computer program scaffold version 4.6 Search Results


3d discovery printer  (RegenHU Ltd)
90
RegenHU Ltd 3d discovery printer
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
3d Discovery Printer, supplied by RegenHU Ltd, 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/computer+program+scaffold+version+4%2E6/3d+discovery+bioprinter/pmc09668579-93-7-12
Average 90 stars, based on 1 article reviews
3d discovery printer - by Bioz Stars, 2026-09
90/100 stars
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scaffold version scaffold72703701  (Proteome Software Inc)
86
Proteome Software Inc scaffold version scaffold72703701
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Scaffold Version Scaffold72703701, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/proteome+scaffold72703701/cipriano_michael_joseph__2013__an_analysis_of_kinetochore_proteins_in_a_wide_range_of_eukaryotes_and_the_kinetochore_of_giardia-924-3-4
Average 86 stars, based on 1 article reviews
scaffold version scaffold72703701 - by Bioz Stars, 2026-09
86/100 stars
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scaffold v 4  (Proteome Software Inc)
86
Proteome Software Inc scaffold v 4
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Scaffold V 4, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/q+s+scaffold/pm34707224-366-6-9
Average 86 stars, based on 1 article reviews
scaffold v 4 - by Bioz Stars, 2026-09
86/100 stars
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scaffold quant v5 0 3 softwares  (Proteome Software Inc)
86
Proteome Software Inc scaffold quant v5 0 3 softwares
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Scaffold Quant V5 0 3 Softwares, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/0+3+quant+scaffold+softwares+v5/pm41518903-104-19-23
Average 86 stars, based on 1 article reviews
scaffold quant v5 0 3 softwares - by Bioz Stars, 2026-09
86/100 stars
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scaffold 5 0 1 software  (Proteome Software Inc)
86
Proteome Software Inc scaffold 5 0 1 software
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Scaffold 5 0 1 Software, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/scaffold/10__1007_slash_s11947___023___03222___x-179-4-7
Average 86 stars, based on 1 article reviews
scaffold 5 0 1 software - by Bioz Stars, 2026-09
86/100 stars
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scaffold dia v 2 0 0  (Proteome Software Inc)
86
Proteome Software Inc scaffold dia v 2 0 0
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Scaffold Dia V 2 0 0, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/dia+scaffold/10__21203_slash_rs__3__rs___1318442_slash_v1-172-5-8
Average 86 stars, based on 1 article reviews
scaffold dia v 2 0 0 - by Bioz Stars, 2026-09
86/100 stars
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bionanosolve  (BioNano Genomics)
90
BioNano Genomics bionanosolve
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Bionanosolve, supplied by BioNano Genomics, 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/computer+program+scaffold+version+4%2E6/bionano+solve+v3+2+1/pmc08290290-324-6-8
Average 90 stars, based on 1 article reviews
bionanosolve - by Bioz Stars, 2026-09
90/100 stars
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proteomic software scaffold  (Proteome Software Inc)
86
Proteome Software Inc proteomic software scaffold
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Proteomic Software Scaffold, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/3+pipeline+proteomic+scaffold+tpp+trans/pmc12545556__mmc1-127-11-16
Average 86 stars, based on 1 article reviews
proteomic software scaffold - by Bioz Stars, 2026-09
86/100 stars
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scaffold dda v6 5  (Proteome Software Inc)
86
Proteome Software Inc scaffold dda v6 5
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Scaffold Dda V6 5, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/dda+scaffold+software/pmc12816245-143-5-8
Average 86 stars, based on 1 article reviews
scaffold dda v6 5 - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier
scaffold 4 software  (Proteome Software Inc)
86
Proteome Software Inc scaffold 4 software
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Scaffold 4 Software, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/scaffold+software/pm30134841-442-13-18
Average 86 stars, based on 1 article reviews
scaffold 4 software - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier
scaffold 4  (Proteome Software Inc)
86
Proteome Software Inc scaffold 4
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Scaffold 4, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/4+scaffold/10__51585_slash_gjvr__2025__2__0140-96-7-8
Average 86 stars, based on 1 article reviews
scaffold 4 - by Bioz Stars, 2026-09
86/100 stars
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dream kchip3 scaffold  (Proteome Software Inc)
86
Proteome Software Inc dream kchip3 scaffold
Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) <t>BioCAD</t> design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) <t>3D</t> printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.
Dream Kchip3 Scaffold, supplied by Proteome Software 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/computer+program+scaffold+version+4%2E6/dream+kchip3+scaffold/pm23019329-99-6-9
Average 86 stars, based on 1 article reviews
dream kchip3 scaffold - by Bioz Stars, 2026-09
86/100 stars
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Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) BioCAD design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) 3D printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.

Journal: International Journal of Bioprinting

Article Title: Bioprinting of Human Neural Tissues Using a Sustainable Marine Tunicate-Derived Bioink for Translational Medicine Applications

doi: 10.18063/ijb.v8i4.604

Figure Lengend Snippet: Standardization of bioink on rheology, printability, cross-linking, and bioprinting of neural tissue constructs. (A) 10% tunicate hydrogel in NSC media is extruded into PBS, and the filament is not dense enough to free flow into the solution, as shown by its upward push when it extrudes into the solution. The filaments broke and fell into the solution when extruded continuously. (B) 10% tunicate gel + 26% Matrigel in NSC media in PBS, the filament is smoothly flowing into the solution. The filaments broke and fell into the solution when extruded continuously for a longer time. (C) 10% tunicate gel in NSC media extruded into the crosslinking solution (250 mM CaCl 2 ) gets cross-linked but lack smooth flow. (D) 10% tunicate gel + 26% Matrigel in NSC media extruded into the cross-linking solution (250 mM CaCl 2 ) shows a seamless extrusion. (E) Filament formation of 10% tunicate hydrogel in NSC media without Matrigel. (F) Filament formation of 10% tunicate gel + 26% Matrigel in NSC media. (G) Droplet formation of 10% tunicate hydrogel in NSC media without Matrigel at the tip of the needle. (H) Droplet formation of 10% tunicate gel +26% Matrigel in NSC media at the tip of the needle. (I) BioCAD design of the tissue construct. (J) Tool path generated using the BioCAD software showing the direction of print head movement. The numbers represent the steps in print head movement. (K) The shear modulus of the hydrogel. (L) Lattice coordinate profile showing structural uniformity of the two layered structure. The upward wave shows the mean struct length and the downward wave shows the total strut thickness. (M) 3D printed lattices in layers ranging from 1 to 10, showing the printability of the hydrogel. (N) Bioprinted tissue constructs in a 24-well plate printed using the well editor software plugin. The dimensions of the bioprinted tissue constructs were 8 mm × 8 mm × 1 mm. Alcian blue dye was used to enhance the visibility of cell-free hydrogel filaments. Neural tissue constructs were printed without the dye.

Article Snippet: Scaffolds were designed and fabricated using RegenHU 3D Discovery printer BioCAD software (RegenHU, Switzerland).

Techniques: Construct, Generated, Software, Shear