Maria Y. Boulina |
*****
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 Microscopists, I need your opinions!! I am considering replacing a regular xcite with the LED unit on an old widefield Nikon TE2000. How does the LED-generated light intensity compare to that from an old-school light source? Which make should I consider: Thorlab, Lumen, Cool Light? I am very grateful to all contributors, thank you for your time!!! |
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. ***** What wavelengths do you need? Currently LEDs are a bit weak in UV production. If all you need is a white light then LEDs are very good. If you need fluorescence with different specific excitation bands then you have to be more cautious. Craig On Wed, Dec 17, 2014 at 11:30 AM, Maria Y. Boulina <[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 Microscopists, > I need your opinions!! I am considering replacing a regular xcite with > the LED unit on an > old widefield Nikon TE2000. How does the LED-generated light intensity > compare to that > from an old-school light source? Which make should I consider: Thorlab, > Lumen, Cool Light? > I am very grateful to all contributors, thank you for your time!!! > |
Cameron, Lisa |
I have a Lumencor Sola (white light version) and use it in combination with filter sets in the microscope turret.
It's working well with plenty of signal for routine fluorescence, usually set at approximately 1/3 the total output power or less. Some people have found their samples bleach faster compared to the Xcite we had before. No need for shutter or bulb changes anymore! No commercial interest. -Lisa --------------------------------------- Lisa Cameron Confocal and Light Microscopy Core Dana Farber Cancer Institute 450 Brookline Ave.; JF 621 Boston, MA -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Craig Brideau Sent: Wednesday, December 17, 2014 3:57 PM To: [hidden email] Subject: Re: [CONFOCALMICROSCOPY] LED lightsource vs classic xcite ***** 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. ***** What wavelengths do you need? Currently LEDs are a bit weak in UV production. If all you need is a white light then LEDs are very good. If you need fluorescence with different specific excitation bands then you have to be more cautious. Craig On Wed, Dec 17, 2014 at 11:30 AM, Maria Y. Boulina <[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 Microscopists, > I need your opinions!! I am considering replacing a regular xcite > with the LED unit on an old widefield Nikon TE2000. How does the > LED-generated light intensity compare to that from an old-school light > source? Which make should I consider: Thorlab, Lumen, Cool Light? > I am very grateful to all contributors, thank you for your time!!! > The information in this e-mail is intended only for the person to whom it is addressed. If you believe this e-mail was sent to you in error and the e-mail contains patient information, please contact the Partners Compliance HelpLine at http://www.partners.org/complianceline . If the e-mail was sent to you in error but does not contain patient information, please contact the sender and properly dispose of the e-mail. |
Maria Y. Boulina |
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. ***** I will need a standard set - 488, 555, 561, 594, maybe 633 range (users have not decided if they wanted the cube yet). All we image in UV is DAPI. But I thought that there is an array, and LEDs come in every flavour. 2014-12-17 15:57 GMT-05:00 Craig Brideau <[hidden email]>: > > ***** > 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. > ***** > > What wavelengths do you need? Currently LEDs are a bit weak in UV > production. If all you need is a white light then LEDs are very good. If > you need fluorescence with different specific excitation bands then you > have to be more cautious. > > Craig > > > On Wed, Dec 17, 2014 at 11:30 AM, Maria Y. Boulina <[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 Microscopists, > > I need your opinions!! I am considering replacing a regular xcite with > > the LED unit on an > > old widefield Nikon TE2000. How does the LED-generated light intensity > > compare to that > > from an old-school light source? Which make should I consider: Thorlab, > > Lumen, Cool Light? > > I am very grateful to all contributors, thank you for your time!!! > > > |
Barbara Foster |
In reply to this post by Maria Y. Boulina
*****
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, Marie A tool which I found useful is Semrock's Searchlight (http://www.semrock.com/searchlight-welcome.aspx). I used their graphs to compare the intensity of light sources for the American Lab article, Fluorescence: Fundamentals and Resources (to access a copy of the PDF, visit The Library at our site: http://microscopyeducation.com/inthelibrary/articles.html). Searchlight gives the spectral distributions for a number of the commonly available LED sources. Good hunting! Barbara Foster, President & Chief Consultant Microscopy/Microscopy Education* www.MicroscopyEducation.com *A subsidiary of The Microscopy & Imaging Place, Inc. 7101 Royal Glen Trail, Suite A McKinney, TX 75070 P: 972-924-5310 F: 214-592-0277 MME is currently scheduling courses for now and through June 2015. Call us today for a free training evaluation. At 03:41 PM 12/17/2014, you 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 Microscopists, >I need your opinions!! I am considering replacing a regular xcite >with the LED unit on an >old widefield Nikon TE2000. How does the LED-generated light >intensity compare to that >from an old-school light source? Which make should I consider: >Thorlab, Lumen, Cool Light? >I am very grateful to all contributors, thank you for your time!!! |
In reply to this post by Maria Y. Boulina
*****
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. ***** Great to see this discussion going on as LED illumination systems become more and more mainstream. A point on Searchlight: unless you put specific power values in the advanced section then you cannot use it to compare power as most of the light source curves are either normalised to 100% or only relative to themselves rather than any particular value. Putting power values in is a challenge as there is no standard from the manufacturers on how to measure power and therefore no basis for a comparison other than try it! After evolution of LED solutions over the last few years it is generally found that intensities are now suitable for the majority of peoples needs. To be blatant, please have a look at www.coolled.com We offer a wide range from single wavelength through everyday but controllable white light and up to a very flexible high end (but not high price) solutions. Raj Patey CoolLED Ltd. |
*****
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 Marie, when switching from Arc-lamp to LED, you might want to change some of your excitation filters, in particular those that make use of the peaks of the Hg- or mixed gas arc--lamps (like X-cite) in the near UV and around 550nm. LEDs have many advantages. I posted earlier that I have made excellent experience with CoolLed, and no commercial interest. Buying a new lamp, I would always prefer LED instead of Arc. Happy imaging! Jens http://br.linkedin.com/pub/jens-rietdorf/6/4a3/189/ Skype jens.rietdorf On Thu, Dec 18, 2014 at 7:53 AM, Raj Patey <[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. > ***** > > Great to see this discussion going on as LED illumination systems become > more > and more mainstream. > > A point on Searchlight: unless you put specific power values in the > advanced > section then you cannot use it to compare power as most of the light > source curves > are either normalised to 100% or only relative to themselves rather than > any > particular value. Putting power values in is a challenge as there is no > standard > from the manufacturers on how to measure power and therefore no basis for a > comparison other than try it! After evolution of LED solutions over the > last few > years it is generally found that intensities are now suitable for the > majority of > peoples needs. > > To be blatant, please have a look at www.coolled.com We offer a wide > range from > single wavelength through everyday but controllable white light and up to > a very > flexible high end (but not high price) solutions. > > Raj Patey > CoolLED Ltd. > |
In reply to this post by Maria Y. Boulina
*****
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. ***** On Wed, 17 Dec 2014 16:38:32 -0500, Marcia Boulina <[hidden email]> wrote: >I will need a standard set - 488, 555, 561, 594, maybe 633 range (users >have not decided if they wanted the cube yet). All we image in UV is DAPI. >But I thought that there is an array, and LEDs come in every flavour. We have a Lumencor SpectraX on our TE2000 and we love it. We bought one new Chroma quad-band dichroic and emission filter set, as well as 4 separate single- band emission filters for our emission filter wheel (although this latter set is not absolutely necessary). The amazing thing is to be able to run color sequences at the frame rate of the camera (because the SpectraX accepts TTL triggering of each line independently). It is beautiful to see the rainbow of light flashing out of the scope at 20+ frames per second! https://micro-manager.org/wiki/Hardware-based_synchronization We use a ESio TTL box controlled by Micro-Manager and it works great. But you could use an Arduino and some wiring to accomplish the same thing for cheaper. We haven't run into any issues with brightness: the SpectraX is bright enough for all our cell imaging experiments. Typically, we run it at 20% power. That said, I'm aware that the very bright peaks in an arc lamp spectrum (e.g. UV, 435, 546) aren't there in the LED spectra. So for FRAP or something, you may not be able to bleach as fast. -Sam |
Periasamy, Ammasi (ap3t) |
In reply to this post by Raj Patey
*****
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. ***** I would check out the new X-Cite LEDs. There are 2 versions: 120LED (direct coupled) and 110LED (liquid light guide). I have used only the 120led and found it to do the job just fine. The main thing for me is the company is reliable and has been around for a long time... http://www.excelitas.com/Pages/Product/X-Cite-110LED.aspx No financial interest.... Dr. Ammasi Periasamy Professor & Center Director http://www.kcci.virginia.edu/contact/peri.php Office Location W.M. Keck Center for Cellular Imaging Physical and Life Sciences Building, (B 005) At the intersection of Geldard dr and White head Rd., Phone: (434) 243-7602 or 982-4869 Fax: (434) 982-5210 E-mail: [hidden email] Messenger Mail: P.O. Box 400328 Mailing or Shipping Address: W.M. Keck Center for Cellular Imaging (PLSB 005) University of Virginia Biology, Gilmer Hall, 485 McCormick Rd. Charlottesville, VA 22904, USA FRET Workshop: http://www.kcci.virginia.edu/workshop/index.php -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Raj Patey Sent: Thursday, December 18, 2014 4:53 AM To: [hidden email] Subject: Re: LED lightsource vs classic xcite ***** 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. ***** Great to see this discussion going on as LED illumination systems become more and more mainstream. A point on Searchlight: unless you put specific power values in the advanced section then you cannot use it to compare power as most of the light source curves are either normalised to 100% or only relative to themselves rather than any particular value. Putting power values in is a challenge as there is no standard from the manufacturers on how to measure power and therefore no basis for a comparison other than try it! After evolution of LED solutions over the last few years it is generally found that intensities are now suitable for the majority of peoples needs. To be blatant, please have a look at www.coolled.com We offer a wide range from single wavelength through everyday but controllable white light and up to a very flexible high end (but not high price) solutions. Raj Patey CoolLED Ltd. |
Free forum by Nabble | Edit this page |