fluorescent beads Search Results


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BIOCYTEX Inc fluorescent beads megamix-plus ssc 0.16
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abberior instruments 40-nm far-red fluorescent beads
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BIOCYTEX Inc fluorescent size-calibrated beads megamix-plus prototype
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PolyScience latex beads
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Becton Dickinson fluorescent latex counting beads becton dickinson
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Merck KGaA fluorescent beads
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AES Chemunex fluorescent yellow–green 2-lm reference beads standard g
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BioMimetic Therapeutics fluorescent beads
Schematics of ODP of 3D microvascular networks within a hydrogel fluid. (a) Hierarchical and branching networks of sacrificial ink patterned in a gel fluid. (b) Voids induced by nozzle movement are filled with liquid that migrates from the fluid capping layer. (c) Photopolymerization of supporting fluid to get crosslinked hydrogel supporting matrix. (d and e) Microvascular channels were evacuated by applying modest vacuum to liquefied ink. (f) <t>Fluorescent</t> image of a 3D microvascular network fabricated via omnidirectional printing of a sacrificial ink (dyed red) within a photopolymerized F127-diacrylate matrix. Source: Adapted with permission from Wu et al.
Fluorescent Beads, supplied by BioMimetic Therapeutics, 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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Becton Dickinson fluorescence beads calirite
Schematics of ODP of 3D microvascular networks within a hydrogel fluid. (a) Hierarchical and branching networks of sacrificial ink patterned in a gel fluid. (b) Voids induced by nozzle movement are filled with liquid that migrates from the fluid capping layer. (c) Photopolymerization of supporting fluid to get crosslinked hydrogel supporting matrix. (d and e) Microvascular channels were evacuated by applying modest vacuum to liquefied ink. (f) <t>Fluorescent</t> image of a 3D microvascular network fabricated via omnidirectional printing of a sacrificial ink (dyed red) within a photopolymerized F127-diacrylate matrix. Source: Adapted with permission from Wu et al.
Fluorescence Beads Calirite, supplied by Becton Dickinson, 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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Polysciences inc green fluorescent latex bead (flb) particles
Schematics of ODP of 3D microvascular networks within a hydrogel fluid. (a) Hierarchical and branching networks of sacrificial ink patterned in a gel fluid. (b) Voids induced by nozzle movement are filled with liquid that migrates from the fluid capping layer. (c) Photopolymerization of supporting fluid to get crosslinked hydrogel supporting matrix. (d and e) Microvascular channels were evacuated by applying modest vacuum to liquefied ink. (f) <t>Fluorescent</t> image of a 3D microvascular network fabricated via omnidirectional printing of a sacrificial ink (dyed red) within a photopolymerized F127-diacrylate matrix. Source: Adapted with permission from Wu et al.
Green Fluorescent Latex Bead (Flb) Particles, supplied by Polysciences inc, 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


Schematics of ODP of 3D microvascular networks within a hydrogel fluid. (a) Hierarchical and branching networks of sacrificial ink patterned in a gel fluid. (b) Voids induced by nozzle movement are filled with liquid that migrates from the fluid capping layer. (c) Photopolymerization of supporting fluid to get crosslinked hydrogel supporting matrix. (d and e) Microvascular channels were evacuated by applying modest vacuum to liquefied ink. (f) Fluorescent image of a 3D microvascular network fabricated via omnidirectional printing of a sacrificial ink (dyed red) within a photopolymerized F127-diacrylate matrix. Source: Adapted with permission from Wu et al.

Journal: Journal of Tissue Engineering

Article Title: Freeform 3D printing of vascularized tissues: Challenges and strategies

doi: 10.1177/20417314211057236

Figure Lengend Snippet: Schematics of ODP of 3D microvascular networks within a hydrogel fluid. (a) Hierarchical and branching networks of sacrificial ink patterned in a gel fluid. (b) Voids induced by nozzle movement are filled with liquid that migrates from the fluid capping layer. (c) Photopolymerization of supporting fluid to get crosslinked hydrogel supporting matrix. (d and e) Microvascular channels were evacuated by applying modest vacuum to liquefied ink. (f) Fluorescent image of a 3D microvascular network fabricated via omnidirectional printing of a sacrificial ink (dyed red) within a photopolymerized F127-diacrylate matrix. Source: Adapted with permission from Wu et al.

Article Snippet: Biomimetic perfusion using fluorescent beads with diameters of 2 μm (similar to platelets) was carried out and the beads were found through iterative photodegradation.

Techniques:

(a) Schematic representation of the two in vitro models (3D invasion assays and blood vessel-like structures) generated by laser-based fabrication of biomicrofluidic networks in hydrogels. (b) Assessed cell viability by live/dead staining (green: live cells, red: dead cells) with 1 h after the fabrication process (3D ctrl: conventional 3D culture on a 24-well plate, (−) μF and (+) μF: PDMS mounts without and with the fabricated network). (c) Wide-field fluorescent image of a representative, live/dead stained mouse myoblast (C 2 C 12 ) culture. (d) A representative bright-field image overlapped with the cell tracks of prestarved hMSCs perfused with PDGF-BB for 30 min. (e) Analysis of the migration distance and (f) the directionality index of hMSCs perfused with PDGF-BB for 30 min. (g) Representative bright-field image overlapped with the cell tracks of prestarved hMSCs perfused with medium only. (h) Analysis of the migration distance and (i) the directionality index of hMSCs perfused with medium only. (j) Confocal 3D reconstruction of a hollow HUVEC tube formed in collagen type I. (k) Transversal and (l) frontal plane of the structure. Frontal planes showing endothelial markers immunostainings of (m) CD-31 and (n) VE-cadherin. Source: Adapted with permission from Brandenberg and Lutolf.

Journal: Journal of Tissue Engineering

Article Title: Freeform 3D printing of vascularized tissues: Challenges and strategies

doi: 10.1177/20417314211057236

Figure Lengend Snippet: (a) Schematic representation of the two in vitro models (3D invasion assays and blood vessel-like structures) generated by laser-based fabrication of biomicrofluidic networks in hydrogels. (b) Assessed cell viability by live/dead staining (green: live cells, red: dead cells) with 1 h after the fabrication process (3D ctrl: conventional 3D culture on a 24-well plate, (−) μF and (+) μF: PDMS mounts without and with the fabricated network). (c) Wide-field fluorescent image of a representative, live/dead stained mouse myoblast (C 2 C 12 ) culture. (d) A representative bright-field image overlapped with the cell tracks of prestarved hMSCs perfused with PDGF-BB for 30 min. (e) Analysis of the migration distance and (f) the directionality index of hMSCs perfused with PDGF-BB for 30 min. (g) Representative bright-field image overlapped with the cell tracks of prestarved hMSCs perfused with medium only. (h) Analysis of the migration distance and (i) the directionality index of hMSCs perfused with medium only. (j) Confocal 3D reconstruction of a hollow HUVEC tube formed in collagen type I. (k) Transversal and (l) frontal plane of the structure. Frontal planes showing endothelial markers immunostainings of (m) CD-31 and (n) VE-cadherin. Source: Adapted with permission from Brandenberg and Lutolf.

Article Snippet: Biomimetic perfusion using fluorescent beads with diameters of 2 μm (similar to platelets) was carried out and the beads were found through iterative photodegradation.

Techniques: In Vitro, Generated, Staining, Migration