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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, I found no mention of the newer ZDC 2 in the archives. I'm wondering if anyone has experience with both systems and can point out some main differences between the ZDC and PFS. How fast is the ZDC? will it maintain focus during large stage xy movements? Thanks for you help Yuval Ebenstein |
Adrian Smith-6 |
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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, I found this email in the archives but I can't see any replies. I'm also interested in any comments on:- - PFS (Nikon) vs - ZDC (Olympus) vs - ZDC 2 (Olympus) vs - UltimateFocus (API (Deltavision)) - Adaptive Focus Control (Leica) - Definite Focus (Zeiss) Did I miss anyone? :) Regards, Adrian Smith Centenary Institute, Sydney, Australia On 17/05/2011, at 5:38 AM, Yuval Ebenstein wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Hello, > I found no mention of the newer ZDC 2 in the archives. > I'm wondering if anyone has experience with both systems and can point out some main differences between the ZDC and PFS. > How fast is the ZDC? will it maintain focus during large stage xy movements? > Thanks for you help > Yuval Ebenstein |
Axel Kurt Preuss |
Dear Adrian
AFC from Leica is a marvel But it s control by metamorph is a wink wink insider approach by metamorph s engineers . ( the old game: programers make a little fun of users) But once one has captured the spirit of how MM deals with AFC and how Molecular Imaging deals with logics or ergonomics it is a marvel It is superfast and can overcome out of focus deviations (far?) above 500 um easily and in light speed. You can tip with an eppendorf against well bottom and no image disturbance. You can lift the well, same result I havent tried a sledgehammer, but probably you wont see any disturbance on the screen when it hits MM s control of AFC is typical MM, call or email me if you need further information. In particular multiwell vs slide mode has a typical programer's approach to the remote world of science Cannot comment on the other systems as i ve not tested them elaborately enough, only some of them a little. Definitely no commercial interests. Thanks Cheers Axel Sent from +6592715622 ————— Axel K Preuss, PhD, Central Imaging, IMCB, A*Star, 61 Biopolis Dr, 6-19B, Singapore 138673 [hidden email] On Jul 7, 2011, at 1:55 PM, "Adrian Smith" <[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, > > I found this email in the archives but I can't see any replies. > > I'm also interested in any comments on:- > > - PFS (Nikon) vs > - ZDC (Olympus) vs > - ZDC 2 (Olympus) vs > - UltimateFocus (API (Deltavision)) > - Adaptive Focus Control (Leica) > - Definite Focus (Zeiss) > > Did I miss anyone? :) > > Regards, > > Adrian Smith > Centenary Institute, Sydney, Australia > > > > > On 17/05/2011, at 5:38 AM, Yuval Ebenstein wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ***** >> >> Hello, >> I found no mention of the newer ZDC 2 in the archives. >> I'm wondering if anyone has experience with both systems and can point out some main differences between the ZDC and PFS. >> How fast is the ZDC? will it maintain focus during large stage xy movements? >> Thanks for you help >> Yuval Ebenstein Note: This message may contain confidential information. If this Email/Fax has been sent to you by mistake, please notify the sender and delete it immediately. Thank you. |
lechristophe |
In reply to this post by Adrian Smith-6
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I use the Zeiss Definite Focus solution. It was retrofited on our AxioObserver inverted stand, initially it was quite difficult to get it installed (had to send the stand back to Germany), but I think this was one of the first retrofited system they installed. Now they can make it on the spot easily. The system works really well, nicely integrated in Zeiss' Axiovision software (can also be driven by MM, although I didn't test it yet because I'm not willing to pay yet another MM upgrade). Sometimes I'm just surprised how perfectly horizontal the coverslip is when wandering around the coverslip looking for the next cell to image, until I realized I left the focus on "constant update"! I have no problem using it with high mag, high NA TIRF objectives. I the end I think all these systems are quite mature now, so the choice will depend more on choosing a brand for other reason (stand, software etc.), given that all these system are proprietary and will only work with a stand from the same brand. One exception is ASI's CRIFF system which can be installed on any microscope, but as it is placed on the camera port it requires to have filters that let the 780 nm laser through (as opposed to other systems which are place between the BFP of the objective and the filter cubes). Christophe On Thu, Jul 7, 2011 at 07:55, Adrian Smith <[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, > > I found this email in the archives but I can't see any replies. > > I'm also interested in any comments on:- > > - PFS (Nikon) vs > - ZDC (Olympus) vs > - ZDC 2 (Olympus) vs > - UltimateFocus (API (Deltavision)) > - Adaptive Focus Control (Leica) > - Definite Focus (Zeiss) > > Did I miss anyone? :) > > Regards, > > Adrian Smith > Centenary Institute, Sydney, Australia > > > > > On 17/05/2011, at 5:38 AM, Yuval Ebenstein wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ***** >> >> Hello, >> I found no mention of the newer ZDC 2 in the archives. >> I'm wondering if anyone has experience with both systems and can point out some main differences between the ZDC and PFS. >> How fast is the ZDC? will it maintain focus during large stage xy movements? >> Thanks for you help >> Yuval Ebenstein > |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Has anyone every constructed a DIY air table by placing a bicycle inner tube under a baseplate. It seems like a very simple and cheap solution. Would it be worthwhile to use a stack of two inner tubes and baseplates, with the inner tubes inflated to different pressures ? Any advice and alternative suggestions would be appreciated. Jeremy Adler IGP Rudbeckslaboratoriet Daghammersköljdsväg 20 751 85 Uppsala Sweden 0046 (0)18 471 4607 |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I have indeed done this, with an AFM. The baseplate was a thick slate slab. Never tried the two inner tube trick, though. It does work, though it did have additional damping above it (in the AFM enclosure) so it wasn't the sole source of isolation. We were able to get atomic resolution on a good day. This was quite a long time ago, with one of the old Park AFMs (a brilliant design for its time). Guy Optical Imaging Techniques in Cell Biology by Guy Cox CRC Press / Taylor & Francis http://www.guycox.com/optical.htm ______________________________________________ Associate Professor Guy Cox, MA, DPhil(Oxon) Australian Centre for Microscopy & Microanalysis, Madsen Building F09, University of Sydney, NSW 2006 Phone +61 2 9351 3176 Fax +61 2 9351 7682 Mobile 0413 281 861 ______________________________________________ http://www.guycox.net -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Jeremy Adler Sent: Thursday, 7 July 2011 7:23 PM To: [hidden email] Subject: Cheap Antivibration table ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Has anyone every constructed a DIY air table by placing a bicycle inner tube under a baseplate. It seems like a very simple and cheap solution. Would it be worthwhile to use a stack of two inner tubes and baseplates, with the inner tubes inflated to different pressures ? Any advice and alternative suggestions would be appreciated. Jeremy Adler IGP Rudbeckslaboratoriet Daghammersköljdsväg 20 751 85 Uppsala Sweden 0046 (0)18 471 4607 ----- No virus found in this message. Checked by AVG - www.avg.com Version: 10.0.1388 / Virus Database: 1516/3748 - Release Date: 07/06/11 |
Mario Faretta |
In reply to this post by lechristophe
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** In our lab there are two Nikon System with PFS and one Olympus ZDC2 all controlled by Metamorph. They are also compatible with the Micromanager (I tested the Olympus and it works fine) free software. The PFS, once setted the interface position, applies a continuos feedback to maintain the sample in focus with a minimal time delay being the excursion limited. If you have to acquire Z stacks it has to be disactivated and then reactivated. Control softwares allows to memorize offset positions making it very useful in "Mark and find" timelapse. The continuos focusing is also fantastic with mosaic acquisitions over large areas making the procedure very fast and precise. I think it's extremely useful and efficient. We tested it on different magnifications and numerical apertures with good results. The available objectives working with the PFS cover a wide range of nees, maybe the only limitation is that they usually have short working distance, but I am not up to date on the list of available solutions, maybe better for you to check if this is a strong limitation. The Olympus ZDC works on the same principle but essentially do not work continuously: everytime you move, the position of the interface (and consequently of the focal plane according to the offset you set) has to be recalculated moving over a range of microns (you can set it). Essentially it works similarly to the software autofocus, with the advantage of being quite fast (let's say you have a time delay of the order of 1 second according to the range you set) and not dependent on the presence of "features" in the image. I heard that Olympus is going to release a new version working in a continuous way, but it's only a rumor for me no sure info about it. Probably you already know, remember that these systems works with a defined list of objectives only and on glass (or similar optical properties) substrates (someone told me years ago that in some conditions also plastic can be tried but I have non experience on it). Hope it helps Mario Il 7/7/2011 10:26 AM, Christophe Leterrier ha scritto: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > I use the Zeiss Definite Focus solution. It was retrofited on our > AxioObserver inverted stand, initially it was quite difficult to get > it installed (had to send the stand back to Germany), but I think this > was one of the first retrofited system they installed. Now they can > make it on the spot easily. > > The system works really well, nicely integrated in Zeiss' Axiovision > software (can also be driven by MM, although I didn't test it yet > because I'm not willing to pay yet another MM upgrade). Sometimes I'm > just surprised how perfectly horizontal the coverslip is when > wandering around the coverslip looking for the next cell to image, > until I realized I left the focus on "constant update"! I have no > problem using it with high mag, high NA TIRF objectives. > > I the end I think all these systems are quite mature now, so the > choice will depend more on choosing a brand for other reason (stand, > software etc.), given that all these system are proprietary and will > only work with a stand from the same brand. One exception is ASI's > CRIFF system which can be installed on any microscope, but as it is > placed on the camera port it requires to have filters that let the 780 > nm laser through (as opposed to other systems which are place between > the BFP of the objective and the filter cubes). > > Christophe > > On Thu, Jul 7, 2011 at 07:55, Adrian Smith > <[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, >> >> I found this email in the archives but I can't see any replies. >> >> I'm also interested in any comments on:- >> >> - PFS (Nikon) vs >> - ZDC (Olympus) vs >> - ZDC 2 (Olympus) vs >> - UltimateFocus (API (Deltavision)) >> - Adaptive Focus Control (Leica) >> - Definite Focus (Zeiss) >> >> Did I miss anyone? :) >> >> Regards, >> >> Adrian Smith >> Centenary Institute, Sydney, Australia >> >> >> >> >> On 17/05/2011, at 5:38 AM, Yuval Ebenstein wrote: >> >>> ***** >>> To join, leave or search the confocal microscopy listserv, go to: >>> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >>> ***** >>> >>> Hello, >>> I found no mention of the newer ZDC 2 in the archives. >>> I'm wondering if anyone has experience with both systems and can point out some main differences between the ZDC and PFS. >>> How fast is the ZDC? will it maintain focus during large stage xy movements? >>> Thanks for you help >>> Yuval Ebenstein -- ---PLEASE Note the change in telephone number--- -- Mario Faretta Department of Experimental Oncology European Institute of Oncology c/o IFOM-IEO Campus for Oncogenomics via Adamello 16 20139 Milan Italy Phone: ++39-0294375027 email: [hidden email] http://www.ifom-ieo-campus.it |
Aryeh Weiss |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** On 7/7/11 2:51 PM, Mario Faretta wrote: > useful and efficient. We tested it on different magnifications and > numerical apertures with good results. The available objectives working > with the PFS cover a wide range of nees, maybe the only limitation is > that they usually have short working distance, but I am not up to date > on the list of available solutions, maybe better for you to check if > this is a strong limitation. I can add that we used the PFS with LWD air objectives and plastic multiwell plates, and it works well. However, if you have been using it with high NA short WD objectives, you will need to reset the offset to get it to lock. It is important that the plate not move too far out of focus when moving between wells. However, this was only a problem for us when we had a bad holder that seriously deformed the multiwell plate. --aryeh -- Aryeh Weiss School of Engineering Bar Ilan University Ramat Gan 52900 Israel Ph: 972-3-5317638 FAX: 972-3-7384051 |
In reply to this post by Guy Cox-2
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** We have done nice FCS experiments with a wide baseplate resting on a thick piece of furniture foam. It works. Sudipta On Thu, 7 Jul 2011 20:05:02 +1000, Guy Cox wrote > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > I have indeed done this, with an AFM. The baseplate was a thick > slate slab. Never tried the two inner tube trick, though. It does > work, though it did have additional damping above it (in the AFM > enclosure) so it wasn't the sole source of isolation. We were able > to get atomic resolution on a good day. This was quite a long time > ago, with one of the old Park AFMs (a brilliant design for its time). > > Guy > > Optical Imaging Techniques in Cell Biology > by Guy Cox CRC Press / Taylor & Francis > http://www.guycox.com/optical.htm > ______________________________________________ > Associate Professor Guy Cox, MA, DPhil(Oxon) > Australian Centre for Microscopy & Microanalysis, > Madsen Building F09, University of Sydney, NSW 2006 > > Phone +61 2 9351 3176 Fax +61 2 9351 7682 > Mobile 0413 281 861 > ______________________________________________ > http://www.guycox.net > > -----Original Message----- > From: Confocal Microscopy List > [mailto:[hidden email]] On Behalf Of Jeremy Adler > Sent: Thursday, 7 July 2011 7:23 PM To: [hidden email] > Subject: Cheap Antivibration table > > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Has anyone every constructed a DIY air table by placing a bicycle > inner tube under a baseplate. It seems like a very simple and cheap > solution. > > Would it be worthwhile to use a stack of two inner tubes and > baseplates, with the inner tubes inflated to different pressures ? > > Any advice and alternative suggestions would be appreciated. > > Jeremy Adler > IGP > Rudbeckslaboratoriet > Daghammersköljdsväg 20 > 751 85 Uppsala > Sweden > > 0046 (0)18 471 4607 > > ----- > No virus found in this message. > Checked by AVG - www.avg.com > Version: 10.0.1388 / Virus Database: 1516/3748 - Release Date: 07/06/11 Dr. Sudipta Maiti Associate Professor Dept. of Chemical Sciences Tata Institute of Fundamental Research Homi Bhabha Raod, Colaba, Mumbai 400005 Ph. 91-22-2278-2716 / 2539 Fax: 91-22-2280-4610 alternate e-mail: [hidden email] url: biophotonics.wetpaint.com |
Straatman, Kees (Dr.) |
In reply to this post by Aryeh Weiss
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I agree with aryeh concerning PFS and can add that the ZDC also works on multiwall plates using LWD objectives. Kees Dr Ir K.R. Straatman Senior Experimental Officer Centre for Core Biotechnology Services College of Medicine, Biological Sciences and Psychology http://www.le.ac.uk/biochem/microscopy/home.html -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Aryeh Weiss Sent: 07 July 2011 13:22 To: [hidden email] Subject: Re: Focus mechanisms... Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** On 7/7/11 2:51 PM, Mario Faretta wrote: > useful and efficient. We tested it on different magnifications and > numerical apertures with good results. The available objectives working > with the PFS cover a wide range of nees, maybe the only limitation is > that they usually have short working distance, but I am not up to date > on the list of available solutions, maybe better for you to check if > this is a strong limitation. I can add that we used the PFS with LWD air objectives and plastic multiwell plates, and it works well. However, if you have been using it with high NA short WD objectives, you will need to reset the offset to get it to lock. It is important that the plate not move too far out of focus when moving between wells. However, this was only a problem for us when we had a bad holder that seriously deformed the multiwell plate. --aryeh -- Aryeh Weiss School of Engineering Bar Ilan University Ramat Gan 52900 Israel Ph: 972-3-5317638 FAX: 972-3-7384051 |
Watkins, Simon C |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** With all these devices you need to make sure that the blocking glass in the system does not confound your experiments. for example if you work in the near IR (Cy5-7) or near UV (Fura) you should check the light transmission for the chosen device to ensure compatibility. S Simon C. Watkins Ph.D, FRC Path Professor and Vice Chair Cell Biology and Physiology Professor Immunology Director Center for Biologic Imaging BSTS 225 University of Pittsburgh 3500 Terrace St Pittsburgh PA 15261 412-352-2277 www.cbi.pitt.edu -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Straatman, Kees R. (Dr.) Sent: Thursday, July 07, 2011 8:38 AM To: [hidden email] Subject: Re: Focus mechanisms... Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I agree with aryeh concerning PFS and can add that the ZDC also works on multiwall plates using LWD objectives. Kees Dr Ir K.R. Straatman Senior Experimental Officer Centre for Core Biotechnology Services College of Medicine, Biological Sciences and Psychology http://www.le.ac.uk/biochem/microscopy/home.html -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Aryeh Weiss Sent: 07 July 2011 13:22 To: [hidden email] Subject: Re: Focus mechanisms... Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** On 7/7/11 2:51 PM, Mario Faretta wrote: > useful and efficient. We tested it on different magnifications and > numerical apertures with good results. The available objectives working > with the PFS cover a wide range of nees, maybe the only limitation is > that they usually have short working distance, but I am not up to date > on the list of available solutions, maybe better for you to check if > this is a strong limitation. I can add that we used the PFS with LWD air objectives and plastic multiwell plates, and it works well. However, if you have been using it with high NA short WD objectives, you will need to reset the offset to get it to lock. It is important that the plate not move too far out of focus when moving between wells. However, this was only a problem for us when we had a bad holder that seriously deformed the multiwell plate. --aryeh -- Aryeh Weiss School of Engineering Bar Ilan University Ramat Gan 52900 Israel Ph: 972-3-5317638 FAX: 972-3-7384051 |
Massimiliano Garre' |
In reply to this post by Jeremy Adler-4
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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 Jeremy, as both imaging facilty technician and turntable fanatic I can say that air based anti-vibration solutions are among ther best solutions in case of low budget DIY projects. As a suggestion I would use 3 small tubes (like those ones used in kids bikes) rather than 1 large, so that it would be simpler to adjust the planarity of the system Moreover you could improve the result by placing everything on top of a vibrations killing base that you could build yourself, like this one: http://www.tnt-audio.com/clinica/sandblaster_e.html both sand and talc powder are cheap and impressive in stopping unwanted vibrations, but you will have to pay particular attention in protecting your instrument from the contact with the material used. My two cents Max Garre' |
In reply to this post by Jeremy Adler-4
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Back at UCL, we manufactured our own 'anti-vibration' microscope tables we used Fabreeka anti-vibration rubber pads [square air indents in a thick rubber sheet] rather than squash balls or a bicycle inner tube as others have found when you get a puncture or a squash ball finally pops its a pain diss-assembling it all - Fabcel pads never need pumping up and retain their shape under load [a flat sheet]. I added a very heavily weighted slab on the top of the pads - I was hoping for granite but the cost [from a kitchen worktop supplier] was quite high including delivery in London so our workshop made a large and very heavy [something like 21" x 18" x 1"] slab of machined steel which they covered with black Fablon [sticky back plastic] to make it look a bit less naff. The steel slab did ring like a bell when hit with anything metal [not good] but it's shear mass, coupled with the Fabcel pads, actually worked quite well [i.e. the vibrational energy couldn't bounce a slab of that weight up and down much]. Quite importantly we had the absolutely rubbish bench worktop underneath the microscopes re-inforced with extra legs so that it no longer wobbled when you tapped on it. Fabcel pads http://docs-europe.electrocomponents.com/webdocs/0030/0900766b80030073.pdf http://uk.rs-online.com/web/p/anti-vibration-mounts/3660150 The fabcel pads were a bit weird [ours were all coated with like a sticky silicon - but at least no surface dust problems]. Fabreeka do mentioned using Fabcel pads for 'microscopes' [Fabcel 25 recommended, although I think we used the thicker Fabcel 50 variety as our metal slab was heavy - I can check that]. We cut them into smaller squares as ours were the 18"x18" pads [to about 4" square from memory, four near the outside corners, tucked in out of view, and one in the middle] and we put 2 pads thickness under the slab, which worked well. It all cost about £600 including workshop time and the £80 reinforcement under-bench box-steel legs+feet [would have been twice that with our granite supplier] - most of that cost was the machined mild steel slab. We stuck a thin ribbed rubber mat material onto the top of Fablon coated slab to give a tougher top surface for the microscope to rest on. From memory We used the lighter load Fabcel 50 pads and stuck the two 4"x 4"ish square pads together by double sided tape after trying to remove a bit of the Fabcel's sticky 'silicon' coating. You might be able to get machined granite/marble or black slate slabs cheaper than I could - and some use cheap concrete slabs but I thought that bit tacky and dust prone. Anyway it worked for us - tapping the worktop next to the microscope no longer 'wobbled' the field in view and the door slamming in the corridor outside no longer caused similar problems. Our two microscopes [Zeiss Axiovert 100's with 10x air to 63x oil objectives] were on the 4th floor by a busy London road. All our other microscopes came expensive with air tables [confocals] or similar manufacturer supplied damping plates [Zeiss/PALM]. Regards Keith --------------------------------------------------------------------------- Dr Keith J. Morris, Molecular Cytogenetics and Microscopy Core, Laboratory 00/069 and 00/070, The Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Oxford OX3 7BN, United Kingdom. Telephone: +44 (0)1865 287568 Email: [hidden email] Web-pages: http://www.well.ox.ac.uk/molecular-cytogenetics-and-microscopy -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Jeremy Adler Sent: 07 July 2011 10:23 To: [hidden email] Subject: Cheap Antivibration table ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Has anyone every constructed a DIY air table by placing a bicycle inner tube under a baseplate. It seems like a very simple and cheap solution. Would it be worthwhile to use a stack of two inner tubes and baseplates, with the inner tubes inflated to different pressures ? Any advice and alternative suggestions would be appreciated. Jeremy Adler IGP Rudbeckslaboratoriet Daghammersköljdsväg 20 751 85 Uppsala Sweden 0046 (0)18 471 4607 |
In reply to this post by Jeremy Adler-4
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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 List, There are some ideas in the Holography Handbook http://search.barnesandnoble.com/Holography-Handbook/Fred-Unterseher/e/9780894960161 Thank you for your time, and Best Regards, R. Eric King OEM & International Sales Manager [hidden email] www.LaserInnovations.com LASER INNOVATIONS 1150 East Main Street Santa Paula, CA 93060 (805) 933-0015 (805) 933-0042 fax www.CoherentLaser.com www.244nm.com www.337nm.com www.355nm.com www.488nm.com www.532nm.com www.Solidimaging.com Confidentiality Notice: This message and any documents attached hereto will be considered confidential and the actual receipt of this correspondence alone acknowledges acceptance of Non-Disclosure which in itself contains information copy righted and/or protected by Laser Innovations. They are intended for the sole use of the intended recipient. Any review, reliance or distribution by others or forwarding without express written permission is strictly prohibited. If you have received this transmission in error, please contact the sender and delete all copies. ----- Original Message ----- From: "Jeremy Adler" <[hidden email]> To: <[hidden email]> Sent: Thursday, July 07, 2011 2:22 AM Subject: Cheap Antivibration table > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Has anyone every constructed a DIY air table by placing a bicycle > inner tube under a baseplate. It seems like a very simple and cheap > solution. > > Would it be worthwhile to use a stack of two inner tubes and > baseplates, with the inner tubes inflated to different pressures ? > > Any advice and alternative suggestions would be appreciated. > > > Jeremy Adler > IGP > Rudbeckslaboratoriet > Daghammersköljdsväg 20 > 751 85 Uppsala > Sweden > > 0046 (0)18 471 4607 > |
In reply to this post by Keith Morris
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Slate makes a good top and you can often get a cheap slab by going to a billiard table manufacturer and getting a reject piece. (A table has 3 pieces which are carefully matched, so if one gets chipped or broken the other two are going begging). It has a beautifully smooth surface and needs no covering. The slow-combustion wood stove which heats the room where I'm writing this stands on just such a piece. (No, I'm not in the university right now!) Guy Optical Imaging Techniques in Cell Biology by Guy Cox CRC Press / Taylor & Francis http://www.guycox.com/optical.htm ______________________________________________ Associate Professor Guy Cox, MA, DPhil(Oxon) Australian Centre for Microscopy & Microanalysis, Madsen Building F09, University of Sydney, NSW 2006 Phone +61 2 9351 3176 Fax +61 2 9351 7682 Mobile 0413 281 861 ______________________________________________ http://www.guycox.net -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Keith Morris Sent: Thursday, 7 July 2011 11:48 PM To: [hidden email] Subject: Re: Cheap Antivibration table ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Back at UCL, we manufactured our own 'anti-vibration' microscope tables we used Fabreeka anti-vibration rubber pads [square air indents in a thick rubber sheet] rather than squash balls or a bicycle inner tube as others have found when you get a puncture or a squash ball finally pops it's a pain diss-assembling it all - Fabcel pads never need pumping up and retain their shape under load [a flat sheet]. I added a very heavily weighted slab on the top of the pads - I was hoping for granite but the cost [from a kitchen worktop supplier] was quite high including delivery in London so our workshop made a large and very heavy [something like 21" x 18" x 1"] slab of machined steel which they covered with black Fablon [sticky back plastic] to make it look a bit less naff. The steel slab did ring like a bell when hit with anything metal [not good] but it's shear mass, coupled with the Fabcel pads, actually worked quite well [i.e. the vibrational energy couldn't bounce a slab of that weight up and down much]. Quite importantly we had the absolutely rubbish bench worktop underneath the microscopes re-inforced with extra legs so that it no longer wobbled when you tapped on it. Fabcel pads http://docs-europe.electrocomponents.com/webdocs/0030/0900766b80030073.pdf http://uk.rs-online.com/web/p/anti-vibration-mounts/3660150 The fabcel pads were a bit weird [ours were all coated with like a sticky silicon - but at least no surface dust problems]. Fabreeka do mentioned using Fabcel pads for 'microscopes' [Fabcel 25 recommended, although I think we used the thicker Fabcel 50 variety as our metal slab was heavy - I can check that]. We cut them into smaller squares as ours were the 18"x18" pads [to about 4" square from memory, four near the outside corners, tucked in out of view, and one in the middle] and we put 2 pads thickness under the slab, which worked well. It all cost about £600 including workshop time and the £80 reinforcement under-bench box-steel legs+feet [would have been twice that with our granite supplier] - most of that cost was the machined mild steel slab. We stuck a thin ribbed rubber mat material onto the top of Fablon coated slab to give a tougher top surface for the microscope to rest on. From memory We used the lighter load Fabcel 50 pads and stuck the two 4"x 4"ish square pads together by double sided tape after trying to remove a bit of the Fabcel's sticky 'silicon' coating. You might be able to get machined granite/marble or black slate slabs cheaper than I could - and some use cheap concrete slabs but I thought that bit tacky and dust prone. Anyway it worked for us - tapping the worktop next to the microscope no longer 'wobbled' the field in view and the door slamming in the corridor outside no longer caused similar problems. Our two microscopes [Zeiss Axiovert 100's with 10x air to 63x oil objectives] were on the 4th floor by a busy London road. All our other microscopes came expensive with air tables [confocals] or similar manufacturer supplied damping plates [Zeiss/PALM]. Regards Keith --------------------------------------------------------------------------- Dr Keith J. Morris, Molecular Cytogenetics and Microscopy Core, Laboratory 00/069 and 00/070, The Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Oxford OX3 7BN, United Kingdom. Telephone: +44 (0)1865 287568 Email: [hidden email] Web-pages: http://www.well.ox.ac.uk/molecular-cytogenetics-and-microscopy -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Jeremy Adler Sent: 07 July 2011 10:23 To: [hidden email] Subject: Cheap Antivibration table ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Has anyone every constructed a DIY air table by placing a bicycle inner tube under a baseplate. It seems like a very simple and cheap solution. Would it be worthwhile to use a stack of two inner tubes and baseplates, with the inner tubes inflated to different pressures ? Any advice and alternative suggestions would be appreciated. Jeremy Adler IGP Rudbeckslaboratoriet Daghammersköljdsväg 20 751 85 Uppsala Sweden 0046 (0)18 471 4607 ----- No virus found in this message. Checked by AVG - www.avg.com Version: 10.0.1388 / Virus Database: 1516/3748 - Release Date: 07/06/11 |
Gareth Howell |
In reply to this post by Yuval Ebenstein
Hi, on a related note: We are currently planning to put together a live cell imaging station controlled through Metamorph software. We were thinking of utilising the MM autofocus capability (of which I have no experience) so I was wondering what you guys thought of it compared to say splashing out a little more and getting something along the lines of PFS and ZDC on a new stand?
Thanks Gareth |
Axel Kurt Preuss |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Gareth The Metamorph software AF is OK but not perfect crisp. It helps if you want to image thicker plastic plates. Leica continuous focus needs glass or very thin plastic well bottoms. Leica s continuous focus is much faster than Olympus. I haven't looked at Nikon s PFS but my users normally tend to switch it off. Olympus AF needs also to be within a relatively narrow range Hope that helps Axel -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Gareth Howell Sent: Friday, 8 July, 2011 6:26 PM To: [hidden email] Subject: Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi, on a related note: We are currently planning to put together a live cell imaging station controlled through Metamorph software. We were thinking of utilising the MM autofocus capability (of which I have no experience) so I was wondering what you guys thought of it compared to say splashing out a little more and getting something along the lines of PFS and ZDC on a new stand? Thanks Gareth -- View this message in context: http://confocal-microscopy-list.588098.n2.nabble.com/Olympus-ZDC-2-vs-Nikon-PFS-tp6370076p6562023.html Sent from the Confocal Microscopy List mailing list archive at Nabble.com. Note: This message may contain confidential information. If this Email/Fax has been sent to you by mistake, please notify the sender and delete it immediately. Thank you. |
robert.dunakin |
In reply to this post by Yuval Ebenstein
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** ----- Original Message ----- From: Axel Kurt Preuss [[hidden email]] Sent: 07/08/2011 06:58 PM ZE8 To: [hidden email] Subject: Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Gareth The Metamorph software AF is OK but not perfect crisp. It helps if you want to image thicker plastic plates. Leica continuous focus needs glass or very thin plastic well bottoms. Leica s continuous focus is much faster than Olympus. I haven't looked at Nikon s PFS but my users normally tend to switch it off. Olympus AF needs also to be within a relatively narrow range Hope that helps Axel -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Gareth Howell Sent: Friday, 8 July, 2011 6:26 PM To: [hidden email] Subject: Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi, on a related note: We are currently planning to put together a live cell imaging station controlled through Metamorph software. We were thinking of utilising the MM autofocus capability (of which I have no experience) so I was wondering what you guys thought of it compared to say splashing out a little more and getting something along the lines of PFS and ZDC on a new stand? Thanks Gareth -- View this message in context: http://confocal-microscopy-list.588098.n2.nabble.com/Olympus-ZDC-2-vs-Nikon-PFS-tp6370076p6562023.html Sent from the Confocal Microscopy List mailing list archive at Nabble.com. Note: This message may contain confidential information. If this Email/Fax has been sent to you by mistake, please notify the sender and delete it immediately. Thank you. ______________________________________________________________________ This email has been scanned by the MessageLabs Email Security System. For more information please visit http://www.messagelabs.com/email ______________________________________________________________________ |
robert.dunakin |
In reply to this post by Yuval Ebenstein
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Eé ----- Original Message ----- From: Axel Kurt Preuss [[hidden email]] Sent: 07/08/2011 06:58 PM ZE8 To: [hidden email] Subject: Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Gareth The Metamorph software AF is OK but not perfect crisp. It helps if you want to image thicker plastic plates. Leica continuous focus needs glass or very thin plastic well bottoms. Leica s continuous focus is much faster than Olympus. I haven't looked at Nikon s PFS but my users normally tend to switch it off. Olympus AF needs also to be within a relatively narrow range Hope that helps Axel -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Gareth Howell Sent: Friday, 8 July, 2011 6:26 PM To: [hidden email] Subject: Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi, on a related note: We are currently planning to put together a live cell imaging station controlled through Metamorph software. We were thinking of utilising the MM autofocus capability (of which I have no experience) so I was wondering what you guys thought of it compared to say splashing out a little more and getting something along the lines of PFS and ZDC on a new stand? Thanks Gareth -- View this message in context: http://confocal-microscopy-list.588098.n2.nabble.com/Olympus-ZDC-2-vs-Nikon-PFS-tp6370076p6562023.html Sent from the Confocal Microscopy List mailing list archive at Nabble.com. Note: This message may contain confidential information. If this Email/Fax has been sent to you by mistake, please notify the sender and delete it immediately. Thank you. ______________________________________________________________________ This email has been scanned by the MessageLabs Email Security System. For more information please visit http://www.messagelabs.com/email ______________________________________________________________________ |
Cameron Nowell |
In reply to this post by Axel Kurt Preuss
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Howdy, We use the MetaMorph autofocus quite often. If you tweak it right (binning, range fr searching etc.) it can be quite fast. Also the advantage of any image based atofocus system is that it will compensate for your sample moving up or down, or flattening out, over time. Systems like the Olympus ZDC (which we use on our confocal system), Nikon PF etc all find the coverslip again. If you sample doesn't move in the same way as the cover slip you may have issues with the focus drifting anyway. Of the three laser based focus systems i think Nions is the fastests, Olypus the slowest and Leica in between. All can be a bit of a pain to set up though. Cheers Cam Cameron J. Nowell Microscpy Manager Central Resource for Advanced Microscopy Ludwig Insttue for Cancer Research PO Box 2008 Royal Melbourne Hospital Victoria, 3050 AUSTRALIA Office: +61 3 9341 3155 Mobile: +61422882700 Fax: +61 3 9341 3104 http://www.ludwig.edu.au/branch/research/platform/microscopy.htm ________________________________ From: Confocal Microscopy List on behalf of Axel Kurt Preuss Sent: Fri 7/8/2011 8:58 PM To: [hidden email] Subject: Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Gareth The Metamorph software AF is OK but not perfect crisp. It helps if you want to image thicker plastic plates. Leica continuous focus needs glass or very thin plastic well bottoms. Leica s continuous focus is much faster than Olympus. I haven't looked at Nikon s PFS but my users normally tend to switch it off. Olympus AF needs also to be within a relatively narrow range Hope that helps Axel -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Gareth Howell Sent: Friday, 8 July, 2011 6:26 PM To: [hidden email] Subject: Re: Olympus ZDC 2 vs. Nikon PFS ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi, on a related note: We are currently planning to put together a live cell imaging station controlled through Metamorph software. We were thinking of utilising the MM autofocus capability (of which I have no experience) so I was wondering what you guys thought of it compared to say splashing out a little more and getting something along the lines of PFS and ZDC on a new stand? Thanks Gareth -- View this message in context: http://confocal-microscopy-list.588098.n2.nabble.com/Olympus-ZDC-2-vs-Nikon-PFS-tp6370076p6562023.html Sent from the Confocal Microscopy List mailing list archive at Nabble.com. Note: This message may contain confidential information. If this Email/Fax has been sent to you by mistake, please notify the sender and delete it immediately. Thank you. |
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