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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Using Affordable LED Arrays for Photo-Stimulation of Neurons


JoVE 3379 11/15/2011

Laboratory for Perception and Memory, Institut Pasteur and Centre National de la Recherche Scientifique (CNRS)

Adult-born neurons expressing ChR2 can be manipulated in slice electrophysiological preparations in order to examine their contribution towards the function of olfactory neural circuits.

 

Specimen Preparation, Imaging, and Analysis Protocols for Knife-edge Scanning Microscopy


JoVE 3248 12/09/2011

1Department of Computer Science and Engineering, Texas A&M University, 2Beckman Institute for Advanced Science and Technology, University of Illinois, 3Department of Electrical and Computer Engineering, Kettering University, 43Scan, 5Department of Veterinary Integrative Biosciences, Texas A&M University

The full process from brain specimen preparation to serial sectioning imaging using the Knife-Edge Scanning Microscope, to data visualization and analysis is described. This technique is currently used to acquire mouse brain data, but it is applicable to other organs, other species.

 

Paired Patch Clamp Recordings from Motor-neuron and Target Skeletal Muscle in Zebrafish


JoVE 2351 11/20/2010

Vollum Institute, Oregon Health and Sciences University

Larval zebrafish represent the first vertebrate model system to allow simultaneous patch clamp recording from a spinal motor-neuron and target skeletal muscle. This video demonstrates the microscopic methods used to identify a segmental CaP motor-neuron and target muscle cells as well as the methodologies for recording from each cell type.

 

Preparation and Maintenance of Dorsal Root Ganglia Neurons in Compartmented Cultures


JoVE 951 10/17/2008

1Department of Pediatric Oncology, Dana Farber Cancer Institute, 2Department of Neurobiology, Harvard Medical School

Here we describe the technique of preparing and maintaining compartmented chambers for culturing sensory neurons of the dorsal root ganglia.

 

Isolation and Culture of Post-Natal Mouse Cerebellar Granule Neuron Progenitor Cells and Neurons


JoVE 990 1/16/2009

1Department of Genetics and Development, Columbia University , 2Department of Pathology and Cell Biology, Columbia University , 3Department of Neuroscience, Columbia University , 4Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School

Here we present a method to isolate and culture cerebellar granule neuron progenitor cells and cerebellar granule neurons from postnatal mouse.

 

High Density Event-related Potential Data Acquisition in Cognitive Neuroscience


JoVE 1945 4/16/2010

Department of Psychology, Boston College

Event-related potential (ERP) recording is under utilized in Cognitive Neuroscience because data acquisition techniques are not readily available and this method often has poor spatial resolution. To foster the increased use of ERPs in Cognitive Neuroscience, the present article details key techniques involved in high density ERP data acquisition.

 

Whole-cell Recordings of Light Evoked Excitatory Synaptic Currents in the Retinal Slice


JoVE 771 7/02/2008

1Program in Neuroscience, Boston University, 2Department of Biology, Boston University, 3Department of Biomedical Engineering, Boston University

This video shows the process of whole-cell voltage clamp recordings in the retinal slice of the aquatic tiger salamander. We demonstrate the preparation of the slice as well as how to perform patch clamp recordings during visual stimulation of the retina.

 

Primary Dissociated Midbrain Dopamine Cell Cultures from Rodent Neonates


JoVE 820 11/05/2008

Department of Pharmacology and Experimental Therapeutics, Tufts University

Primary dissociated midbrain dopamine cell cultures allow for the study of presynaptic characteristics of dopamine neurons. They can be used to monitor real-time dopamine release kinetics and protein/mRNA levels of regulators of dopamine exocytosis. Here, we show you how to generate these cultures from rodent neonates.

 

Preparation of Rat Brain Aggregate Cultures for Neuron and Glia Development Studies


JoVE 1304 9/30/2009

Department of Veterinary Integrative Biosciences, Texas A&M University (TAMU)

A protocols for an embryonic rat brain aggregate culture system is described. Multipotent progenitors in the aggregates can develop and differentiate into neurons, astrocytes and oligodendrocytes.

 

Preparation of Parasagittal Slices for the Investigation of Dorsal-ventral Organization of the Rodent Medial Entorhinal Cortex


JoVE 3802 3/28/2012

1Neuroinformatics DTC, University of Edinburgh , 2Centre for Integrative Physiology, University of Edinburgh

We describe procedures for preparation and electrophysiological recording from brain slices that maintain the dorsal-ventral axis of the medial entorhinal cortex (MEC). Because neural encoding of location follows a dorsal-ventral organization within the MEC, these procedures facilitate investigation of cellular mechanisms important for navigation and memory.

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