The overall goal of bioluminescent imaging is to image in vivo functional calcium transient, a proxy for activity, for longer periods, and in deep brain structures. This method can help answer key questions in the field of neurobiology, such as wh
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Here we present a novel Ca2+-imaging approach using a bioluminescent reporter. This approach uses a fused construct GFP-aequorin which binds to Ca2+ and emits light, eliminating the need for light excitation. Significantly this method permits long continuous imaging, access to deep brain structures and high temporal resolution.