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http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal Is there any immunohistochemical marker you could suggest to use for staining neuronal cells in fixed tissue to follow up the surface of the neurons up to the level of dendritic spines for further co-staining and analysis by confocal microscopy? Thank you for your help, Tino -- Dr. Tino Jäger Department of Neurophysiology Center for Brain Research Medical University of Vienna Spitalgasse 4, A-1090 Vienna Tel: +43-1-4277-62847 Secr: +43-1-4277-62835 FAX: +43-1-4277-62865 http://www.meduniwien.ac.at |
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal Hello Tino, One of my users is "gene-gunning" DiI on 100 µm thick brain sections to stain neurons for further confocal imaging to count dendritic microspines. As he is also interested in performing immunofluorescence after imaging the spines, he is using CM DiI, wich is more resistant to permeabilization and washings than normal DiI. It took him 3-4 attempts to find the correct settings of the Gene Gun (mainly the thickness of the protective membrane), but in the end is a reasonabily easy technique. CM DiI: https://catalog.invitrogen.com/index.cfm?fuseaction=viewCatalog.viewProductD etails&productDescription=7159 Hope this helps, Xavi. ___________________________________ Xavier Sanjuan Servei de Microscòpia Confocal Departament de Ciències Experimentals i de la Salut Universitat Pompeu Fabra Parc de Recerca Biomèdica de Barcelona Doctor Aiguader, 88 - Sala 309 08003 Barcelona - Spain Tel.: + 34 93 316 08 64 Fax: + 34 93 316 09 01 E-mail: [hidden email] <mailto:[hidden email]> Web: http://www.upf.edu/cexs/sct <http://www.upf.edu/cexs/sct> -----Mensaje original----- De: Confocal Microscopy List [mailto:[hidden email]]En nombre de Tino Jäger Enviado el: dijous, 20 / març / 2008 14:43 Para: [hidden email] Asunto: Search the CONFOCAL archive at http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal Is there any immunohistochemical marker you could suggest to use for staining neuronal cells in fixed tissue to follow up the surface of the neurons up to the level of dendritic spines for further co-staining and analysis by confocal microscopy? Thank you for your help, Tino -- Dr. Tino Jäger Department of Neurophysiology Center for Brain Research Medical University of Vienna Spitalgasse 4, A-1090 Vienna Tel: +43-1-4277-62847 Secr: +43-1-4277-62835 FAX: +43-1-4277-62865 http://www.meduniwien.ac.at |
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