microvessel fragments Search Results


bz-8000 microscopic system  (KEYENCE)
90
KEYENCE bz-8000 microscopic system
Bz 8000 Microscopic System, supplied by KEYENCE, 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/product/microvessel+fragments/fluorescence+microscope+bz+9000/pmc03917243-140-24-9
Average 90 stars, based on 1 article reviews
bz-8000 microscopic system - by Bioz Stars, 2026-09
90/100 stars
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rat fat microvessel fragments rfmfs  (Dawley Inc)
86
Dawley Inc rat fat microvessel fragments rfmfs
Figure 4. Smooth muscle coverage of vessel elements changes during vascularization. Confocal image stacks of double-stained vessel elements (greenMHC and red-actin) were used to generate vessel and perivascular volumes. Single-image planes of (a) a freshly isolated <t>microvessel</t> fragment (day 0), (b) a day 8 cultured fragment, and (c) day 28 postimplantation branched vessel element. d, Percentage of vessel elements covered by -actin–positive perivascular cells measured at different time points in the model. Coverage was assessed during culturing of microvascular constructs (day 0c–day 10c) and during implanta- tion of constructs precultured for 8 days before implantation (day14i–day 28i).
Rat Fat Microvessel Fragments Rfmfs, supplied by Dawley Inc, 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/microvessel+fragments/dawley+healing+hemorrhagic+impaired+induced+model+rat+shock+sprague+vivo+wound/10__1161_slash_01__atv__0000124103__86943__1e-36-0-15
Average 86 stars, based on 1 article reviews
rat fat microvessel fragments rfmfs - by Bioz Stars, 2026-09
86/100 stars
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Image Search Results


Figure 4. Smooth muscle coverage of vessel elements changes during vascularization. Confocal image stacks of double-stained vessel elements (greenMHC and red-actin) were used to generate vessel and perivascular volumes. Single-image planes of (a) a freshly isolated microvessel fragment (day 0), (b) a day 8 cultured fragment, and (c) day 28 postimplantation branched vessel element. d, Percentage of vessel elements covered by -actin–positive perivascular cells measured at different time points in the model. Coverage was assessed during culturing of microvascular constructs (day 0c–day 10c) and during implanta- tion of constructs precultured for 8 days before implantation (day14i–day 28i).

Journal: Arteriosclerosis, Thrombosis, and Vascular Biology

Article Title: Rapid Perfusion and Network Remodeling in a Microvascular Construct After Implantation

doi: 10.1161/01.atv.0000124103.86943.1e

Figure Lengend Snippet: Figure 4. Smooth muscle coverage of vessel elements changes during vascularization. Confocal image stacks of double-stained vessel elements (greenMHC and red-actin) were used to generate vessel and perivascular volumes. Single-image planes of (a) a freshly isolated microvessel fragment (day 0), (b) a day 8 cultured fragment, and (c) day 28 postimplantation branched vessel element. d, Percentage of vessel elements covered by -actin–positive perivascular cells measured at different time points in the model. Coverage was assessed during culturing of microvascular constructs (day 0c–day 10c) and during implanta- tion of constructs precultured for 8 days before implantation (day14i–day 28i).

Article Snippet: Rat fat microvessel fragments (RFMFs) were isolated from epididymal fat pads of retired breeder male Sprague-Dawley rats.

Techniques: Staining, Isolation, Cell Culture, Construct

Figure 5. Microvascular constructs assembled from rat-derived or human-derived freshly isolated microvessel fragments (no preculturing, see Methods) also form a vascular bed on implan- tation. a, En bloc fluorescence immunostaining for all cells (anti- MHC antibody) reveals that vessels within the construct form tree-like structures. b, Ink perfusion of the host and a superficial vessel connection (arrowheads) between host and construct (arrows indicate host muscle/construct boundary). Immunostain- ing of human-derived, day 15 implants for von Willebrand factor (c) or -actin (d) indicates that vessels (arrows) are differentiated and mature. Representative sections from the same human- derived implant stained with the human-specific lectin, UEA1 labels only vessels (arrows in e) within the construct, whereas the rodent-specific vascular marker GS-1 labels vessels within only the surrounding host mouse tissue (arrows in f). The dashed lines indicate the boundary between the implant and underlying host tissue.

Journal: Arteriosclerosis, Thrombosis, and Vascular Biology

Article Title: Rapid Perfusion and Network Remodeling in a Microvascular Construct After Implantation

doi: 10.1161/01.atv.0000124103.86943.1e

Figure Lengend Snippet: Figure 5. Microvascular constructs assembled from rat-derived or human-derived freshly isolated microvessel fragments (no preculturing, see Methods) also form a vascular bed on implan- tation. a, En bloc fluorescence immunostaining for all cells (anti- MHC antibody) reveals that vessels within the construct form tree-like structures. b, Ink perfusion of the host and a superficial vessel connection (arrowheads) between host and construct (arrows indicate host muscle/construct boundary). Immunostain- ing of human-derived, day 15 implants for von Willebrand factor (c) or -actin (d) indicates that vessels (arrows) are differentiated and mature. Representative sections from the same human- derived implant stained with the human-specific lectin, UEA1 labels only vessels (arrows in e) within the construct, whereas the rodent-specific vascular marker GS-1 labels vessels within only the surrounding host mouse tissue (arrows in f). The dashed lines indicate the boundary between the implant and underlying host tissue.

Article Snippet: Rat fat microvessel fragments (RFMFs) were isolated from epididymal fat pads of retired breeder male Sprague-Dawley rats.

Techniques: Construct, Derivative Assay, Isolation, Immunostaining, Staining, Marker