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(a) Fluorescent images of CSP cells on GelMA microgels (left) and GelMA microgels coated with silica hydrogel (right), subjected to oxidative stress. The cells were stained with calcein-AM (green) and ethidium homodimer-1 (red) to visualize <t>live</t> and <t>dead</t> cells, respectively (scale bar: 50 μm). (b) Viability of the CSP cells was quantified as the percentage of the live cells (* p < 0.05).
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(a) Fluorescent images of CSP cells on GelMA microgels (left) and GelMA microgels coated with silica hydrogel (right), subjected to oxidative stress. The cells were stained with calcein-AM (green) and ethidium homodimer-1 (red) to visualize <t>live</t> and <t>dead</t> cells, respectively (scale bar: 50 μm). (b) Viability of the CSP cells was quantified as the percentage of the live cells (* p < 0.05).
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(a) Fluorescent images of CSP cells on GelMA microgels (left) and GelMA microgels coated with silica hydrogel (right), subjected to oxidative stress. The cells were stained with calcein-AM (green) and ethidium homodimer-1 (red) to visualize <t>live</t> and <t>dead</t> cells, respectively (scale bar: 50 μm). (b) Viability of the CSP cells was quantified as the percentage of the live cells (* p < 0.05).
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(a) Fluorescent images of CSP cells on GelMA microgels (left) and GelMA microgels coated with silica hydrogel (right), subjected to oxidative stress. The cells were stained with calcein-AM (green) and ethidium homodimer-1 (red) to visualize <t>live</t> and <t>dead</t> cells, respectively (scale bar: 50 μm). (b) Viability of the CSP cells was quantified as the percentage of the live cells (* p < 0.05).
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Image Search Results


(a) Fluorescent images of CSP cells on GelMA microgels (left) and GelMA microgels coated with silica hydrogel (right), subjected to oxidative stress. The cells were stained with calcein-AM (green) and ethidium homodimer-1 (red) to visualize live and dead cells, respectively (scale bar: 50 μm). (b) Viability of the CSP cells was quantified as the percentage of the live cells (* p < 0.05).

Journal: Biomacromolecules

Article Title: Microfluidics-Assisted Fabrication of Gelatin-Silica Core–Shell Microgels for Injectable Tissue Constructs

doi: 10.1021/bm401533y

Figure Lengend Snippet: (a) Fluorescent images of CSP cells on GelMA microgels (left) and GelMA microgels coated with silica hydrogel (right), subjected to oxidative stress. The cells were stained with calcein-AM (green) and ethidium homodimer-1 (red) to visualize live and dead cells, respectively (scale bar: 50 μm). (b) Viability of the CSP cells was quantified as the percentage of the live cells (* p < 0.05).

Article Snippet: After 1 h of incubation, the viability of cells on the microgels was evaluated using LIVE/DEAD Viability Kit (Invitrogen).

Techniques: Staining