martin Offterdinger Sent: Thursday, 29 September 2011 7:08 PM To: [hidden email] Subject: GFP bleaching: folding problem? ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear all, A colleague of mine experienced a special bleaching problem. A specific fusion construct of EGFP showed very rapid bleaching compared to unfused EGFP. I know that the overall brightness of fusions is often significant lower than of unfused EGFP (which was also true inher case) but I was not aware of such a bleach-specific difference. Can these be explained by unsufficient/partial folding of the EGFP within the fusion. In that case I d recommend to her to use superfolderGFP instead but I just wonder whether that explanation makes any sense to you? Many thanx! *********************** Martin Offterdinger, PhD Medical University Innsbruck Biocenter Division of Neurobiochemistry Biooptics Fritz-Pregl-Strasse 3 A-6010 Innsbruck Austria *********************** http://www.i-med.ac.at/neurobiochemistry/neurobiochemistry/Biooptics/Mai n.html ----- No virus found in this message. Checked by AVG - www.avg.com Version: 10.0.1410 / Virus Database: 1520/3925 - Release Date: 09/28/11 |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** The construct was not targeted to any organelle or so I don't know the details but it was not something very unususal at the first glimpse. martin |
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