Gabor Steinbach |
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http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal Dear LSM User, I am turning to you on behalf of a small spin-off company, associated with the Biological Research Center (BRC) of the Hungarian Academy of Sciences, Szeged. As part of our market research, we would like to ask your opinion on the possible use of polarization spectroscopic tools in LSMs. Please kindly fill in and return to us the following short questionnaire (put a + or x sign): Do you use polarized light in LSM imaging? [ ] Yes [ ] No Are you interested in imaging differential polarization quantities? [ ] Yes [ ] No If yes, please indicate importance (0: do not know, 1 not important, 5: very important) [ ] LD (linear dichroism) [ ] FDLD (fluorescence detected linear dichroism) [ ] r (anisotropy of the emitted light – upon non-polarized excitation) [ ] P (degree of polarization of the fluorescence) [ ] LB (linear birefringence) [ ] CD (circular dichroism) [ ] FDCD (fluorescence detected circular dichroism) [ ] CPL (circular polarization of luminescence) [ ] other, please specify: ............. Would you like to know more about DP measurements in (confocal) LSMs? [ ] Yes [ ] No Please describe your field of interest and the problem in which polarization and/or DP imaging might be of use: ............ Thank you for your help, please send your answers/comments to [hidden email] For more information DP imaging, including biological applications, please visit the website: www.brc.hu/dplsm Sincerely yours, Prof Gyozo Garab, Dr. Istvan Pomozi, Gabor Steinbach Biological Research Center Szeged, Hungary |
Nina Allen |
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http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal On 9/26/07 11:43 AM, "Gabor Steinbach" <[hidden email]> wrote: > Search the CONFOCAL archive at > http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal > > Dear LSM User, > > I am turning to you on behalf of a small spin-off company, associated > with the Biological > Research Center (BRC) of the Hungarian Academy of Sciences, Szeged. > As part of our market research, we would like to ask your opinion on the > possible use > of polarization spectroscopic tools in LSMs. > > Please kindly fill in and return to us the following short questionnaire > (put a + or x sign): > > Do you use polarized light in LSM imaging? > [x ] Yes > [ ] No > > Are you interested in imaging differential polarization quantities? > [ ] Yes > [x ] No > > If yes, please indicate importance (0: do not know, 1 not important, 5: > very important) > [ ] LD (linear dichroism) > [ ] FDLD (fluorescence detected linear dichroism) > [ ] r (anisotropy of the emitted light upon non-polarized excitation) > [ ] P (degree of polarization of the fluorescence) > [ ] LB (linear birefringence) > [ ] CD (circular dichroism) > [ ] FDCD (fluorescence detected circular dichroism) > [ ] CPL (circular polarization of luminescence) > [ ] other, please specify: ............. > > Would you like to know more about DP measurements in (confocal) LSMs? > [ ] Yes > [ x] No > > Please describe your field of interest and the problem in which > polarization and/or DP imaging might be of use: > .I am about to retire...would be interested in knowing what you are working on > > Thank you for your help, please send your answers/comments to [hidden email] > For more information DP imaging, including biological applications, > please visit the website: www.brc.hu/dplsm > > Sincerely yours, > Prof Gyozo Garab, Dr. Istvan Pomozi, Gabor Steinbach > Biological Research Center > Szeged, Hungary > Nina Stromgren Allen Professor, Department of Plant Biology Director, Cellular and Molecular Imaging Facility Past Chair of the Faculty North Carolina State University Raleigh, NC 27695-7612 919-515-3525, 5-8382,5-2279 |
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