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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 All, Does anyone know of, ie does it exist, a source for samples to use for training/reference on a lightsheet? Of the MuVi/Z.1/rotating variety, not diSPIMish. Kind of like using BPAE's for confocal ...? And something more exciting than beads in a plug. Thanks -- Best, Gary Laevsky, Ph.D. Director, Confocal Imaging Facility Nikon Center of Excellence Dept. of Molecular Biology Washington Rd. Princeton University Princeton, New Jersey, 08544-1014 (O) 609 258 5432 (C) 508 507 1310 |
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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. ***** We've used brine shrimp in the past. You can order them from Carolina Biological (no commercial interest). |
In reply to this post by Gary Laevsky
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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. ***** I have seen people using for that purpose a bunch of algae from the nearest garden pond, embedded in low-melting point agarose. The chloroplasts give a nice fluorescence, some of them are quite beautiful and apart from the agarose no costs are involved. Results may vary according to location and season. But in any case nature has a tendency to be more interesting than beads. Steffen Am 21.06.2018 um 14:31 schrieb Gary Laevsky: > ***** > 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 All, > > Does anyone know of, ie does it exist, a source for samples to use for > training/reference on a lightsheet? Of the MuVi/Z.1/rotating variety, not > diSPIMish. > > Kind of like using BPAE's for confocal ...? > > And something more exciting than beads in a plug. > > Thanks > ------------------------------------------------------------ Steffen Dietzel, PD Dr. rer. nat Ludwig-Maximilians-Universität München Biomedical Center (BMC) Head of the Core Facility Bioimaging Großhaderner Straße 9 D-82152 Planegg-Martinsried Germany http://www.bioimaging.bmc.med.uni-muenchen.de |
Nikos Ekizoglou - Planelight |
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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. ***** I totally agree with Steffen that a natural sample is much more interesting than beads for training. Nevertheless if you want to check the resolution of the system, especially on the z axis, you need a certified reference. Since Light Sheet is so much sample preparation related, on demos we always carry a beads sample to show the resolution of the system, independent of the samples we measure. Nikos El 21/06/2018 a las 15:06, Steffen Dietzel escribió: > ***** > 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 have seen people using for that purpose a bunch of algae from the > nearest garden pond, embedded in low-melting point agarose. The > chloroplasts give a nice fluorescence, some of them are quite > beautiful and apart from the agarose no costs are involved. Results > may vary according to location and season. But in any case nature has > a tendency to be more interesting than beads. > > Steffen > > > Am 21.06.2018 um 14:31 schrieb Gary Laevsky: >> ***** >> 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 All, >> >> Does anyone know of, ie does it exist, a source for samples to use for >> training/reference on a lightsheet? Of the MuVi/Z.1/rotating >> variety, not >> diSPIMish. >> >> Kind of like using BPAE's for confocal ...? >> >> And something more exciting than beads in a plug. >> >> Thanks >> -- *Nikos Ekizoglou* *Plane Light S.L.* Edificio CTM, O-309 28053, Madrid Tel. +34 675 966 041 /www.planelight.net / --- El software de antivirus Avast ha analizado este correo electrónico en busca de virus. https://www.avast.com/antivirus |
In reply to this post by Gary Laevsky
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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. ***** If you are looking at a 3D complex sample, and have the correct cell line you can still create some spheroids. Get some 96 well plates, coat them with poly-HEMA, put 1000 fluorescent cells in each well,, wait a couple of days to get a 400um sphere of cells, fix, pipettes them and put them in agarose. Those samples can really challenge light sheet microscopy and be a good training on optimizing imaging parameters, but not every cell line can make spheroids. 2018-06-22 8:43 GMT+01:00 Nikos Ekizoglou - PlaneLight < [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. > ***** > > I totally agree with Steffen that a natural sample is much more > interesting than beads for training. Nevertheless if you want to check the > resolution of the system, especially on the z axis, you need a certified > reference. Since Light Sheet is so much sample preparation related, on > demos we always carry a beads sample to show the resolution of the system, > independent of the samples we measure. > > Nikos > > > El 21/06/2018 a las 15:06, Steffen Dietzel escribió: > >> ***** >> 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 have seen people using for that purpose a bunch of algae from the >> nearest garden pond, embedded in low-melting point agarose. The >> chloroplasts give a nice fluorescence, some of them are quite beautiful and >> apart from the agarose no costs are involved. Results may vary according to >> location and season. But in any case nature has a tendency to be more >> interesting than beads. >> >> Steffen >> >> >> Am 21.06.2018 um 14:31 schrieb Gary Laevsky: >> >>> ***** >>> 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 All, >>> >>> Does anyone know of, ie does it exist, a source for samples to use for >>> training/reference on a lightsheet? Of the MuVi/Z.1/rotating variety, >>> not >>> diSPIMish. >>> >>> Kind of like using BPAE's for confocal ...? >>> >>> And something more exciting than beads in a plug. >>> >>> Thanks >>> >>> > -- > *Nikos Ekizoglou* > > *Plane Light S.L.* > Edificio CTM, O-309 > 28053, Madrid > Tel. +34 675 966 041 > /www.planelight.net > / > > > --- > El software de antivirus Avast ha analizado este correo electrónico en > busca de virus. > https://www.avast.com/antivirus > |
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