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Whole Brain Microscopy Equipment

The WBMF offers access to a unique set of high-throughput microscopes and histology resources, ideal for collecting high-content neuroscience data, for UT Southwestern and external researchers.

Please remember to acknowledge your usage of our facility resources in your publications using our established Research Resource Identifier code anywhere in your methods or acknowledgements: RRID: SCR_017949. This is critical for us to maintain support for the core.

Jump to: Light Sheet MicroscopySerial Two-Photon TomographyWhole Slide ImagingSmall Microscopes & Sectioning EquipmentComputer Workstations

Light Sheet Microscopy

SmartSPIM
LifeCanvas SmartSPIM
SmartBatch Electrophoresis image
LifeCanvas SmartBatch Electrophoresis System

Serial Two-Photon Tomography

Marinus MP
TissueVision Marinus MP
tissuecyte 1000 image
TissueVision TissueCyte 1000

Whole Slide Imaging

axioscanZ1
Zeiss AxioScan.Z1
vernino research
Zeiss Axioscan 7
nanozoomers60
Hamamatsu NanoZoomer S60

Small Microscopes and Sectioning Equipment

MZ10F
Leica MZ10F
Axioscope A1
Zeiss Axioscope.A1
vernino research
Leica VT1200 Vibrotome
CM1950
Leica CM1950 Cryostat
SM2010R
Leica SM2010R Sliding Microtome

Computer Workstations

imaris
Imaris Workstation
microbrightfield
Microbrightfield Workstation

Data Images

mouse brain slices

Equipment: Axioscan

Triple immunofluorescent staining for cell type specific markers NeuN (neurons; green), GFAP (astrocytes; red) and Iba1 (microglia; purple) in serial mouse brain sections. Nuclei are stained with DAPI and shown in blue. Sectioning, staining and whole slide scanning was performed in the Whole Brain Microscopy Facility.

Nan Yan, UTSW Dept. of Immunology.

Equipment: Axioscan 7

Mouse brain serial sections scanned on the Zeiss Axioscan 7. The sections were prepared from a mouse brain expressing tdTomato and stained with DAPI, shown in blue, to stain cell nuclei.

Teppei Fujikawa, UTSW Dept. of Internal Medicine, Center for Hypothalamic Research.

3D view of a tumor bearing whole mouse brain

Equipment: SmartSPIM lightsheet microscope

3D view of a tumor bearing whole mouse brain cleared with the Clear+ method (LifeCanvas Technologies) and imaged on the SmartSPIM lightsheet microscope. Tumor cells are visible in red and brain autofluorescence in green

Robert Bachoo, UTSW Dept. of Neurology.

Intact mouse embryo harvested at E11.5

Equipment: SmartSPIM lightsheet microscope

Intact mouse embryo harvested at E11.5 was cleared using the Clear+ method (LifeCanvas Technologies) and imaged on the LifeCanvas SmartSPIM lightsheet microscope. Red, dorsal cord neuronal population; green, tissue autofluorescence.

Images courtesy of Helen Lai, UTSW Dept. of Neuroscience and Denise Ramirez, UTSW Dept. of Neurology.

Mouse heart

Equipment: SmartSPIM lightsheet microscope

Intact mouse heart was cleared using the Clear+ method (LifeCanvas Technologies) and imaged on the LifeCanvas SmartSPIM lightsheet microscope. Red, tdTomato; green, tissue autofluorescence.

Daniel Siegwart, UTSW Dept. of Biomedical Engineering.

mouse lung

Equipment: SmartSPIM lightsheet microscope

Intact mouse lungs were cleared using the Clear+ method (LifeCanvas Technologies) and imaged on the LifeCanvas SmartSPIM lightsheet microscope. Red, tissue autofluorescence; green, GFP expression in infected cells

Chien-Ting Wu, UTSW Dept. of Microbiology.

Intact adult mouse central nervous system dorsal

Equipment: SmartSPIM lightsheet microscope

Intact adult mouse central nervous system was cleared using the Clear+ method (LifeCanvas Technologies) and imaged on the LifeCanvas SmartSPIM lightsheet microscope. Red, dorsal cord neuronal population; green, tissue autofluorescence.

Helen Lai, UTSW Dept. of Neuroscience and Denise Ramirez, UTSW Dept. of Neurology.

Intact adult mouse central nervous system lateral

Equipment: SmartSPIM lightsheet microscope

Intact adult mouse central nervous system was cleared using the Clear+ method (LifeCanvas Technologies) and imaged on the LifeCanvas SmartSPIM lightsheet microscope. Red, dorsal cord neuronal population; green, tissue autofluorescence.

Helen Lai, UTSW Dept. of Neuroscience and Denise Ramirez, UTSW Dept. of Neurology.

Segment of cleared mouse spinal cord

Equipment: SmartSPIM lightsheet microscope

Segment of cleared mouse spinal cord from dual transgenic animal expressing tdTomato in dorsal neuronal subpopulations and GFP in ventral motor neurons. Image was acquired on the LifeCanvas SmartSPIM.

Helen Lai, UTSW Dept. of Neuroscience and Denise Ramirez, UTSW Dept. of Neurology.

Whole mouse brain

Equipment: SmartSPIM lightsheet microscope

Higher resolution subvolume captured of the same brain, showing detailed neuronal and synaptic morphologies in red and green, respectively.

Wei Xu, UTSW Dept. of Neuroscience

Whole mouse brain

Equipment: SmartSPIM lightsheet microscope

Whole mouse brain was cleared using the Clear+ method (LifeCanvas Technologies) and imaged on the LifeCanvas SmartSPIM lightsheet microscope. Red, tdTomato; green, GFP; purple, tissue autofluorescence.

Wei Xu, UTSW Dept. of Neuroscience

nanozoomer-stroke

Equipment: Whole Slide Nanozoomer

Mouse brain serial sections scanned on the Hamamatsu Nanozoomer S60. The sections were prepared from a stroke model mouse and subjected to Nissl staining to visualize neuronal cell bodies and the stroke lesion area.

Mark Goldberg, UT Health San Antonio, Dept. of Neurology.

whole mouse brain

Equipment: SmartBatch

Whole mouse brain was cleared using the Clear+ method and immunostained using active staining in the LifeCanvas Smartbatch. Machine learning based tools were used to detect cFos immunostaining signal, shown in purple, which indicates neuronal activity. The cFos signal is shown overlaid onto the reference atlas in grey.

David Mangelsdorf and Steven Kliewer, UTSW Dept. of Pharmacology.

Tissuecyte: Dorsal view of raw fluorescence 3D image

Equipment: TissueCyte

Dorsal view of raw fluorescence 3D image of a double transgenic mouse brain expressing GFP and tdTomato in distinct dopamine receptor expressing populations acquired via serial two-photon tomography (STPT).

Genevieve Konopka, UTSW Dept. of Neuroscience (now at UCLA).

Dorsal view of a tumor-bearing mouse brain

Equipment: TissueCyte

Dorsal view of a segmented 3D image of a tumor-bearing mouse brain acquired via serial two-photon tomography, with tumor cells shown in blue and overlaid onto the Allen CCF 3.0 reference atlas (grey).

Sam McBrayer, UTSW Children's Research Institute.

isolated DXXr and DXXR

Equipment: TissueCyte

Dorsal view of segmented 3D images of the same brain showing isolated DXXr and DXXR expressing populations in green and red, respectively, overlaid onto the Allen CCF 3.0 reference atlas (grey).

Genevieve Konopka, UTSW Dept. of Neuroscience (now at UCLA).

songbird brain

Equipment: TissueCyte

Lateral view of a segmented 3D image of a songbird brain injected with three different neuronal tracer dyes (red, green and blue) acquired via serial two-photon tomography. Brain structural autofluorescence is shown in grey.

Todd Roberts, UTSW Dept. of Neuroscience.