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acrylic mouse brain matrix  (Ted Pella)

 
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    Ted Pella acrylic mouse brain matrix
    Acrylic Mouse Brain Matrix, supplied by Ted Pella, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acrylic+mouse+brain+matrix/brain+matrix/bio_rxiv__2025__10__20__683461-41-14-18
    Average 86 stars, based on 1 article reviews
    acrylic mouse brain matrix - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    other:

    Article Title: Standardizing the mouse MCAO Stroke Model: Distinguishing Internal Carotid vs Pterygopalatine Artery Occlusion
    Article Snippet: After 24 hours mice were euthanized, the brains were extracted and placed in an acrylic mouse brain matrix (Ted Pella Inc, California, USA) and cut into coronal sections (1mm thick).



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    Illustration of tissue sectioning and embedding (A) <t>Brain</t> sectioning. (A1) Brain in a brain slicer <t>matrix.</t> Arrow shows the true lambda . (A2) Brain was cut into 1 mm slices with a brain slicer matrix and razor blades. (A3) Three coronal sections of the <t>mouse</t> brain. The second section was used for corpus callosum analysis. The line shows the edge of corpus callosum. (A4) Trimming of the brain to obtain the region of interest, corpus callosum. (A5) Enlarged picture of Figure A4. The line shows the edge of corpus callosum. (A6) Embedding mark cut at the outer edge of the corpus callosum. (B) Separated right and left optic nerves using a razor blade. (C) Spinal cord sectioning. (C1) Spinal cord was cut into 1 mm slices at the region of lumbar enlargement with a spinal cord slicer matrix and razor blades. (C2) Four coronal sections of spinal cord. (D) Immersion fixation of tissues sections in 3% glutaraldehyde at 4°C in a refrigerator overnight. (E–G) Resin embedding of the corpus callosum, optic nerve and spinal cord. Small, printed labels are included in the blocks to identify the sample. Scale bars: (A3, A4, B and C2) 0.5 cm; (A5 and A6) 0.25 cm; (E–G) 1 cm.
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    Image Search Results


    Illustration of tissue sectioning and embedding (A) Brain sectioning. (A1) Brain in a brain slicer matrix. Arrow shows the true lambda . (A2) Brain was cut into 1 mm slices with a brain slicer matrix and razor blades. (A3) Three coronal sections of the mouse brain. The second section was used for corpus callosum analysis. The line shows the edge of corpus callosum. (A4) Trimming of the brain to obtain the region of interest, corpus callosum. (A5) Enlarged picture of Figure A4. The line shows the edge of corpus callosum. (A6) Embedding mark cut at the outer edge of the corpus callosum. (B) Separated right and left optic nerves using a razor blade. (C) Spinal cord sectioning. (C1) Spinal cord was cut into 1 mm slices at the region of lumbar enlargement with a spinal cord slicer matrix and razor blades. (C2) Four coronal sections of spinal cord. (D) Immersion fixation of tissues sections in 3% glutaraldehyde at 4°C in a refrigerator overnight. (E–G) Resin embedding of the corpus callosum, optic nerve and spinal cord. Small, printed labels are included in the blocks to identify the sample. Scale bars: (A3, A4, B and C2) 0.5 cm; (A5 and A6) 0.25 cm; (E–G) 1 cm.

    Journal: STAR Protocols

    Article Title: Transmission electron microscopic analysis of myelination in the murine central nervous system

    doi: 10.1016/j.xpro.2022.101304

    Figure Lengend Snippet: Illustration of tissue sectioning and embedding (A) Brain sectioning. (A1) Brain in a brain slicer matrix. Arrow shows the true lambda . (A2) Brain was cut into 1 mm slices with a brain slicer matrix and razor blades. (A3) Three coronal sections of the mouse brain. The second section was used for corpus callosum analysis. The line shows the edge of corpus callosum. (A4) Trimming of the brain to obtain the region of interest, corpus callosum. (A5) Enlarged picture of Figure A4. The line shows the edge of corpus callosum. (A6) Embedding mark cut at the outer edge of the corpus callosum. (B) Separated right and left optic nerves using a razor blade. (C) Spinal cord sectioning. (C1) Spinal cord was cut into 1 mm slices at the region of lumbar enlargement with a spinal cord slicer matrix and razor blades. (C2) Four coronal sections of spinal cord. (D) Immersion fixation of tissues sections in 3% glutaraldehyde at 4°C in a refrigerator overnight. (E–G) Resin embedding of the corpus callosum, optic nerve and spinal cord. Small, printed labels are included in the blocks to identify the sample. Scale bars: (A3, A4, B and C2) 0.5 cm; (A5 and A6) 0.25 cm; (E–G) 1 cm.

    Article Snippet: Acrylic mouse brain matrix, coronal, 1 mm , Braintree Scientific, Inc , BS-A-5000C.

    Techniques:

    Journal: STAR Protocols

    Article Title: Transmission electron microscopic analysis of myelination in the murine central nervous system

    doi: 10.1016/j.xpro.2022.101304

    Figure Lengend Snippet:

    Article Snippet: Acrylic mouse brain matrix, coronal, 1 mm , Braintree Scientific, Inc , BS-A-5000C.

    Techniques: Recombinant, Electron Microscopy, Injection, Sterility, Software, Microscopy, Modification