light-sheet microscopy Search Results


proprietary light-sheet fluorescence microscopy instruments  (Luxendo GmbH)
90
Luxendo GmbH proprietary light-sheet fluorescence microscopy instruments
Proprietary Light Sheet Fluorescence Microscopy Instruments, supplied by Luxendo GmbH, 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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light-sheet microscopy zeiss lightsheet z.1  (Carl Zeiss)
90
Carl Zeiss light-sheet microscopy zeiss lightsheet z.1
Light Sheet Microscopy Zeiss Lightsheet Z.1, supplied by Carl Zeiss, 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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lattice light sheet microscopy  (Marine Biological Laboratory)
90
Marine Biological Laboratory lattice light sheet microscopy
Lattice Light Sheet Microscopy, supplied by Marine Biological Laboratory, 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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reflective lattice light-sheet microscopy (rllsm)  (Ameta International)
90
Ameta International reflective lattice light-sheet microscopy (rllsm)
Reflective Lattice Light Sheet Microscopy (Rllsm), supplied by Ameta International, 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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z.1 light-sheet microscopy  (Carl Zeiss)
90
Carl Zeiss z.1 light-sheet microscopy
Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a <t>Z.1</t> light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.
Z.1 Light Sheet Microscopy, supplied by Carl Zeiss, 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/z.1 light-sheet microscopy/product/Carl Zeiss
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lightsheet z.1 microscopy  (Carl Zeiss)
90
Carl Zeiss lightsheet z.1 microscopy
Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a <t>Z.1</t> light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.
Lightsheet Z.1 Microscopy, supplied by Carl Zeiss, 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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open-top light-sheet microscope with 203 magnification (0.44 microns per pixel)  (Lightspeed Microscopy)
90
Lightspeed Microscopy open-top light-sheet microscope with 203 magnification (0.44 microns per pixel)
Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a <t>Z.1</t> light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.
Open Top Light Sheet Microscope With 203 Magnification (0.44 Microns Per Pixel), supplied by Lightspeed Microscopy, 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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light-sheet-based fluorescence microscopy  (Cold Spring Harbor Laboratory Meetings)
90
Cold Spring Harbor Laboratory Meetings light-sheet-based fluorescence microscopy
Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a <t>Z.1</t> light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.
Light Sheet Based Fluorescence Microscopy, supplied by Cold Spring Harbor Laboratory Meetings, 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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light-sheet-based fluorescence microscopy - by Bioz Stars, 2026-03
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lightsheet z.1 laser slice scanning microscopy system  (Carl Zeiss)
90
Carl Zeiss lightsheet z.1 laser slice scanning microscopy system
Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a <t>Z.1</t> light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.
Lightsheet Z.1 Laser Slice Scanning Microscopy System, supplied by Carl Zeiss, 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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lightsheet z.1 laser slice scanning microscopy system - by Bioz Stars, 2026-03
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light-sheet microscope running smartspim acquisition software  (LifeCanvas Technologies)
90
LifeCanvas Technologies light-sheet microscope running smartspim acquisition software
Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a <t>Z.1</t> light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.
Light Sheet Microscope Running Smartspim Acquisition Software, supplied by LifeCanvas Technologies, 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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light sheet microscopy  (Helmholtz Zentrum fur Infektionsforschung GmbH)
90
Helmholtz Zentrum fur Infektionsforschung GmbH light sheet microscopy
Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a <t>Z.1</t> light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.
Light Sheet Microscopy, supplied by Helmholtz Zentrum fur Infektionsforschung 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/light sheet microscopy/product/Helmholtz Zentrum fur Infektionsforschung GmbH
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light sheet microscopy - by Bioz Stars, 2026-03
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lightsheet microscopy lightsheet z.1  (Carl Zeiss)
90
Carl Zeiss lightsheet microscopy lightsheet z.1
Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a <t>Z.1</t> light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.
Lightsheet Microscopy Lightsheet Z.1, supplied by Carl Zeiss, 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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Image Search Results


Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a Z.1 light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.

Journal: International Journal of Molecular Sciences

Article Title: Long Preservation of AAV-Transduced Fluorescence by a Modified Organic Solvent-Based Clearing Method

doi: 10.3390/ijms23179637

Figure Lengend Snippet: Three-dimensional visualization of AAV-labeled supraspinal neurons projecting to the cervical spinal cord. ( A – C ) Lateral view of the 3D reconstruction of supraspinal neurons and tracts labeled by AAV2-Retro. A-P: anterior to posterior; D-V: dorsal to ventral. The images were acquired with a Z.1 light-sheet microscopy (Zeiss, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 0.4. ( D , E ) The magnification images of EGFP + ( D ) or mCherry + ( E ) corticospinal neurons (CSNs) in the cortex. The images were acquired with a Z.1 light-sheet microscopy equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5. ( F – I ) High-resolution confocal imaging of 2 mm thick cleared brain slices using an LSM700 equipped with a C-Apochromat 40×/1.20 water objective at a zoom of 2.0. Representative images of EGFP + ( F , H ) and mCherry + ( G , I ) are shown. a, forelimb area; b, the central population in the sensorimotor cortex; c, the corticospinal tract. D-V: dorsal to ventral; A-P: anterior to posterior. Scale bars: ( A – C ), 2 mm; ( D , E ), 50 μm; ( F , G ), 10 μm; ( H , I ), 1 μm.

Article Snippet: When samples became transparent, images were captured using Z.1 light-sheet microscopy (Z.1, Zeiss, Jena, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5 and a 20×/1.0 Plan Neofluar objective at a zoom of 1.1.

Techniques: Labeling, Microscopy, Imaging

Three-dimensional visualization of AAV-labeled supraspinal axons in the spinal cord. ( A , B ) The representative image of EGFP + and mCherry + spinal interneurons located at the corresponding injection sites. ( A’ , B’ ) The high magnification of spinal interneurons captured by LSFM. The images were acquired with a Z.1 light-sheet microscopy (Zeiss, Germany) equipped with a 20×/1.0 Plan Neofluar objective at a zoom of 1.1. ( C , D ) The EGFP + and mCherry + supraspinal axons and spinal interneurons in the cervical spinal cord rostral to the injection site. ( C’ , D’ ) The high magnification image of EGFP + and mCherry + single axons in the gray matter captured by LSFM. ( E , F ) The EGFP + and mCherry + supraspinal axons in the middle thoracic spinal cord. ( E’ , F’ ) The high magnification image of EGFP + and mCherry + single axons in the gray matter of the middle thoracic spinal cord. M-L: midline to lateral; R-C: rostral to caudal. Scale bars: ( A , B ), 200 μm; ( C – F ), 50 μm; ( A’ – F’ ), 25 μm.

Journal: International Journal of Molecular Sciences

Article Title: Long Preservation of AAV-Transduced Fluorescence by a Modified Organic Solvent-Based Clearing Method

doi: 10.3390/ijms23179637

Figure Lengend Snippet: Three-dimensional visualization of AAV-labeled supraspinal axons in the spinal cord. ( A , B ) The representative image of EGFP + and mCherry + spinal interneurons located at the corresponding injection sites. ( A’ , B’ ) The high magnification of spinal interneurons captured by LSFM. The images were acquired with a Z.1 light-sheet microscopy (Zeiss, Germany) equipped with a 20×/1.0 Plan Neofluar objective at a zoom of 1.1. ( C , D ) The EGFP + and mCherry + supraspinal axons and spinal interneurons in the cervical spinal cord rostral to the injection site. ( C’ , D’ ) The high magnification image of EGFP + and mCherry + single axons in the gray matter captured by LSFM. ( E , F ) The EGFP + and mCherry + supraspinal axons in the middle thoracic spinal cord. ( E’ , F’ ) The high magnification image of EGFP + and mCherry + single axons in the gray matter of the middle thoracic spinal cord. M-L: midline to lateral; R-C: rostral to caudal. Scale bars: ( A , B ), 200 μm; ( C – F ), 50 μm; ( A’ – F’ ), 25 μm.

Article Snippet: When samples became transparent, images were captured using Z.1 light-sheet microscopy (Z.1, Zeiss, Jena, Germany) equipped with a 5×/0.16 Plan Neofluar objective at a zoom of 2.5 and a 20×/1.0 Plan Neofluar objective at a zoom of 1.1.

Techniques: Labeling, Injection, Microscopy