Csúcs Gábor-3 |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Dear All, Linked to a user request, I have a relatively unusual question: instead of a photostable dye, we are looking for an unstable (very sensitive one). The excitation wavelength should be around 395 nm. The user would like to create free radicals in a spatially localized manner (as a result of photobleaching dyes). Does anyone have a suggestion? Greetings Gabor |
Craig Brideau |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Rose Bengal might work. It usually wants green excitation, but might work with 395nm as well. Craig On Wed, Jan 18, 2017 at 10:26 AM, Csúcs Gábor <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > Post images on http://www.imgur.com and include the link in your posting. > ***** > > Dear All, > > Linked to a user request, I have a relatively unusual question: instead of > a photostable dye, we are looking for an unstable (very sensitive one). The > excitation wavelength should be around 395 nm. The user would like to > create free radicals in a spatially localized manner (as a result of > photobleaching dyes). Does anyone have a suggestion? > > Greetings Gabor > |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Does it have to be a fluorophore? If not, I would search for photosensitizers -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Craig Brideau Sent: Wednesday, January 18, 2017 12:53 PM To: [hidden email] Subject: Re: Photosensitive, 395nm excitable dye ***** To join, leave or search the confocal microscopy listserv, go to: https://na01.safelinks.protection.outlook.com/?url=http%3A%2F%2Flists.umn.edu%2Fcgi-bin%2Fwa%3FA0%3Dconfocalmicroscopy&data=01%7C01%7Cmmodel%40KENT.EDU%7C728ebff364154c2614b508d43fcaed6d%7Ce5a06f4a1ec44d018f73e7dd15f26134%7C1&sdata=dh3SeORLcZVoMXB5kCtVMgyq0zeJCPYWfVqDr27CkKs%3D&reserved=0 Post images on https://na01.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.imgur.com&data=01%7C01%7Cmmodel%40KENT.EDU%7C728ebff364154c2614b508d43fcaed6d%7Ce5a06f4a1ec44d018f73e7dd15f26134%7C1&sdata=5JN%2BukM6SLCMMEBnVoYbqhd4xN0ewGnbRg0ySlLm5FE%3D&reserved=0 and include the link in your posting. ***** Rose Bengal might work. It usually wants green excitation, but might work with 395nm as well. Craig On Wed, Jan 18, 2017 at 10:26 AM, Csúcs Gábor <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > https://na01.safelinks.protection.outlook.com/?url=http%3A%2F%2Flists. > umn.edu%2Fcgi-bin%2Fwa%3FA0%3Dconfocalmicroscopy&data=01%7C01%7Cmmodel > %40KENT.EDU%7C728ebff364154c2614b508d43fcaed6d%7Ce5a06f4a1ec44d018f73e > 7dd15f26134%7C1&sdata=dh3SeORLcZVoMXB5kCtVMgyq0zeJCPYWfVqDr27CkKs%3D&r > eserved=0 Post images on > https://na01.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.imgur.com&data=01%7C01%7Cmmodel%40KENT.EDU%7C728ebff364154c2614b508d43fcaed6d%7Ce5a06f4a1ec44d018f73e7dd15f26134%7C1&sdata=5JN%2BukM6SLCMMEBnVoYbqhd4xN0ewGnbRg0ySlLm5FE%3D&reserved=0 and include the link in your posting. > ***** > > Dear All, > > Linked to a user request, I have a relatively unusual question: > instead of a photostable dye, we are looking for an unstable (very > sensitive one). The excitation wavelength should be around 395 nm. The > user would like to create free radicals in a spatially localized > manner (as a result of photobleaching dyes). Does anyone have a suggestion? > > Greetings Gabor > |
Iain Johnson |
In reply to this post by Csúcs Gábor-3
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** If you just want the dye to be photoxic and not fluorescent, a chlorin or porphyrin-based photosensitizer would likely work well. These are compounds optimized and routinely used for photodynamic therapy. They have very strong absorption peaks (extinction ~400,000 cm-1 M-1) at about 415 nm. Foscan (aka Temporfin) is one such compound. Cayman Chemical sells it in amounts and at prices suitable for research applications. Iain On Wed, Jan 18, 2017 at 9:26 AM, Csúcs Gábor <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > Post images on http://www.imgur.com and include the link in your posting. > ***** > > Dear All, > > Linked to a user request, I have a relatively unusual question: instead of > a photostable dye, we are looking for an unstable (very sensitive one). The > excitation wavelength should be around 395 nm. The user would like to > create free radicals in a spatially localized manner (as a result of > photobleaching dyes). Does anyone have a suggestion? > > Greetings Gabor > |
In reply to this post by Craig Brideau
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Hi Gabor, Chlorins have an absorption peak at 350-450nm. DOI: 10.1039/C3PP50376C (Paper) Photochem. Photobiol. Sci., 2014, 13, 1137-1145 Abraços, Jens Dr. Jens Rietdorf, visiting scientist @ center for technological development in health CDTS, Oswaldo Cruz Foundation Fiocruz, Rio de Janeiro Brasil. On Wed, Jan 18, 2017 at 3:53 PM, Craig Brideau <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > Post images on http://www.imgur.com and include the link in your posting. > ***** > > Rose Bengal might work. It usually wants green excitation, but might work > with 395nm as well. > > Craig > > On Wed, Jan 18, 2017 at 10:26 AM, Csúcs Gábor <[hidden email]> > wrote: > > > ***** > > To join, leave or search the confocal microscopy listserv, go to: > > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > > Post images on http://www.imgur.com and include the link in your > posting. > > ***** > > > > Dear All, > > > > Linked to a user request, I have a relatively unusual question: instead > of > > a photostable dye, we are looking for an unstable (very sensitive one). > The > > excitation wavelength should be around 395 nm. The user would like to > > create free radicals in a spatially localized manner (as a result of > > photobleaching dyes). Does anyone have a suggestion? > > > > Greetings Gabor > > > |
George McNamara |
In reply to this post by Iain Johnson
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Hi Gabor, QDot 655 also makes O2 radicals: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095390/ Transl Stroke Res. <https://www.ncbi.nlm.nih.gov/pubmed/?term=A+protocol+for+characterizing+the+impact+of+collateral+flow+after+distal+middle+cerebral+artery+occlusion#>2011 Mar;2(1):112-27. doi: 10.1007/s12975-010-0044-2. A*protocol*for*characterizing*the*impact*of*collateral**flow**after**distal**middle**cerebral**artery**occlusion*. Defazio RA <https://www.ncbi.nlm.nih.gov/pubmed/?term=Defazio%20RA%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>^1 ,Levy S <https://www.ncbi.nlm.nih.gov/pubmed/?term=Levy%20S%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>,Morales CL <https://www.ncbi.nlm.nih.gov/pubmed/?term=Morales%20CL%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>,Levy RV <https://www.ncbi.nlm.nih.gov/pubmed/?term=Levy%20RV%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>,Dave KR <https://www.ncbi.nlm.nih.gov/pubmed/?term=Dave%20KR%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>,Lin HW <https://www.ncbi.nlm.nih.gov/pubmed/?term=Lin%20HW%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>,Abaffy T <https://www.ncbi.nlm.nih.gov/pubmed/?term=Abaffy%20T%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>,Watson BD <https://www.ncbi.nlm.nih.gov/pubmed/?term=Watson%20BD%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>,Perez-Pinzon MA <https://www.ncbi.nlm.nih.gov/pubmed/?term=Perez-Pinzon%20MA%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>,Ohanna V <https://www.ncbi.nlm.nih.gov/pubmed/?term=Ohanna%20V%5BAuthor%5D&cauthor=true&cauthor_uid=21593993>. Author information<https://www.ncbi.nlm.nih.gov/pubmed/?term=A+protocol+for+characterizing+the+impact+of+collateral+flow+after+distal+middle+cerebral+artery+occlusion#> Abstract In humans and in animal models of stroke,*collateral*blood*flow*between territories of the major pial arteries has a profound*impact*on cortical infarct size. However, there is a gap in our understanding of the genetic determinants of*collateral*formation and*flow*, as well as the signaling pathways and neurovascular interactions regulating this*flow*. Previous studies have demonstrated that*collateral**flow*between branches of the anterior*cerebral**artery*(ACA) and the*middle**cerebral**artery*(MCA) can protect mouse cortex from infarction*after**middle**cerebral**artery**occlusion*. Because the number and diameter of collaterals varies among mouse strains and*after*transgenic manipulations, a combination of methods is required to control for these variations. Here, we report an inexpensive approach to*characterizing*the cerebrovascular anatomy, and in vivo monitoring of*cerebral*blood*flow*as well. Further, we introduce a new, minimally invasive method for the*occlusion*of*distal*MCA branches. These methods will permit a new generation of studies on the mechanisms regulating*collateral*remodeling and cortical blood*flow**after*stroke. PMID: 21593993 PMCID: PMC3095390 <https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095390/> DOI: 10.1007/s12975-010-0044-2 <https://dx.doi.org/10.1007/s12975-010-0044-2> On 1/19/2017 12:00 AM, Iain Johnson wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > Post images on http://www.imgur.com and include the link in your posting. > ***** > > If you just want the dye to be photoxic and not fluorescent, a chlorin or > porphyrin-based photosensitizer would likely work well. These are > compounds optimized and routinely used for photodynamic therapy. They have > very strong absorption peaks (extinction ~400,000 cm-1 M-1) at about 415 > nm. Foscan (aka Temporfin) is one such compound. Cayman Chemical sells it > in amounts and at prices suitable for research applications. > > Iain > > On Wed, Jan 18, 2017 at 9:26 AM, Csúcs Gábor <[hidden email]> > wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> Post images on http://www.imgur.com and include the link in your posting. >> ***** >> >> Dear All, >> >> Linked to a user request, I have a relatively unusual question: instead of >> a photostable dye, we are looking for an unstable (very sensitive one). The >> excitation wavelength should be around 395 nm. The user would like to >> create free radicals in a spatially localized manner (as a result of >> photobleaching dyes). Does anyone have a suggestion? >> >> Greetings Gabor >> -- George McNamara, PhD Houston, TX 77054 [hidden email] https://www.linkedin.com/in/georgemcnamara https://works.bepress.com/gmcnamara/75/ http://www.ncbi.nlm.nih.gov/myncbi/browse/collection/44962650 |
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