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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hello All, We are buying a new confocal/epi microscope. And are interested in experience of users with the CoolLED system. Do you recommend the CoolLED system over a metal halide lamp? We want to use the system with epi fluorescence of live cells with Hoechst, GFP and Cy3 channels. Thanks, Hans de Bont Dept of Toxicology LACDR University of Leiden Einsteinweg 55 2333 CC Leiden The Netherlands Tel: 071-5274496 Mobile: 06-11351598 |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hello Hans, We have/had very good experiences with the CoolLed, so I'd not hesitate too much to go with it. Its only weakness is that it offers less intensity then a typical (strong) metal-halide lamp. This may be a problem if you use low NA low mag.oObjectives. For the 63x or 40x oil-immersion typically used on a confocal this is not an issue. Cheers Gabor Light Microscopy Centre ETH Zurich, Schafmattstrasse 18 CH-8093, Zurich Switzerland Phone: +41 44 633 6221 On 6/29/11 9:56 AM, "H. de Bont" <[hidden email]> wrote: >***** >To join, leave or search the confocal microscopy listserv, go to: >http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >***** > >Hello All, > > > >We are buying a new confocal/epi microscope. > > > >And are interested in experience of users with the CoolLED system. > >Do you recommend the CoolLED system over a metal halide lamp? > >We want to use the system with epi fluorescence of live cells with >Hoechst, >GFP and Cy3 channels. > > > > > >Thanks, > > > >Hans de Bont > >Dept of Toxicology > >LACDR > >University of Leiden > >Einsteinweg 55 > >2333 CC Leiden > >The Netherlands > >Tel: 071-5274496 > >Mobile: 06-11351598 > > |
In reply to this post by H. de Bont
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Hans, Basically, same answer as Gabor... We are happy with ours. We have CoolLEDs both on our confocals (for visual inspection, this is more than sufficient) and on some of our wide-field live cell imaging setups. Intensity is lower than a strong metal halide light, but with live cells you want anyhow to avoid photobleaching and photodamage... Best regards, Laurent. ___________________________ Laurent Gelman, PhD Friedrich Miescher Institut Facility for Advanced Imaging and Microscopy WRO 1066.2.16 Maulbeerstrasse 66 CH-4058 Basel +41 (0)79 618 73 69 -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of H. de Bont Sent: mercredi 29 juin 2011 09:56 To: [hidden email] Subject: CoolLED ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hello All, We are buying a new confocal/epi microscope. And are interested in experience of users with the CoolLED system. Do you recommend the CoolLED system over a metal halide lamp? We want to use the system with epi fluorescence of live cells with Hoechst, GFP and Cy3 channels. Thanks, Hans de Bont Dept of Toxicology LACDR University of Leiden Einsteinweg 55 2333 CC Leiden The Netherlands Tel: 071-5274496 Mobile: 06-11351598 |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Have you tried IRM with the CoolLED system? Thanks! -Michael _________________________________________ Michael Cammer, Assistant Research Scientist Skirball Institute of Biomolecular Medicine Lab: (212) 263-3208 Cell: (914) 309-3270 -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Gelman, Laurent Sent: Friday, July 01, 2011 8:54 AM To: [hidden email] Subject: Re: CoolLED ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Hans, Basically, same answer as Gabor... We are happy with ours. We have CoolLEDs both on our confocals (for visual inspection, this is more than sufficient) and on some of our wide-field live cell imaging setups. Intensity is lower than a strong metal halide light, but with live cells you want anyhow to avoid photobleaching and photodamage... Best regards, Laurent. ___________________________ Laurent Gelman, PhD Friedrich Miescher Institut Facility for Advanced Imaging and Microscopy WRO 1066.2.16 Maulbeerstrasse 66 CH-4058 Basel +41 (0)79 618 73 69 -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of H. de Bont Sent: mercredi 29 juin 2011 09:56 To: [hidden email] Subject: CoolLED ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hello All, We are buying a new confocal/epi microscope. And are interested in experience of users with the CoolLED system. Do you recommend the CoolLED system over a metal halide lamp? We want to use the system with epi fluorescence of live cells with Hoechst, GFP and Cy3 channels. Thanks, Hans de Bont Dept of Toxicology LACDR University of Leiden Einsteinweg 55 2333 CC Leiden The Netherlands Tel: 071-5274496 Mobile: 06-11351598 ------------------------------------------------------------ This email message, including any attachments, is for the sole use of the intended recipient(s) and may contain information that is proprietary, confidential, and exempt from disclosure under applicable law. Any unauthorized review, use, disclosure, or distribution is prohibited. If you have received this email in error please notify the sender by return email and delete the original message. Please note, the recipient should check this email and any attachments for the presence of viruses. The organization accepts no liability for any damage caused by any virus transmitted by this email. ================================= |
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