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GenScript corporation cell-adhesive peptide gcgygrgdspg (molecular weight [mw]: 1025.1 da, referred to as rgd peptide from here on)
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A Norbornene groups were functionalized along the HA backbone in low, medium, or high frequency based on parameters during the synthesis process. B Lyophilized NorHA polymer was dissolved in complete cell media, along with Irgacure 2959, a <t>RGD</t> peptide (G <t>C</t> <t>GYGRGDSPG),</t> and an MMP-sensitive crosslinker (G C RDGPQG ↓ IWGQDR C G; down arrow indicates the site of proteolytic cleavage). The pre-polymer solution was then cast in a cylindrical mold and crosslinked with UV light to yield a hydrogel with human LECs encapsulated throughout. C Several days after encapsulation, LECs self-assembled into vessels to varying extents based on the hydrogel conditions. These engineered in vitro constructs, created with a fully defined matrix and growth factor components along with only human LECs and no feeder layers or support cells, can be used in mechanistic and growth factor screenings, for disease modeling, and as a therapeutic transplant. Schematic was created with BioRender.com.
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A Norbornene groups were functionalized along the HA backbone in low, medium, or high frequency based on parameters during the synthesis process. B Lyophilized NorHA polymer was dissolved in complete cell media, along with Irgacure 2959, a <t>RGD</t> peptide (G <t>C</t> <t>GYGRGDSPG),</t> and an MMP-sensitive crosslinker (G C RDGPQG ↓ IWGQDR C G; down arrow indicates the site of proteolytic cleavage). The pre-polymer solution was then cast in a cylindrical mold and crosslinked with UV light to yield a hydrogel with human LECs encapsulated throughout. C Several days after encapsulation, LECs self-assembled into vessels to varying extents based on the hydrogel conditions. These engineered in vitro constructs, created with a fully defined matrix and growth factor components along with only human LECs and no feeder layers or support cells, can be used in mechanistic and growth factor screenings, for disease modeling, and as a therapeutic transplant. Schematic was created with BioRender.com.
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A Norbornene groups were functionalized along the HA backbone in low, medium, or high frequency based on parameters during the synthesis process. B Lyophilized NorHA polymer was dissolved in complete cell media, along with Irgacure 2959, a <t>RGD</t> peptide (G <t>C</t> <t>GYGRGDSPG),</t> and an MMP-sensitive crosslinker (G C RDGPQG ↓ IWGQDR C G; down arrow indicates the site of proteolytic cleavage). The pre-polymer solution was then cast in a cylindrical mold and crosslinked with UV light to yield a hydrogel with human LECs encapsulated throughout. C Several days after encapsulation, LECs self-assembled into vessels to varying extents based on the hydrogel conditions. These engineered in vitro constructs, created with a fully defined matrix and growth factor components along with only human LECs and no feeder layers or support cells, can be used in mechanistic and growth factor screenings, for disease modeling, and as a therapeutic transplant. Schematic was created with BioRender.com.
High Molecular Weight Ha (Hmw Ha, 1500–1800 Kda, Reference 53,747, supplied by Millipore, 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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Bio-Rad reference molecular weight protein marker
A Norbornene groups were functionalized along the HA backbone in low, medium, or high frequency based on parameters during the synthesis process. B Lyophilized NorHA polymer was dissolved in complete cell media, along with Irgacure 2959, a <t>RGD</t> peptide (G <t>C</t> <t>GYGRGDSPG),</t> and an MMP-sensitive crosslinker (G C RDGPQG ↓ IWGQDR C G; down arrow indicates the site of proteolytic cleavage). The pre-polymer solution was then cast in a cylindrical mold and crosslinked with UV light to yield a hydrogel with human LECs encapsulated throughout. C Several days after encapsulation, LECs self-assembled into vessels to varying extents based on the hydrogel conditions. These engineered in vitro constructs, created with a fully defined matrix and growth factor components along with only human LECs and no feeder layers or support cells, can be used in mechanistic and growth factor screenings, for disease modeling, and as a therapeutic transplant. Schematic was created with BioRender.com.
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EuroClone reference sharpmasstm vi protein molecular weight marker
A Norbornene groups were functionalized along the HA backbone in low, medium, or high frequency based on parameters during the synthesis process. B Lyophilized NorHA polymer was dissolved in complete cell media, along with Irgacure 2959, a <t>RGD</t> peptide (G <t>C</t> <t>GYGRGDSPG),</t> and an MMP-sensitive crosslinker (G C RDGPQG ↓ IWGQDR C G; down arrow indicates the site of proteolytic cleavage). The pre-polymer solution was then cast in a cylindrical mold and crosslinked with UV light to yield a hydrogel with human LECs encapsulated throughout. C Several days after encapsulation, LECs self-assembled into vessels to varying extents based on the hydrogel conditions. These engineered in vitro constructs, created with a fully defined matrix and growth factor components along with only human LECs and no feeder layers or support cells, can be used in mechanistic and growth factor screenings, for disease modeling, and as a therapeutic transplant. Schematic was created with BioRender.com.
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Bio-Rad reference protein molecular weight ladder
A Norbornene groups were functionalized along the HA backbone in low, medium, or high frequency based on parameters during the synthesis process. B Lyophilized NorHA polymer was dissolved in complete cell media, along with Irgacure 2959, a <t>RGD</t> peptide (G <t>C</t> <t>GYGRGDSPG),</t> and an MMP-sensitive crosslinker (G C RDGPQG ↓ IWGQDR C G; down arrow indicates the site of proteolytic cleavage). The pre-polymer solution was then cast in a cylindrical mold and crosslinked with UV light to yield a hydrogel with human LECs encapsulated throughout. C Several days after encapsulation, LECs self-assembled into vessels to varying extents based on the hydrogel conditions. These engineered in vitro constructs, created with a fully defined matrix and growth factor components along with only human LECs and no feeder layers or support cells, can be used in mechanistic and growth factor screenings, for disease modeling, and as a therapeutic transplant. Schematic was created with BioRender.com.
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Image Search Results


A Norbornene groups were functionalized along the HA backbone in low, medium, or high frequency based on parameters during the synthesis process. B Lyophilized NorHA polymer was dissolved in complete cell media, along with Irgacure 2959, a RGD peptide (G C GYGRGDSPG), and an MMP-sensitive crosslinker (G C RDGPQG ↓ IWGQDR C G; down arrow indicates the site of proteolytic cleavage). The pre-polymer solution was then cast in a cylindrical mold and crosslinked with UV light to yield a hydrogel with human LECs encapsulated throughout. C Several days after encapsulation, LECs self-assembled into vessels to varying extents based on the hydrogel conditions. These engineered in vitro constructs, created with a fully defined matrix and growth factor components along with only human LECs and no feeder layers or support cells, can be used in mechanistic and growth factor screenings, for disease modeling, and as a therapeutic transplant. Schematic was created with BioRender.com.

Journal: Communications Biology

Article Title: Multi-parameter tunable synthetic matrix for engineering lymphatic vessels

doi: 10.1038/s42003-024-06935-7

Figure Lengend Snippet: A Norbornene groups were functionalized along the HA backbone in low, medium, or high frequency based on parameters during the synthesis process. B Lyophilized NorHA polymer was dissolved in complete cell media, along with Irgacure 2959, a RGD peptide (G C GYGRGDSPG), and an MMP-sensitive crosslinker (G C RDGPQG ↓ IWGQDR C G; down arrow indicates the site of proteolytic cleavage). The pre-polymer solution was then cast in a cylindrical mold and crosslinked with UV light to yield a hydrogel with human LECs encapsulated throughout. C Several days after encapsulation, LECs self-assembled into vessels to varying extents based on the hydrogel conditions. These engineered in vitro constructs, created with a fully defined matrix and growth factor components along with only human LECs and no feeder layers or support cells, can be used in mechanistic and growth factor screenings, for disease modeling, and as a therapeutic transplant. Schematic was created with BioRender.com.

Article Snippet: We obtained the cell-adhesive peptide G C GYGRGDSPG (molecular weight [MW]: 1025.1 Da, referred to as RGD peptide from here on), cell-nonadhesive peptide GCGYGRDGSPG (MW: 1025.1 Da, referred to as RDG peptide from here on), and MMP-sensitive peptide crosslinker G C RDGPQG ↓ IWGQDR C G (MW: 1754.0 Da; down arrow indicates the site of proteolytic cleavage) from GenScript Corporation.

Techniques: Polymer, Encapsulation, In Vitro, Construct