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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 all, To make a long story short, we have on our platform 2 Zeiss LSM 710 and 780 (NLO). They were equipped with piezo stages (Piezo Fine Focusing Stage), for specific XZ applications. As we have some issues to use them for these specific applications, we would like to have general experience feedbacks with these Zeiss piezo stages installed on scanning confocals. Particularly concerning the ease of use, re-positioning reproducibility to himself and to the z limits defined with the micro-z, lifetime of the system installed on a very used microscope… And of course we are particularly interested with any experience with Z studies, either in XYZ mode followed by orthogonal projections, or using the XZ mode! Thanks for your Help! Mag *Magali Mondin, Ph.D.* ------------------------------ *Plateforme d'imagerie PRISM* iBV – CNRS UMR 7277 – INSERM 1091 -- UNS Parc Valrose 06108 NICE cedex 2 * tel: +33 (0) 4 92 07 64 29 fax :+33 (0)4 92 07 64 32* mail : [hidden email]*; *[hidden email] ------------------------------ |
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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 Magali, Hopefully you have a resonant scanner to complement your Piezo type stage(s). R.S. enables as fast scanning in XZ as in XY. 14 full frames per second on the Leica SP5 I used to manage in Miami ... I believe the new SP8 RS is even faster, and acquiring fewer rows enables higher speed, something like 100 fps for 50 rows (the SP5 also had a rotator mirror to change scanning orientation wrt specimen). If you do not have R.S., carefully evaluate your acquisition parameters for XZ to get the performance you need. I suggest using reflection mode on a coverglass, that is, the air-coverglass-air interfaces, timelapse mode, to evaluate Z-stability (reflection gives a much brighter signal - and photostable - compared to fluorescence ... on LSM7x0's need to click a checkbox to enable bright reflection ... also, use pinhole 1 A.U.). Changing Z-range should not affect how the specimen looks. If there is a bidirectional Z option you can ask whether the surfaces are in the same pixels in each direction. Please publish what you find. It sounds like Alby can use more manuscripts for M.R.T (page charges, not gold open access without more charges). Also consider Journal of Biomolecular Techniques, http://jbt.abrf.org/ -- "gold" (immediate) open access and no publication charge and Rich Cole or Claire Brown might be the light microscopy handling editors?. Enjoy, George On 6/10/2014 3:47 AM, Magali Mondin 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 all, > > > > To make a long story short, we have on our platform 2 Zeiss LSM 710 and 780 > (NLO). They were equipped with piezo stages (Piezo Fine Focusing Stage), > for specific XZ applications. As we have some issues to use them for these > specific applications, we would like to have general experience feedbacks > with these Zeiss piezo stages installed on scanning confocals. > > > > Particularly concerning the ease of use, re-positioning reproducibility to > himself and to the z limits defined with the micro-z, lifetime of the > system installed on a very used microscope… > > > > And of course we are particularly interested with any experience with Z > studies, either in XYZ mode followed by orthogonal projections, or using > the XZ mode! > > > > Thanks for your Help! > > > > Mag > > > > *Magali Mondin, Ph.D.* > ------------------------------ > > *Plateforme d'imagerie PRISM* > iBV – CNRS UMR 7277 – INSERM 1091 -- UNS > Parc Valrose > 06108 NICE cedex 2 > > * tel: +33 (0) 4 92 07 64 29 fax :+33 (0)4 92 07 64 32* > mail : [hidden email]*; *[hidden email] > ------------------------------ > > -- George McNamara, Ph.D. Single Cells Analyst L.J.N. Cooper Lab University of Texas M.D. Anderson Cancer Center Houston, TX 77054 Tattletales http://works.bepress.com/gmcnamara/26/ |
In reply to this post by Magali Mondin
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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. ***** Magali If it is a old "very used microscope" you might want to consider having all the lubricants in the stage and focusing system cleaned and replaced with fresh lubricants to prevent slow settling or lagging that occurs due to viscosity changes in old lubricants before relying on such a sensitive translation device. Dan On Jun 10, 2014, at 4:47 AM, Magali Mondin 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 all, To make a long story short, we have on our platform 2 Zeiss LSM 710 and 780 (NLO). They were equipped with piezo stages (Piezo Fine Focusing Stage), for specific XZ applications. As we have some issues to use them for these specific applications, we would like to have general experience feedbacks with these Zeiss piezo stages installed on scanning confocals. Particularly concerning the ease of use, re-positioning reproducibility to himself and to the z limits defined with the micro-z, lifetime of the system installed on a very used microscope… And of course we are particularly interested with any experience with Z studies, either in XYZ mode followed by orthogonal projections, or using the XZ mode! Thanks for your Help! Mag *Magali Mondin, Ph.D.* ------------------------------ *Plateforme d'imagerie PRISM* iBV – CNRS UMR 7277 – INSERM 1091 -- UNS Parc Valrose 06108 NICE cedex 2 * tel: +33 (0) 4 92 07 64 29 fax :+33 (0)4 92 07 64 32* mail : [hidden email]*; *[hidden email] ------------------------------ Dan Focht Bioptechs, Inc. 3560 Beck Rd. Butler, PA 16002 www.bioptechs.com P: (724)282-7145 F: (724)282-0745 [hidden email] |
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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. ***** Thanks for your answers. More precisely, when we talk about "used" microscope it means that we have a lot of users on both systems (LSM 710 and LSM 780) and we wonder about the resistance of the stage over time ;) For our fast XZ applications (live dynamics), on both LSM 710 and LSM 780 driven by ZEN, we observe distorsions of the images when compared to XZ acquisitions done with the microscope Z. Does anyone tried these kind of acquisitions with the piezo stage mounted on either 710 or 780 microscopes? Thanks! Mag 2014-06-10 17:01 GMT+02:00 Dan Focht <[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. > ***** > > Magali > > > If it is a old "very used microscope" you might want to consider having > all the lubricants in the stage and focusing system cleaned and replaced > with fresh lubricants to prevent slow settling or lagging that occurs due > to viscosity changes in old lubricants before relying on such a sensitive > translation device. > > Dan > > > > > > On Jun 10, 2014, at 4:47 AM, Magali Mondin 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 all, > > > > To make a long story short, we have on our platform 2 Zeiss LSM 710 and 780 > (NLO). They were equipped with piezo stages (Piezo Fine Focusing Stage), > for specific XZ applications. As we have some issues to use them for these > specific applications, we would like to have general experience feedbacks > with these Zeiss piezo stages installed on scanning confocals. > > > > Particularly concerning the ease of use, re-positioning reproducibility to > himself and to the z limits defined with the micro-z, lifetime of the > system installed on a very used microscope… > > > > And of course we are particularly interested with any experience with Z > studies, either in XYZ mode followed by orthogonal projections, or using > the XZ mode! > > > > Thanks for your Help! > > > > Mag > > > > *Magali Mondin, Ph.D.* > ------------------------------ > > *Plateforme d'imagerie PRISM* > iBV – CNRS UMR 7277 – INSERM 1091 -- UNS > Parc Valrose > 06108 NICE cedex 2 > > * tel: +33 (0) 4 92 07 64 29 fax :+33 (0)4 92 07 64 32* > mail : [hidden email]*; *[hidden email] > ------------------------------ > > > Dan Focht > Bioptechs, Inc. > 3560 Beck Rd. > Butler, PA 16002 > www.bioptechs.com > P: (724)282-7145 > F: (724)282-0745 > [hidden email] > |
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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. ***** For fast xz scanning the hydraulic coupling due to the immersion fluid between the slide and objective can cause distortion especially if the slide is not well supported and/or the coverslip not well fixed to the slide. HTH Mark On 11/06/2014, at 10:43 am, Magali Mondin <[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. > ***** > > Thanks for your answers. > > More precisely, when we talk about "used" microscope it means that we have > a lot of users on both systems (LSM 710 and LSM 780) and we wonder about > the resistance of the stage over time ;) > For our fast XZ applications (live dynamics), on both LSM 710 and LSM 780 > driven by ZEN, we observe distorsions of the images when compared to XZ > acquisitions done with the microscope Z. Does anyone tried these kind of > acquisitions with the piezo stage mounted on either 710 or 780 microscopes? > > Thanks! > > Mag > > > > > 2014-06-10 17:01 GMT+02:00 Dan Focht <[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. >> ***** >> >> Magali >> >> >> If it is a old "very used microscope" you might want to consider having >> all the lubricants in the stage and focusing system cleaned and replaced >> with fresh lubricants to prevent slow settling or lagging that occurs due >> to viscosity changes in old lubricants before relying on such a sensitive >> translation device. >> >> Dan >> >> >> >> >> >> On Jun 10, 2014, at 4:47 AM, Magali Mondin 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 all, >> >> >> >> To make a long story short, we have on our platform 2 Zeiss LSM 710 and 780 >> (NLO). They were equipped with piezo stages (Piezo Fine Focusing Stage), >> for specific XZ applications. As we have some issues to use them for these >> specific applications, we would like to have general experience feedbacks >> with these Zeiss piezo stages installed on scanning confocals. >> >> >> >> Particularly concerning the ease of use, re-positioning reproducibility to >> himself and to the z limits defined with the micro-z, lifetime of the >> system installed on a very used microscope… >> >> >> >> And of course we are particularly interested with any experience with Z >> studies, either in XYZ mode followed by orthogonal projections, or using >> the XZ mode! >> >> >> >> Thanks for your Help! >> >> >> >> Mag >> >> >> >> *Magali Mondin, Ph.D.* >> ------------------------------ >> >> *Plateforme d'imagerie PRISM* >> iBV – CNRS UMR 7277 – INSERM 1091 -- UNS >> Parc Valrose >> 06108 NICE cedex 2 >> >> * tel: +33 (0) 4 92 07 64 29 fax :+33 (0)4 92 07 64 32* >> mail : [hidden email]*; *[hidden email] >> ------------------------------ >> >> >> Dan Focht >> Bioptechs, Inc. >> 3560 Beck Rd. >> Butler, PA 16002 >> www.bioptechs.com >> P: (724)282-7145 >> F: (724)282-0745 >> [hidden email] >> Mark B. Cannell Ph.D. FRSNZ Professor of Cardiac Cell Biology School of Physiology & Pharmacology Medical Sciences Building University of Bristol Bristol BS8 1TD UK [hidden email] |
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