Oer-gcamp6f

Oer-GCaMP6f is a genetically encoded calcium indicator used in neuroscience to visualize changes in intracellular calcium associated with neuronal activity. When calcium enters an expressing neuron, it binds the indicator’s calmodulin domain and promotes interaction with the M13 peptide, altering the green fluorescent protein chromophore and increasing fluorescence; the fast variant supports rapid activity measurements. In live-cell and in vivo imaging, Oer-GCaMP6f enables researchers to monitor neural responses across individual cells, circuits, or brain regions with optical methods. These measurements help link neuronal activity to sensory processing, behavior, and circuit function while reducing the need for chemical calcium dyes.

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JoVE EoE - Neuroimaging

Spontaneous Calcium Imaging for Compartment-Specific Dynamics in Astrocytes

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2025

Source: Bannai, H., et. al., Dissection of Local Ca2+ Signals in Cultured Cells by Membrane-targeted Ca2+ Indicators. J. Vis. Exp. (2019)The video demonstrates fluorescence imaging to observe compartment-specific spontaneous calcium dynamics in astrocytes by sequentially monitoring calcium-sensitive proteins localized on the plasma membrane and endoplasmic reticulum.

In-vivo and Ex-vivo Calcium Imaging of an Olfactory Circuit Neuron in the Third-Instar Drosophila melanogaster Larva

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2025

We present calcium imaging protocols for a Drosophila larval olfactory neuron, using a topical tissue adhesive for immobilization. This method enhances stability, facilitating reliable in-vivo and ex-vivo experiments. Custom R scripts analyze calcium signals, providing an efficient platform for detailed neurophysiological research.

Infecting Primary Mouse Midbrain Neurons with Engineered Adeno-Associated Viruses

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2025

This video shows infecting primary mouse midbrain neurons with Adeno-Associated Viruses carrying a fluorescent calcium indicator. The indicator's fluorescence confirms successful infection and enables real-time monitoring of neuronal infection.

Visualization of Calcium Influx in Ventral Midbrain Neurons Derived from Mouse Embryos

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2025

Source: Bancroft, E. A., et al. Quantifying Spontaneous Ca2+ Fluxes and their Downstream Effects in Primary Mouse Midbrain Neurons. J. Vis. Exp. (2020) This video demonstrates the real-time visualization of calcium influx in ventral midbrain neurons derived from mouse embryos. Using a viral vector to express a calcium indicator, the neurons are imaged under a confocal microscope to track changes in fluorescence intensity during spontaneous and neurotransmitter-induced calcium activity.

Research

JoVE Journal - Neuroscience
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Simultaneous Photothrombosis and Fiber Photometry to Induce and Monitor Ischemic Stroke in Behaving Mice

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2025

Using an all-optical approach, ischemic stroke is induced while simultaneously recording neuronal Ca2+ activity using a fluorescent biosensor in the emerging stroke core of an awake, behaving mouse.

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