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Warner Product Videos on JoVE
the Journal of Visualized Experiments (JoVE)
JoVE is a novel online journal providing how-to insight by some of the best in their respective fields. While we have no official affiliation with JoVE, we recognize the value of their concept and provide the following links for the benefit of our customers.
Some links provided here are available with free access and some require a JoVE membership.
Nevertheless, we hope find the selections useful!
Dopamine Release at Individual Presynaptic Terminals Visualized with FFNs
Hui Zhang1,2, Niko G. Gubernator3,4, Minerva Yue1, Roland G. W. Staal1, Eugene V. Mosharov1, Daniela Pereira1, Vojtech Balsanek3, Paul A. Vadola3, Bipasha Mukherjee5, Robert H. Edwards5, David Sulzer12,6, Dalibor Sames3
1Departments of Neurology, Columbia University, 2Departments of Psychiatry and Pharmacology, Columbia University, 3Department of Chemistry, Columbia University, 4eMolecules, Inc., 5Departments of Neurology and Physiology, University of California School of Medicine, San Francisco, 6Division of Molecular Therapeutics, New York Psychiatric Institute
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A new means to measure neurotransmission optically using fluorescent dopamine analogs.
Related ProductsMeasuring Near Plasma Membrane and Global Intracellular Calcium Dynamics in Astrocytes
Eiji Shigetomi, Baljit S. Khakh
Departments of Physiology and Neurobiology, David Geffen School of Medicine, University of California, Los Angeles
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A new means to measure neurotransmission optically using fluorescent dopamine analogs.
Related ProductsCalcium Imaging of Cortical Neurons using Fura-2 AM
Odmara L Barreto-Chang, Ricardo E Dolmetsch
Department of Neurobiology, Stanford University
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Calcium signals play a key role in many cellular processes including gene expression, survival and differentiation. Here we demonstrate how to perform calcium imaging using Fura-2 AM. Calcium imaging is a valuable tool to study the regulation of intracellular calcium in real time and its regulation of signaling cascades.
Related ProductsBrain Slice Stimulation Using a Microfluidic Network and Standard Perfusion Chamber
Javeed Shaikh Mohammed1, Hugo Caicedo1, Christopher P. Fall2, David T. Eddington1
1Dept. of Bioengineering, University of Illinois, Chicago, 2Department of Anatomy and Cell Biology, University of Illinois, Chicago
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We demonstrate fabrication of a simple microfluidic device that can be integrated with standard electrophysiology setups to expose microscale surfaces of a brain slice in a well controlled manner to different neurotransmitters.
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