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JoVE Journal
Neuroscience

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Imaging Ca

Article doi: 10.3791/52588
May 6th, 2015 •
1,2, 1,3, 1,2,3, 4,5, 1,2,3, 1
1Institute for Ophthalmic Research, University of Tübingen, 2Graduate School of Cellular & Molecular Neuroscience, University of Tübingen, 3Bernstein Centre for Computational Neuroscience, University of Tübingen, 4Molecular Genetics Laboratory, University of Tübingen, 5Centre for Ophthalmology, University of Tübingen

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May 6th, 2015

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Wir beschreiben ein Protokoll, um Ca 2+ Dynamik in den Axonterminalen von Zapfen-Photorezeptoren mit einem ex-vivo Scheibe Vorbereitung der Maus Netzhaut zu überwachen. Dieses Protokoll ermöglicht umfassende Studien der Kegel Ca 2+ Signalisierung in einem wichtigen Säugetiermodellsystem der Maus.

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