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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 friends and colleagues, For a microscope calibration assay, I am trying to image a thin layer of eGFP-like fluorophore. I aim at imaging a thin layer of fluorophore deposited on a microscopy slide. I turned to the Murray and colleague solution (1), but they image fluorescein, which spectra are quite different from eGFP. I have been looking for eGFP preparation commercially available, but unfruitfully so far. The closest I could find was the BD Living Colors EGFP Calibration Beads, but these beads are 7-10 µm in diameter, larger than the depth of focus of the systems I will use. Would you know of any solution to get or purchase eGFP on small beads? Thank you very much Best regards jyt (1) Murray et al. Evaluating performance in three-dimensional fluorescence microscopy. Journal of microscopy (2007) vol. 228 (Pt 3) pp. 390-405 -- Jean-Yves Tinevez PFID - Imagopole Institut Pasteur 25-28, rue du Docteur Roux 75724 Paris cedex 15 France tel: +33 1 40 61 31 77 |
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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 Jean-Yves, Are you talking about wide-field or confocal? If you are using WF, the intensity collected from a thin layer will depend on the depth of the layer, and one way to do measure the number of GFP molecules is to prepare a layer of GFP solution of controlled depth Cytometry Part A Volume 75A, Issue 10, pages 874–881, October 2009 Mike ________________________________________ From: Confocal Microscopy List [[hidden email]] On Behalf Of Jean-Yves Tinevez [[hidden email]] Sent: Monday, September 20, 2010 4:03 AM To: [hidden email] Subject: eGFP slides? ============================================================ To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ============================================================ Dear friends and colleagues, For a microscope calibration assay, I am trying to image a thin layer of eGFP-like fluorophore. I aim at imaging a thin layer of fluorophore deposited on a microscopy slide. I turned to the Murray and colleague solution (1), but they image fluorescein, which spectra are quite different from eGFP. I have been looking for eGFP preparation commercially available, but unfruitfully so far. The closest I could find was the BD Living Colors EGFP Calibration Beads, but these beads are 7-10 µm in diameter, larger than the depth of focus of the systems I will use. Would you know of any solution to get or purchase eGFP on small beads? Thank you very much Best regards jyt (1) Murray et al. Evaluating performance in three-dimensional fluorescence microscopy. Journal of microscopy (2007) vol. 228 (Pt 3) pp. 390-405 -- Jean-Yves Tinevez PFID - Imagopole Institut Pasteur 25-28, rue du Docteur Roux 75724 Paris cedex 15 France tel: +33 1 40 61 31 77 |
In reply to this post by Jean-Yves Tinevez-3
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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 JY, since you wrote "eGFP-like", I suppose another fluorophore with comparable excitation/emission properties will do the job? So you need a thin layer of fluorescence? One way is to use FITC in solution. You can put a drop between slide and coverslip. Or you spin-coat a coverslip with the solution, this would result in a thinner layer. FITC is very bright, but bleaching will be a problem, so maybe there are more stable dyes available in solution. Michael > ============================================================ > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ============================================================ > > Dear friends and colleagues, > > For a microscope calibration assay, I am trying to image a thin layer > of eGFP-like fluorophore. > > I aim at imaging a thin layer of fluorophore deposited on a microscopy > slide. I turned to the Murray and colleague solution (1), but they > image fluorescein, which spectra are quite different from eGFP. > > I have been looking for eGFP preparation commercially available, but > unfruitfully so far. > > The closest I could find was the BD Living Colors EGFP Calibration > Beads, but these beads are 7-10 µm in diameter, larger than the depth > of focus of the systems I will use. > > Would you know of any solution to get or purchase eGFP on small beads? > > Thank you very much > Best regards > jyt > > > > > (1) Murray et al. Evaluating performance in three-dimensional > fluorescence microscopy. Journal of microscopy (2007) vol. 228 (Pt 3) > pp. 390-405 > > > > -- > Jean-Yves Tinevez > PFID - Imagopole > Institut Pasteur > 25-28, rue du Docteur Roux > 75724 Paris cedex 15 > France > tel: +33 1 40 61 31 77 |
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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 Jean-Yves, similarly, since you wrote "eGFP-like" and "small beads", why don't you try: PS-Speck Beads from Molecular Probes, Catno P-7220 - they are subresolution beads, very bleach-resistant to my knowledge (at least for "normal" measurements...) http://products.invitrogen.com/ivgn/product/P7220?ICID=search-p7220 Just let them air-dry on your CS, embed it, and that's it... Best, Johannes Am 20.09.2010 15:54, schrieb Michael Weber: > ============================================================ > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ============================================================ > > Dear JY, > > since you wrote "eGFP-like", I suppose another fluorophore with comparable > excitation/emission properties will do the job? So you need a thin layer > of fluorescence? One way is to use FITC in solution. You can put a drop > between slide and coverslip. Or you spin-coat a coverslip with the > solution, this would result in a thinner layer. FITC is very bright, but > bleaching will be a problem, so maybe there are more stable dyes available > in solution. > > Michael > > >> ============================================================ >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ============================================================ >> >> Dear friends and colleagues, >> >> For a microscope calibration assay, I am trying to image a thin layer >> of eGFP-like fluorophore. >> >> I aim at imaging a thin layer of fluorophore deposited on a microscopy >> slide. I turned to the Murray and colleague solution (1), but they >> image fluorescein, which spectra are quite different from eGFP. >> >> I have been looking for eGFP preparation commercially available, but >> unfruitfully so far. >> >> The closest I could find was the BD Living Colors EGFP Calibration >> Beads, but these beads are 7-10 µm in diameter, larger than the depth >> of focus of the systems I will use. >> >> Would you know of any solution to get or purchase eGFP on small beads? >> >> Thank you very much >> Best regards >> jyt >> >> >> >> >> (1) Murray et al. Evaluating performance in three-dimensional >> fluorescence microscopy. Journal of microscopy (2007) vol. 228 (Pt 3) >> pp. 390-405 >> >> >> >> -- >> Jean-Yves Tinevez >> PFID - Imagopole >> Institut Pasteur >> 25-28, rue du Docteur Roux >> 75724 Paris cedex 15 >> France >> tel: +33 1 40 61 31 77 -- Mag. Johannes-P. KOCH Department of Biochemistry and Cell Biology MFPL, University of Vienna Dr. Bohrgasse 9/5 A-1030 Vienna Austria phone: 0043 1 4277 52809 fax: 0043 1 4277 9528 mail to: [hidden email] |
Boswell, Carl A - (cboswell) |
In reply to this post by Jean-Yves Tinevez-3
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ============================================================ While eGFP and FITC do have different spectra, the differences are relatively slight (~5nm difference in EM max) http://www.mcb.arizona.edu/ipc/fret/index.html, http://www.mcb.arizona.edu/IPC/spectra_page.htm. What are you hoping to do and why will FITC not work for you? Cheers, c Carl A. Boswell, Ph.D. Molecular and Cellular Biology University of Arizona 520-954-7053 FAX 520-621-3709 ----- Original Message ----- From: "Jean-Yves Tinevez" <[hidden email]> To: <[hidden email]> Sent: Monday, September 20, 2010 1:03 AM Subject: eGFP slides? ============================================================ To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ============================================================ Dear friends and colleagues, For a microscope calibration assay, I am trying to image a thin layer of eGFP-like fluorophore. I aim at imaging a thin layer of fluorophore deposited on a microscopy slide. I turned to the Murray and colleague solution (1), but they image fluorescein, which spectra are quite different from eGFP. I have been looking for eGFP preparation commercially available, but unfruitfully so far. The closest I could find was the BD Living Colors EGFP Calibration Beads, but these beads are 7-10 µm in diameter, larger than the depth of focus of the systems I will use. Would you know of any solution to get or purchase eGFP on small beads? Thank you very much Best regards jyt (1) Murray et al. Evaluating performance in three-dimensional fluorescence microscopy. Journal of microscopy (2007) vol. 228 (Pt 3) pp. 390-405 -- Jean-Yves Tinevez PFID - Imagopole Institut Pasteur 25-28, rue du Docteur Roux 75724 Paris cedex 15 France tel: +33 1 40 61 31 77 |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ============================================================ First, thank you all for the fantastic replies. On 20/09/2010 19:20, Carl Boswell wrote: > > While eGFP and FITC do have different spectra, the differences are > relatively slight (~5nm difference in EM max) > http://www.mcb.arizona.edu/ipc/fret/index.html, > http://www.mcb.arizona.edu/IPC/spectra_page.htm. What are you hoping > to do and why will FITC not work for you? Then, it is true that I am quite picky when it comes to spectra. I am trying to relate a measure made on a eGFP specimen to another measure made on a thin layer of fluorophore, ideally eGFP. Because the systems I compare have different excitation wavelength (e.g. the 470 nm of the Colibri system vs the typical 488 nm laser line), the measure made on the other fluorophore will not reflect what it would have been for eGFP... Best regards jyt |
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