primovert light microscopy Search Results


transmitted light microscope primo vert  (Carl Zeiss)
96
Carl Zeiss transmitted light microscope primo vert
Transmitted Light Microscope Primo Vert, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primovert+light+microscopy/Microscope+Primovert/pm33126019-338-12-17
Average 96 stars, based on 1 article reviews
transmitted light microscope primo vert - by Bioz Stars, 2026-11
96/100 stars
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primovert phase contrast light microscope  (Carl Zeiss)
99
Carl Zeiss primovert phase contrast light microscope
Primovert Phase Contrast Light Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primovert+light+microscopy/Primovert+Compact+Inverted+Microscope/10__24075_slash_brsmu__2024__007-67-37-42
Average 99 stars, based on 1 article reviews
primovert phase contrast light microscope - by Bioz Stars, 2026-11
99/100 stars
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zeiss primovert hdcam  (Carl Zeiss)
94
Carl Zeiss zeiss primovert hdcam
Figure 4. Human lens epithelial (HLE-B3) cells grown on uncoated and Ti3C2Tx-coated tissue grade 12-well plates. Wound closure rate was quantified using light microscope images taken at the selected time points (figure (A)). Light microscope images of HLE-B3 cells grown on uncoated (figures (B) and (D)) and Ti3C2Tx-coated (figures (C) and (E)) stained with crystal violet at t = 0 h (top) and t = 120 h (bottom). x50 magnification by light microscope (Zeiss <t>Primovert</t> <t>HDcam,</t> Germany). Scale bar: 25 µM. Measurements were calculated using Fiji Image J. Wound closure was calculated as the width difference in the scratch across the cell monolayer at t = 0 h relative to the other time points. A two-way ANOVA was completed using GraphPad Prism 5. ∗∗p < 0.01; ∗∗∗p < 0.001. (Uncoated: cells grown on tissue culture well; Ti3C2Tx-coated: cells grown on Ti3C2Tx-coated wells) (Mean ± SEM; n = 6).
Zeiss Primovert Hdcam, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primovert+light+microscopy/Microscope+Primovert+HDcam/10__1088_slash_2053___1583_slash_ac95a7-107-13-16
Average 94 stars, based on 1 article reviews
zeiss primovert hdcam - by Bioz Stars, 2026-11
94/100 stars
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primovert iled gttingen  (Carl Zeiss)
93
Carl Zeiss primovert iled gttingen
Figure 4. Human lens epithelial (HLE-B3) cells grown on uncoated and Ti3C2Tx-coated tissue grade 12-well plates. Wound closure rate was quantified using light microscope images taken at the selected time points (figure (A)). Light microscope images of HLE-B3 cells grown on uncoated (figures (B) and (D)) and Ti3C2Tx-coated (figures (C) and (E)) stained with crystal violet at t = 0 h (top) and t = 120 h (bottom). x50 magnification by light microscope (Zeiss <t>Primovert</t> <t>HDcam,</t> Germany). Scale bar: 25 µM. Measurements were calculated using Fiji Image J. Wound closure was calculated as the width difference in the scratch across the cell monolayer at t = 0 h relative to the other time points. A two-way ANOVA was completed using GraphPad Prism 5. ∗∗p < 0.01; ∗∗∗p < 0.001. (Uncoated: cells grown on tissue culture well; Ti3C2Tx-coated: cells grown on Ti3C2Tx-coated wells) (Mean ± SEM; n = 6).
Primovert Iled Gttingen, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primovert+light+microscopy/Microscope+Primovert+iLED/pmc09990328-36-19-18
Average 93 stars, based on 1 article reviews
primovert iled gttingen - by Bioz Stars, 2026-11
93/100 stars
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light microscope  (Carl Zeiss)
94
Carl Zeiss light microscope
Figure 4. Human lens epithelial (HLE-B3) cells grown on uncoated and Ti3C2Tx-coated tissue grade 12-well plates. Wound closure rate was quantified using light microscope images taken at the selected time points (figure (A)). Light microscope images of HLE-B3 cells grown on uncoated (figures (B) and (D)) and Ti3C2Tx-coated (figures (C) and (E)) stained with crystal violet at t = 0 h (top) and t = 120 h (bottom). x50 magnification by light microscope (Zeiss <t>Primovert</t> <t>HDcam,</t> Germany). Scale bar: 25 µM. Measurements were calculated using Fiji Image J. Wound closure was calculated as the width difference in the scratch across the cell monolayer at t = 0 h relative to the other time points. A two-way ANOVA was completed using GraphPad Prism 5. ∗∗p < 0.01; ∗∗∗p < 0.001. (Uncoated: cells grown on tissue culture well; Ti3C2Tx-coated: cells grown on Ti3C2Tx-coated wells) (Mean ± SEM; n = 6).
Light Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primovert+light+microscopy/Primovert+microscope+stand+with+binocular+phototube/pm35609749-69-8-13
Average 94 stars, based on 1 article reviews
light microscope - by Bioz Stars, 2026-11
94/100 stars
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light microscopes  (Nikon)
99
Nikon light microscopes
Figure 4. Human lens epithelial (HLE-B3) cells grown on uncoated and Ti3C2Tx-coated tissue grade 12-well plates. Wound closure rate was quantified using light microscope images taken at the selected time points (figure (A)). Light microscope images of HLE-B3 cells grown on uncoated (figures (B) and (D)) and Ti3C2Tx-coated (figures (C) and (E)) stained with crystal violet at t = 0 h (top) and t = 120 h (bottom). x50 magnification by light microscope (Zeiss <t>Primovert</t> <t>HDcam,</t> Germany). Scale bar: 25 µM. Measurements were calculated using Fiji Image J. Wound closure was calculated as the width difference in the scratch across the cell monolayer at t = 0 h relative to the other time points. A two-way ANOVA was completed using GraphPad Prism 5. ∗∗p < 0.01; ∗∗∗p < 0.001. (Uncoated: cells grown on tissue culture well; Ti3C2Tx-coated: cells grown on Ti3C2Tx-coated wells) (Mean ± SEM; n = 6).
Light Microscopes, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primovert+light+microscopy/Inverted+Microscopes/pm32404074-97-5-10
Average 99 stars, based on 1 article reviews
light microscopes - by Bioz Stars, 2026-11
99/100 stars
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upright light microscope  (Carl Zeiss)
96
Carl Zeiss upright light microscope
Figure 4. Human lens epithelial (HLE-B3) cells grown on uncoated and Ti3C2Tx-coated tissue grade 12-well plates. Wound closure rate was quantified using light microscope images taken at the selected time points (figure (A)). Light microscope images of HLE-B3 cells grown on uncoated (figures (B) and (D)) and Ti3C2Tx-coated (figures (C) and (E)) stained with crystal violet at t = 0 h (top) and t = 120 h (bottom). x50 magnification by light microscope (Zeiss <t>Primovert</t> <t>HDcam,</t> Germany). Scale bar: 25 µM. Measurements were calculated using Fiji Image J. Wound closure was calculated as the width difference in the scratch across the cell monolayer at t = 0 h relative to the other time points. A two-way ANOVA was completed using GraphPad Prism 5. ∗∗p < 0.01; ∗∗∗p < 0.001. (Uncoated: cells grown on tissue culture well; Ti3C2Tx-coated: cells grown on Ti3C2Tx-coated wells) (Mean ± SEM; n = 6).
Upright Light Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primovert+light+microscopy/Primovert+microscope+stand+with+binocular+tube/10__1016_slash_j__chempr__2024__07__012-107-18-21
Average 96 stars, based on 1 article reviews
upright light microscope - by Bioz Stars, 2026-11
96/100 stars
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primovert compact inverted microscope  (Darwin Microfluidics)
99
Darwin Microfluidics primovert compact inverted microscope
Figure 4. Human lens epithelial (HLE-B3) cells grown on uncoated and Ti3C2Tx-coated tissue grade 12-well plates. Wound closure rate was quantified using light microscope images taken at the selected time points (figure (A)). Light microscope images of HLE-B3 cells grown on uncoated (figures (B) and (D)) and Ti3C2Tx-coated (figures (C) and (E)) stained with crystal violet at t = 0 h (top) and t = 120 h (bottom). x50 magnification by light microscope (Zeiss <t>Primovert</t> <t>HDcam,</t> Germany). Scale bar: 25 µM. Measurements were calculated using Fiji Image J. Wound closure was calculated as the width difference in the scratch across the cell monolayer at t = 0 h relative to the other time points. A two-way ANOVA was completed using GraphPad Prism 5. ∗∗p < 0.01; ∗∗∗p < 0.001. (Uncoated: cells grown on tissue culture well; Ti3C2Tx-coated: cells grown on Ti3C2Tx-coated wells) (Mean ± SEM; n = 6).
Primovert Compact Inverted Microscope, supplied by Darwin Microfluidics, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primovert+light+microscopy/Primovert+Compact+Inverted+Microscope/custom%40ps-200002174%4031035014
Average 99 stars, based on 1 article reviews
primovert compact inverted microscope - by Bioz Stars, 2026-11
99/100 stars
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Image Search Results


Figure 4. Human lens epithelial (HLE-B3) cells grown on uncoated and Ti3C2Tx-coated tissue grade 12-well plates. Wound closure rate was quantified using light microscope images taken at the selected time points (figure (A)). Light microscope images of HLE-B3 cells grown on uncoated (figures (B) and (D)) and Ti3C2Tx-coated (figures (C) and (E)) stained with crystal violet at t = 0 h (top) and t = 120 h (bottom). x50 magnification by light microscope (Zeiss Primovert HDcam, Germany). Scale bar: 25 µM. Measurements were calculated using Fiji Image J. Wound closure was calculated as the width difference in the scratch across the cell monolayer at t = 0 h relative to the other time points. A two-way ANOVA was completed using GraphPad Prism 5. ∗∗p < 0.01; ∗∗∗p < 0.001. (Uncoated: cells grown on tissue culture well; Ti3C2Tx-coated: cells grown on Ti3C2Tx-coated wells) (Mean ± SEM; n = 6).

Journal: 2D Materials

Article Title: Positive resolution of the wound-healing response in lens epithelial cells by Ti3C2T x MXene coatings for use in accommodative intraocular lens devices

doi: 10.1088/2053-1583/ac95a7

Figure Lengend Snippet: Figure 4. Human lens epithelial (HLE-B3) cells grown on uncoated and Ti3C2Tx-coated tissue grade 12-well plates. Wound closure rate was quantified using light microscope images taken at the selected time points (figure (A)). Light microscope images of HLE-B3 cells grown on uncoated (figures (B) and (D)) and Ti3C2Tx-coated (figures (C) and (E)) stained with crystal violet at t = 0 h (top) and t = 120 h (bottom). x50 magnification by light microscope (Zeiss Primovert HDcam, Germany). Scale bar: 25 µM. Measurements were calculated using Fiji Image J. Wound closure was calculated as the width difference in the scratch across the cell monolayer at t = 0 h relative to the other time points. A two-way ANOVA was completed using GraphPad Prism 5. ∗∗p < 0.01; ∗∗∗p < 0.001. (Uncoated: cells grown on tissue culture well; Ti3C2Tx-coated: cells grown on Ti3C2Tx-coated wells) (Mean ± SEM; n = 6).

Article Snippet: Images were captured at 0, 24, 48, 72 and 120 h using a Zeiss Primovert HDcam (Carl Zeiss Microscopy GmbH, Germany).

Techniques: Light Microscopy, Staining