computing densitometer with a scientific imaging system Search Results


plastic eraser  (Mitsubishi Pencil Co)
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Mitsubishi Pencil Co plastic eraser
Plastic Eraser, supplied by Mitsubishi Pencil Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/plastic eraser/product/Mitsubishi Pencil Co
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plastic eraser - by Bioz Stars, 2026-06
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5-beam nortek 1,000 khz acoustic doppler current profiler (adcp)  (Nortek Air Solutions LLC)
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Nortek Air Solutions LLC 5-beam nortek 1,000 khz acoustic doppler current profiler (adcp)
5 Beam Nortek 1,000 Khz Acoustic Doppler Current Profiler (Adcp), supplied by Nortek Air Solutions LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/5-beam nortek 1,000 khz acoustic doppler current profiler (adcp)/product/Nortek Air Solutions LLC
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two-photon benchtop microscope  (Femtonics inc)
90
Femtonics inc two-photon benchtop microscope
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
Two Photon Benchtop Microscope, supplied by Femtonics inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/two-photon benchtop microscope/product/Femtonics inc
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two-photon benchtop microscope - by Bioz Stars, 2026-06
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video digitizer image 1/at  (universal imaging inc)
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universal imaging inc video digitizer image 1/at
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
Video Digitizer Image 1/At, supplied by universal imaging inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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video digitizer image 1/at - by Bioz Stars, 2026-06
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150 illumination system  (CytoViva Inc)
90
CytoViva Inc 150 illumination system
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
150 Illumination System, supplied by CytoViva Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/150 illumination system/product/CytoViva Inc
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150 illumination system - by Bioz Stars, 2026-06
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princeton max digital camera  (universal imaging inc)
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universal imaging inc princeton max digital camera
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
Princeton Max Digital Camera, supplied by universal imaging inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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princeton max digital camera - by Bioz Stars, 2026-06
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toa probe  (Chemie GmbH)
90
Chemie GmbH toa probe
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
Toa Probe, supplied by Chemie GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/toa probe/product/Chemie GmbH
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gamma camera combined with a ct scanner gamma imager  (BIOSPACE LAB)
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BIOSPACE LAB gamma camera combined with a ct scanner gamma imager
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
Gamma Camera Combined With A Ct Scanner Gamma Imager, supplied by BIOSPACE LAB, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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gamma camera combined with a ct scanner gamma imager - by Bioz Stars, 2026-06
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spot rt 9.0 onochrome-6 camera  (MetaMorph Inc)
90
MetaMorph Inc spot rt 9.0 onochrome-6 camera
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
Spot Rt 9.0 Onochrome 6 Camera, supplied by MetaMorph Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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video-imaging system fluorcam  (Photon Systems Instruments SRO)
90
Photon Systems Instruments SRO video-imaging system fluorcam
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
Video Imaging System Fluorcam, supplied by Photon Systems Instruments SRO, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/video-imaging system fluorcam/product/Photon Systems Instruments SRO
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video-imaging system fluorcam - by Bioz Stars, 2026-06
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microcirculatory network imaging device  (MicroVision Medical)
90
MicroVision Medical microcirculatory network imaging device
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
Microcirculatory Network Imaging Device, supplied by MicroVision Medical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/microcirculatory network imaging device/product/MicroVision Medical
Average 90 stars, based on 1 article reviews
microcirculatory network imaging device - by Bioz Stars, 2026-06
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mobile mri system  (IMRIS Inc)
90
IMRIS Inc mobile mri system
A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon <t>benchtop</t> <t>microscope.</t> Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.
Mobile Mri System, supplied by IMRIS Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mobile mri system/product/IMRIS Inc
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Image Search Results


A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon benchtop microscope. Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.

Journal: bioRxiv

Article Title: All-viral tracing of monosynaptic inputs to single birthdate-defined neurons in the intact brain

doi: 10.1101/2021.10.18.464781

Figure Lengend Snippet: A) Schematic of experimental design and resulting histology 24 days after the rabies injection. Top left: a population of birthdate-matched (E14) cells in the hippocampus was targeted to express TVA and G by injecting an undiluted virus carrying Cre in utero and a large volume of the rabies helper virus carrying TVA and G in the adult hippocampus. A rabies virus carrying GCaMP6f was used to label cells providing monosynaptic input to this cell population. These inputs were then visualised via a prism implanted between the MEC (brain region marked in grey) and the cerebellum. Bottom left: confocal maximum intensity projection of the dorsal hippocampus showing cells expressing helper proteins and/or GCaMP6f. Image insets are single z-plane confocal images showing colocalization of antibody staining for a tag introduced by the helper virus and GCaMP6f introduced by the rabies virus in one example cell (i.e. a starter cell) and only GCaMP6f expression in a neighbouring cell (i.e. an input cell) highlighted with an arrow and a yellow dotted circle. Right: confocal maximum intensity projection showing input cells expressing GCaMP6f in the MEC. The white dotted line illustrates the impression made by the prism on the MEC. DG: dentate gyrus, Sub: subiculum. B) In vivo imaging example. Top left: imaging is performed with head-fixed mice under a two-photon benchtop microscope. Right: maximum intensity projection (across a 2-minute recording) of five cells in the MEC that provide monosynaptic input to the ipsilateral hippocampus 19 days after the rabies injection. Bottom left: ΔF/F traces of two cells with different activity onsets highlighted with corresponding colours in the image to the right.

Article Snippet: Mice were imaged with a custom two-photon benchtop microscope (Femtonics, Hungary) or two-photon miniscope ( Zong et al ., 2017, 2021 ; Obenhaus et al ., 2021 ).

Techniques: Injection, In Utero, Expressing, Staining, In Vivo Imaging, Imaging, Microscopy, Activity Assay