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Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve Outgrowth Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve Outgrowth Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve Outgrowth Ex Vivo
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Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve Outgrowth Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve Outgrowth Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve Outgrowth Ex Vivo
1Department of Ophthalmology,Boston Children’s Hospital, 2Department of Ophthalmology,Harvard Tıp Fakültesi, 3F.M. Kirby Neurobiology Center,Boston Children’s Hospital, 4Department of Neurology,Boston Children’s Hospital, 5Department of Neurology,Harvard Tıp Fakültesi, 6Howard Hughes Medical Institute
Bölümler
- 00:04Başlık
- 00:51Pregnancy Confirmation and E10.5 Embryo Harvest and Slice Preparation
- 04:15Results: Representative Ex Vivo Oculomotor Slice Culture Development and Pitfalls
- 05:30Conclusion
Un présagéex-invivo permet d'imaginer l'excroissance du nerf oculomoteur en temps réel. Les tranches sont générées par l'intégration d'embryons E10.5 IslMN:GFP dans l'agarose, en coupant sur un vibratome et en grandissant dans un incubateur de toit de scène. Le rôle des voies de guidage d'axone est évalué en ajoutant des inhibiteurs aux médias de culture.
