G. Esteban Fernandez |
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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 all, 1) I'm curious how much time, roughly, it takes for a Peltier-cooled CCD camera to reach the lowest temperature. Are we talking a few minutes or closer to an hour or more? I have several brands of cooled CCDs of different vintages and I'm just looking for a "rule of thumb", if possible. 2) I do plan to test my cameras myself: I was thinking of imaging a timelapse of a dim & stable specimen (requiring something like 30-60 sec. exposure) after turning cooling on to see at what time noise reaches a minimum. Any suggestions for other ways to test this are welcome. Thanks, Esteban |
Nico Stuurman |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** On May 12, 2012, at 2:28 PM, G. Esteban Fernandez wrote: > 1) I'm curious how much time, roughly, it takes for a Peltier-cooled > CCD camera to reach the lowest temperature. Are we talking a few > minutes or closer to an hour or more? I have several brands of cooled > CCDs of different vintages and I'm just looking for a "rule of thumb", > if possible. Our EM CCDs (from Hamamatsu and Andor) cool to -70 C in a few minutes. The build-in sensor's temperature can be read-out through software. Best, Nico |
David Baddeley |
In reply to this post by G. Esteban Fernandez
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Most modern cameras reach their temperature setpoint within about 5 mins (some are considerably faster). You can generally read the temperature out through software, and don't need to rely on measuring the noise. If you do measure noise, keep in mind that the baseline also tends to change with temperature. Cheers, David ------------------------------ On Sun, May 13, 2012 9:28 AM NZST G. Esteban Fernandez wrote: >***** >To join, leave or search the confocal microscopy listserv, go to: >http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >***** > >Hi all, > >1) I'm curious how much time, roughly, it takes for a Peltier-cooled >CCD camera to reach the lowest temperature. Are we talking a few >minutes or closer to an hour or more? I have several brands of cooled >CCDs of different vintages and I'm just looking for a "rule of thumb", >if possible. > >2) I do plan to test my cameras myself: I was thinking of imaging a >timelapse of a dim & stable specimen (requiring something like 30-60 >sec. exposure) after turning cooling on to see at what time noise >reaches a minimum. Any suggestions for other ways to test this are >welcome. > >Thanks, >Esteban |
Paul Herzmark |
In reply to this post by G. Esteban Fernandez
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Esteban, I am curious what kind of sample you expose for 30-60 seconds? Won't background fluorescence kill you? Paul Herzmark Department of Molecular and Cell Biology University of California, Berkeley On Sat, May 12, 2012 at 2:28 PM, G. Esteban Fernandez < [hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Hi all, > > 1) I'm curious how much time, roughly, it takes for a Peltier-cooled > CCD camera to reach the lowest temperature. Are we talking a few > minutes or closer to an hour or more? I have several brands of cooled > CCDs of different vintages and I'm just looking for a "rule of thumb", > if possible. > > 2) I do plan to test my cameras myself: I was thinking of imaging a > timelapse of a dim & stable specimen (requiring something like 30-60 > sec. exposure) after turning cooling on to see at what time noise > reaches a minimum. Any suggestions for other ways to test this are > welcome. > > Thanks, > Esteban > |
George McNamara |
In reply to this post by G. Esteban Fernandez
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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 Esteban, As others have noted, cooling is pretty quick. You do NOT want to do this with a fluorescent specimen - you would be getting both photobleaching and camera cooling. Cooling affects the dark current, rule of thumb is dark current decreases with every ~7 C of cooling. A simple test - I'll use MetaMorph as an example: 1. Start everything, except the camera (MetaMorph will typically complain about the camera, just say no to try again). 2. Configure the exposure time to 1 ms (Acquire image command). 3. Create a journal and taskbar button to do Acquire Timelapse, say one exposure per second, 5 second interval, for (say) 15 minutes, to stack -- or disk if you want more data. Make the Taskbar visible so you can clikc on the journal button immediately after starting MetaMorph next time. 4. Setup the light path so NO LIGHT goes to the camera (or put the lens cap on). 5. Exit MetaMorph. 6. Turn on the camera, immediately start MetaMorph, click the journal button. When done, save the data. Simplest to use Apps - Graph Intensity, but Measure Regions is fine. 7. Go have lunch. 8. Close the stack or change the file save name and/or path. 9. Acquire another timelapse after the camera has fully cooled. On my ORCA-ER(s), starting intensity is around 300, takes a couple of minutes to reach ~200 (12-bit range). On my ORCA-II ERG, takes longer to cool to -60 C, offset when cool is ~600 out of 14-bit range. // Speaking of timelapse tests - the centenary of the discovery of cosmic ray particles by Victor Hess is 7 August 2012 (http://en.wikipedia.org/wiki/Cosmic_ray and M. Friedlander 2012 Nature 483: 400-401 do not currently give the date - date from P. Carlson 2012 Physics Today Feb 2012: 30-36). I encourage everyone with a camera that can be set to "no light" to do either a Friday August 3 (end of work) to Monday August 4 (start of work) or overnight(s) August 7. No light, max exposure time for your camera, continuous timelapse. Easiest way to summarize the dataset is to aet up your software to do a maximum between the newest image and an "accumulation" image (of course test this before the big date). I recently submitted a 30,000 frame (ORCA-ER, 10 second exposures) to one of the microscope company photo contests. As for what to do with the data - I suggested to one of my colleagues that they take the lead in posting this request to the listserv. I haven't seen a post from them (yet). If they decide not to organize everyone's image, perhaps Esteban will? If not, I'll consider making a montage of everyone's accumulation images for posting someplace on the Internet. George p.s. I am not a fan of N=1 experiments, so I want to credit M. Friedlander (Nature article) for pointing out that: "In 1932, Carl Anderson was using a Wilson cloud chamber with a large magnet to study cosmic rays when he observed a particle that had the mass of an electron, but a positive charge. The discovery of the positron, as Anderson named the particle, was recognized when Anderson shared the 1936 Nobel prize with Hess." On 5/12/2012 5:28 PM, G. Esteban Fernandez wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Hi all, > > 1) I'm curious how much time, roughly, it takes for a Peltier-cooled > CCD camera to reach the lowest temperature. Are we talking a few > minutes or closer to an hour or more? I have several brands of cooled > CCDs of different vintages and I'm just looking for a "rule of thumb", > if possible. > > 2) I do plan to test my cameras myself: I was thinking of imaging a > timelapse of a dim& stable specimen (requiring something like 30-60 > sec. exposure) after turning cooling on to see at what time noise > reaches a minimum. Any suggestions for other ways to test this are > welcome. > > Thanks, > Esteban > > |
G. Esteban Fernandez |
In reply to this post by Paul Herzmark
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Thanks for bringing that up Paul. I was thinking along the same lines so my plan was to go with a transmitted specimen, but that might not be possible if the TL bulb is not stable at very low brightness; I might have to get creative with the illumination. I don't even know if 30s is long enough exposure for dark current to dominate. Maybe I can use a bead slide and turn the fluorescence excitation way down (at the lamp and with the aperture diaphragm)? Suggestions for dim, nil background specimens are welcome! If cameras reach lowest temp. within a few minutes then practically speaking this is all moot, I'll just turn the cameras on 10 min. before imaging. But I'm still curious how much of an effect cooling has, and how long the exposure needs to be before cooling offers an advantage. I hear that thermal cycling is a problem (and in fact I have one camera where the cooling system died) so if cooling gets me nothing I'll just keep it off and turn it on only when needed. I guess I can calculate that from the noise specs, and I would if dark current w/o cooling were reported, but I'd still want to see for myself with data. -Esteban On Sat, May 12, 2012 at 6:02 PM, Paul Herzmark <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Esteban, > > I am curious what kind of sample you expose for 30-60 seconds? Won't > background fluorescence kill you? > > Paul Herzmark > Department of Molecular and Cell Biology > University of California, Berkeley > > > On Sat, May 12, 2012 at 2:28 PM, G. Esteban Fernandez < > [hidden email]> wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ***** >> >> Hi all, >> >> 1) I'm curious how much time, roughly, it takes for a Peltier-cooled >> CCD camera to reach the lowest temperature. Are we talking a few >> minutes or closer to an hour or more? I have several brands of cooled >> CCDs of different vintages and I'm just looking for a "rule of thumb", >> if possible. >> >> 2) I do plan to test my cameras myself: I was thinking of imaging a >> timelapse of a dim & stable specimen (requiring something like 30-60 >> sec. exposure) after turning cooling on to see at what time noise >> reaches a minimum. Any suggestions for other ways to test this are >> welcome. >> >> Thanks, >> Esteban >> |
Julio Vazquez |
In reply to this post by G. Esteban Fernandez
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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 Esteban, not sure why you would need a specimen at all..... I typically check cameras by taking several dark exposures at different exposure times (such as from 10 ms to 1 second) and look at the image histograms. This can be very informative, and will allow you to not only measure or estimate dark current and thermal noise, but will also show dark and hot pixels, and sometimes other funky things. If the camera has different read out modes or gain settings, it is also useful to test those. Taking varing exposures of an actual (ideally homogenous and non-bleaching) sample can give you additionla info, such as how linear the response of the camera (and/or individual pixels) is. We typically do that with fluorescent plexiglas slides. = Julio Vazquez Fred Hutchinson Cancer Research Center Seattle, WA 98109-1024 http://www.fhcrc.org == On May 12, 2012, at 2:28 PM, G. Esteban Fernandez wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Hi all, > > 1) I'm curious how much time, roughly, it takes for a Peltier-cooled > CCD camera to reach the lowest temperature. Are we talking a few > minutes or closer to an hour or more? I have several brands of cooled > CCDs of different vintages and I'm just looking for a "rule of thumb", > if possible. > > 2) I do plan to test my cameras myself: I was thinking of imaging a > timelapse of a dim & stable specimen (requiring something like 30-60 > sec. exposure) after turning cooling on to see at what time noise > reaches a minimum. Any suggestions for other ways to test this are > welcome. > > Thanks, > Esteban |
Csúcs Gábor |
In reply to this post by George McNamara
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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, I'd really appreciate if you could make potential candidates aware of the position advertised below. It is not directly a confocal microscopy related position (my excuse for that) but certainly very much linked to it. Thanks Gabor Head of the Data Analysis Unit for Light Microscopy and High Throughput Screening The Light Microscopy and Screening Centre (LMSC) of the ETH Zurich is one of the leading academic core facilities in Switzerland offering access to high-end microscopy and high-throughput screening instrumentation. Currently we have ~ 250 users mostly coming from the biology but including researchers also from physics, material science etc. Besides experimental instrumentation, the LMSC operates a number of image processing computers with various commercial and custom software packages. Being not only a service unit, the LMSC performs active research in various imaging related fields often in close collaboration with the different ETH departments (biology, computer science, engineering etc.) Due to strongly increasing demand, the LMSC will set up a new unit in order to support its users on the field of data analysis, covering biological image processing, instrument control, image-based modelling and simulation, data processing for high-throughput screening covering the complete analysis pipeline, also including classification, hit definition, statistical evaluation, maintaining screening databases and related bioinformatics tasks. Central mission of the Data Analysis Unit is to provide comprehensive service for the users of LMSC, including basic education and training in using various software tools and packages, helping to adapt existing and develop customized tools for solving individual data analysis problems as well as maintain joint research efforts aiming at developing new methods on areas of strategic importance for the LMSC community. We are looking for a scientist with proven research and/or service track on at least some of the fields mentioned above. S/he is expected to actively participate in and oversee the service and training activities (the primary function of the unit) while upon availability of resources also initiate research projects in close collaboration with LMSC users and supervise the participating Master´s and PhD students. S/he should start the operation of the unit immediately while building up the group to full-scale operation within the next 2 years, including recruiting further staff member(s) and fundraising for financing long-term development efforts. The suitable candidate is having a PhD degree in Computer Science/Physics/Biology or related field. Experience with ImageJ (Java) or Matlab is expected, C++, R and scripting is of advantage. Knowledge of databases and bioinformatics tools is a strong plus. Good communication skills (solid English knowledge) and willingness to participate in teaching activities at quite different levels are essential. Initial contract will be offered for one year but can be prolonged with a possibility of permanent employment. The ETH Zurich offers cutting-edge infrastructure, highly international environment and excellent working conditions. Please send your CV + publication list, including a short description of your current research interests and the name/address of potential references (in electronic format) to: Daniela Tschümperlin; [hidden email] Further information is available on www.lmc.ethz.ch <http://www.lmc.ethz.ch> or contact Dr. G. Csucs ([hidden email]). |
In reply to this post by G. Esteban Fernandez
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi, Esteban, I did this last year with one of my old CoolSnapHQs (~10 yrs now) which cool down to -30C. I can share some of the data (just couple of graphs and a movie show the cooling effects) with anyone who is interested by emailing me privately. Here is a brief summary of the finding: The camera is cooled down quickly. Within ~3-5mins, there is no more visible hot pixels. However, it takes ~20mins to stabilize (measuring average intensity, standard deviation and signal-noise ratio of the images). I tested another EMCCD which cools down to -70. It is faster but still needs about 10mins to stabilize. You just need to set up a timelapse imaging with all light to the camera blocked. It sounds easy but it takes several attempts to get it right as you need to start the camera from cold. Do as fast as you could because the cooling rate is pretty rapid and you miss the interesting part (first 2-3 mins). Best wishes, Xuejun -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of G. Esteban Fernandez Sent: Saturday, May 12, 2012 3:28 PM To: [hidden email] Subject: Cooling time for CCD cameras ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi all, 1) I'm curious how much time, roughly, it takes for a Peltier-cooled CCD camera to reach the lowest temperature. Are we talking a few minutes or closer to an hour or more? I have several brands of cooled CCDs of different vintages and I'm just looking for a "rule of thumb", if possible. 2) I do plan to test my cameras myself: I was thinking of imaging a timelapse of a dim & stable specimen (requiring something like 30-60 sec. exposure) after turning cooling on to see at what time noise reaches a minimum. Any suggestions for other ways to test this are welcome. Thanks, Esteban This message and any attached documents are only for the use of the intended recipient(s), are confidential and may contain privileged information. Any unauthorized review, use, retransmission, or other disclosure is strictly prohibited. If you have received this message in error, please notify the sender immediately, and then delete the original message. Thank you. |
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