Simultaneous loose seal cell-attached recordings and two-photon imaging of GCaMP8 expressing mouse V1 neurons with drifting gratings visual stimuli
ID: 000168
DRAFT
DRAFT
Contact Rozsa, Marton
File Count 170
Size 1.3 TiB
Created November 11, 2021
Last update June 20, 2023
Licenses: spdx:CC-BY-4.0
Access Information: dandi:OpenAccess
We tested the jGCaMP8 sensors in L2/3 pyramidal neurons of mouse primary visual cortex. We made a craniotomy over V1 and infected neurons with adeno-associated virus (AAV2/1-hSynapsin-1) encoding jGCaMP8 variants (s/m/f), jGCaMP7f, or XCaMP-Gf. 18-80 days after the virus injection, the mouse was anesthetized, and we surgically removed the cranial window and performed durotomy. The craniotomy was...
Keywords:
2-photon
visual cortex
calcium
spike
action potential
layer 2
AAV
adeno-associated virus
jGCaMP8s
jGCaMP8m
jGCaMP8f
jGCaMP7f
XCaMP-Gf
Contributors
Funding information
HHMI
Related resources
Assets Summary
Approach
microscopy approach; cell population imaging
electrophysiological approach
Data StandardRRID:SCR_015242
Neurodata Without Borders (NWB)
Number Of Subjects
30
Variable Measured
PlaneSegmentation
CurrentClampStimulusSeries
CurrentClampSeries
TwoPhotonSeries
ProcessingModule
VoltageClampStimulusSeries
VoltageClampSeries
Measurement Technique
two-photon microscopy technique
current clamp technique
analytical technique
voltage clamp technique