Katherina Garcia Garcia |
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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 all: We are going to buy a Multiphoton Microscope and we would like to add a laser ablation module to this system. One company offers us to do the photoablation with the same laser we do multiphoton imaging. Do you have experience doing photoablation with a multiphoton laser? Thanks in advance. Best regards, Katherina ------------------------------------------------------------------------------------------ Katherina García García Técnico de Microscopía y Citometría Tlf. 954977432 [hidden email] Centro Andaluz de Biología del Desarrollo Consejo Superior de Investigaciones Científicas Universidad Pablo Olavide Ctra. Utrera km1 41013 Sevilla España |
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 ***** On May 4, 2011, at 9:41 AM, Katherina Garcia Garcia wrote: > > We are going to buy a Multiphoton Microscope and we would like to > add a laser ablation module to this system. One company offers us to > do the photoablation with the same laser we do multiphoton imaging. > > > Do you have experience doing photoablation with a multiphoton laser? > Dear Katherine, Two few years ago, we were doing laser ablation on the actin cortex of floating and adhering fibroblasts. Jan Peychl set up an Olympus FlowView 1000, with the second scanner coupled to a 405nm PicoQuant pulsed laser (single photon ablation). We were happy with it: ablation was gentle enough for the cell to recover, and we had a large range of power for which the ablation effect could be tuned. We also tried doing ablation on the samples on Nicola Maghelli's homemade 2 photons, using the imaging infrared pulsed laser. Though our experience was very limited, we had a very hard time finding suitable parameters for the ablation to occur. Depending on the output power, we had either no effect (or bleaching), either the whole cell exploded. The parameters set for which the cortex was ablated was very sensitive, and once we have found it for one cell, it would not work for another cell. So we did not pursue in this direction, and went back to single-photon ablation. Cheers jy -- Jean-Yves Tinevez PFID - Imagopole Institut Pasteur 25-28, rue du Docteur Roux 75724 Paris cedex 15 France tel: +33 1 40 61 35 40 |
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