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krumdieck tissue slicer  (TSE systems)


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    TSE systems krumdieck tissue slicer
    Krumdieck Tissue Slicer, supplied by TSE systems, used in various techniques. Bioz Stars score: 94/100, based on 39 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tissue+slicer/Krumdieck+Tissue+Slicer/pmc12829130-51-15-18
    Average 94 stars, based on 39 article reviews
    krumdieck tissue slicer - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Primary cell culture systems to investigate host-pathogen interactions in bacterial respiratory tract infections of livestock
    Article Snippet: .. Filled lung lobes are kept on ice until the agarose becomes solid. (C) By using a tissue coring tool, cylindrical pieces of lung tissue with a bronchioles in the middle are punched out and cut into approximately 300 μm thin tissue slices by using a tissue slicer or vibratome (here: Krumdieck tissue slicer, model MD 4000-01; TSE Systems, Chesterfield, MO, USA). (D) The tissue slices are transferred to cell culture medium (e.g., RPMI) supplemented with antibiotics and antimycotics and bubbled with a normoxic gas mixture at 37°C to remove the agarose from the airway lumen. (E) PCLS can be maintained for up to two weeks in cell culture medium (e.g., RPMI) supplemented with antibiotics and antimycotics in, e.g., a 24-well plate. ..



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    Experimental design for the microdissection of equine ovarian follicles and end points evaluated. One ovary was harvested from mixed-breed mares ( n = 11) and sectioned into three ovarian portions (two lateral and one intermediary portion). The intermediary portion was further separated into three equally sized dorsal, medial, and ventral regions. The outermost cortical areas of these regions were sliced at 0.25 and 0.50 mm thicknesses using <t>a</t> <t>Stadie-Riggs</t> tissue slicer. All slices that contained visible preantral and antral follicles were subjected to microdissection to collect these follicles. The experiment was replicated 11 times, with each animal/ovary considered as one replicate. Microdissected follicles were evaluated for spatial distribution, viability, mitochondrial membrane potential, ROS, and histone trimethylation.
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    Experimental design for the microdissection of equine ovarian follicles and end points evaluated. One ovary was harvested from mixed-breed mares ( n = 11) and sectioned into three ovarian portions (two lateral and one intermediary portion). The intermediary portion was further separated into three equally sized dorsal, medial, and ventral regions. The outermost cortical areas of these regions were sliced at 0.25 and 0.50 mm thicknesses using a Stadie-Riggs tissue slicer. All slices that contained visible preantral and antral follicles were subjected to microdissection to collect these follicles. The experiment was replicated 11 times, with each animal/ovary considered as one replicate. Microdissected follicles were evaluated for spatial distribution, viability, mitochondrial membrane potential, ROS, and histone trimethylation.

    Journal: Reproduction & Fertility

    Article Title: Characterization of isolated late preantral and early antral equine ovarian follicles

    doi: 10.1530/RAF-25-0109

    Figure Lengend Snippet: Experimental design for the microdissection of equine ovarian follicles and end points evaluated. One ovary was harvested from mixed-breed mares ( n = 11) and sectioned into three ovarian portions (two lateral and one intermediary portion). The intermediary portion was further separated into three equally sized dorsal, medial, and ventral regions. The outermost cortical areas of these regions were sliced at 0.25 and 0.50 mm thicknesses using a Stadie-Riggs tissue slicer. All slices that contained visible preantral and antral follicles were subjected to microdissection to collect these follicles. The experiment was replicated 11 times, with each animal/ovary considered as one replicate. Microdissected follicles were evaluated for spatial distribution, viability, mitochondrial membrane potential, ROS, and histone trimethylation.

    Article Snippet: Each region generated four slices total: two 0.25 mm-thick slices were generated using an innovative, modified Stadie-Riggs tissue slicer (Federal University of Rio Grande; patent pending) and two 0.50 mm-thick slices were generated using a Stadie-Riggs tissue slicer (Thomas Scientific, USA).

    Techniques: Laser Capture Microdissection, Membrane