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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 w/Michael that the Chroma slides are not the best for MP. I typically use an H&E stained pathology slide. This seems to be stable >3 years Rich Richard Cole Research Scientist V Director: Advanced Light Microscopy & Image Analysis Core Wadsworth Center P.O. Box 509 Albany N.Y. 12201-0509 Research Assistant Professor Dept. of Biomedical Sciences School of Public Health State University of New York Albany, New York SS518-474-7048 518-474-4430 [hidden email] Website www.wadsworth.org/cores/alm/index.htm Fluorescent plastic slides are not stabile. Depending on their exposure to light they bleach or change color. Using a pulsed laser is a good way to make little burn or other chemical reaction spots in them. Here are two old web pages with some of the problems (and benefits!) explained: http://www.einstein.yu.edu/aif/instructions/fluor-ref-slides/01.htm http://www.einstein.yu.edu/aif/instructions/zeiss/liveduo/Zaxis_bleachingtest/index.htm _______________________________________ Michael Cammer, Assistant Research Scientist Skirball Institute of Biomolecular Medicine Lab: (212) 263-3208 Cell: (914) 309-3270 ________________________________________ From: Confocal Microscopy List [[hidden email]] On Behalf Of Mark Cannell [[hidden email]] Sent: Friday, January 14, 2011 7:39 PM To: [hidden email] Subject: Re: 2P standard ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** How about Fluorescent plastic slides -I got some free from Chroma. Cheers On 15/01/2011, at 12:34 PM, Boswell, Carl A - (cboswell) wrote: > Hi all, > I'm looking for some trustworthy, permanent standard(s) to use in a MP > system to monitor the condition of detectors and the system in > general. The goal is a fluorescent source that is immutable. This > could done either by having unrestricted replacement of bleached label > with unbleached label (i.e. a solution), or a uniform and very large > solid, so that it is unlikely that any one tiny volume will be > imaged repeatedly. We've tried several iterations of an aqueous > solution of label, but sealing the prep does not prevent eventual > evaporation. Plus, there seems to be some modification of FITC, for > example, in solution over time (a month) regardless of exposure to > light. I'm not sure I can trust the consistency of colored plastic > slides, since they are not manufactured with this role in mind. One > possibility is uranyl glass slides, but Corning says they don't make > these any more. Does anyone know a source? We're also considering > quantum dots in something like immersion oil , in a sealed chamber but > I don't have any experience with these labels in a hydrophobic > environment. > > Thanks for your insights. > C > > > Carl A. Boswell, Ph.D. > Molecular and Cellular Biology > Univ. of Arizona > 520-954-7053 > FAX 520-621-3709 > IMPORTANT NOTICE: This e-mail and any attachments may contain confidential or sensitive information which is, or may be, legally privileged or otherwise protected by law from further disclosure. It is intended only for the addressee. If you received this in error or from someone who was not authorized to send it to you, please do not distribute, copy or use it or any attachments. Please notify the sender immediately by reply e-mail and delete this from your system. Thank you for your cooperation. |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Rich, what exactly are you looking at then, eosin fluorescence? Steffen On 15.01.2011 21:38, Rich Cole wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > I agree w/Michael that the Chroma slides are not the best for MP. I typically use an H&E stained pathology slide. This seems to be stable>3 years > > Rich > -- ------------------------------------------------------------ Steffen Dietzel, PD Dr. rer. nat Ludwig-Maximilians-Universität München Walter-Brendel-Zentrum für experimentelle Medizin (WBex) Head of light microscopy Mail room: Marchioninistr. 15, D-81377 München Building location: Marchioninistr. 27, München-Großhadern |
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