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
이 콘텐츠에 액세스하려면 로그인하거나 무료 평가판을 시작하세요
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.