The Journal of Visualized Experiments (JoVE) is a peer reviewed, PubMed-indexed video journal. Our mission is to increase the productivity of scientific research.

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How to Create and Use Binocular Rivalry


JoVE 2030 11/10/2010

1Department of Psychology, New York University, 2Centre for Neural Science, New York University, 3Department of Psychology, Princeton University, 4Neuroscience Institute, Princeton University

Binocular rivalry occurs when the eyes are presented with different images at the same location: one image dominates while the other is suppressed, and dominance alternates periodically. Rivalry is useful for investigating perceptual selection and visual awareness. Here we describe several easy methods for creating and using binocular rivalry stimuli.

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Axoplasm Isolation from Rat Sciatic Nerve


JoVE 2087 9/24/2010

Department of Biological Chemistry, Weizmann Institute of Science

We demonstrate a protocol for axoplasm isolation from adult rat sciatic nerve based on dissection of nerve fascicles and incubation in hypotonic medium to release myelin and lyse non-axonal structures, followed by extraction of the remaining axon-enriched material.

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In vivo Imaging of Intact Drosophila Larvae at Sub-cellular Resolution


JoVE 2249 9/10/2010

1Junior Research Group Synaptic Plasticity, Hertie Institute for Clinical Brain Research, University of Tübingen, 2Graduate School of Cellular and Molecular Neuroscience, University of Tübingen

This protocol describes a reliable method for anesthetization and imaging of intact Drosophila melanogaster larvae. We have utilized the volatile anesthetic desflurane to allow for repetitive imaging at sub-cellular resolution and re-identification of structures for up to a few days1.

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Dissection of a Mouse Eye for a Whole Mount of the Retinal Pigment Epithelium


JoVE 2563 2/27/2011

UT Health Science Center at San Antonio, Greehey Children's Cancer Research Institute and Department of Cellular and Structural Biology

A formal demonstration of the dissection of a mouse eye, resulting in a whole mount of the retinal pigment epithelium.

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Methods for Rapid Transfer and Localization of Lyme Disease Pathogens Within the Tick Gut


JoVE 2544 2/14/2011

1Department of Veterinary Medicine, University of Maryland, 2Department of Entomology, Connecticut Agricultural Experiment Station

Lyme disease research studies often require generation of ticks infected with the pathogen Borrelia burgdorferi, a process that typically takes several weeks. Here we demonstrate a microinjection-based tick infection procedure that can be accomplished within hours. We also demonstrate an immunofluorescence method for in situ localization of B. burgdorferi within ticks.

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Mechanical Manipulation of Neurons to Control Axonal Development


JoVE 2509 4/10/2011

Department of Zoology, Michigan State University, East Lansing

Application and direct measurements of forces on neurons in the 2-1000 microdyne range are achieved with high precision using calibrated glass needles. This methodology can be used to control and measure several aspects of axonal development, including axonal initiation, axonal tension, velocity of axonal elongation, and force vectors.

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Using a Comparative Species Approach to Investigate the Neurobiology of Paternal Responses


JoVE 3173 9/19/2011

1Department of Psychology, Randolph-Macon College, 2Department of Psychology, Marshall University

The comparative species approach allows behavioral neuroscientists to explore various neurobiological factors associated with specific behaviors viewed as characteristic of a specific animal model. Taking advantage of naturally occurring differences in behavior between closely related species, this technique doesn’t require invasive techniques to manipulate the expression of the behavior.

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An Experimental Platform to Study the Closed-loop Performance of Brain-machine Interfaces


JoVE 1677 3/10/2011

Department of Bioengineering, Imperial College London

We use a closed-loop fly-machine interface to investigate general principles in neuronal control.

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Paraffin-Embedded and Frozen Sections of Drosophila Adult Muscles


JoVE 2438 12/27/2010

Gene Expression and Signaling Research Group, Max Planck Institute for Biophysical Chemistry

Identification of mechanisms underlying muscle damage is crucial. Here we present the histological technique for preparing paraffin-embedded and frozen sections of Drosophila thoracic muscles. This allows analysis of muscle morphology and localization of protein and other muscle cell components.

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A Functional Motor Unit in the Culture Dish: Co-culture of Spinal Cord Explants and Muscle Cells


JoVE 3616 4/12/2012

Biozentrum, University of Basel

Cultured muscle cells are an inadequate model to recapitulate innervated muscle in vivo. A functional motor unit can be reproduced in vitro by innervation of differentiated human primary muscle cells using rat embryo spinal cord explants. This article describes how co-cultures of spinal cord explants and muscle cells are established.

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