imaging analysis software definiens tissue studio (version 3.60) Search Results


97
Danaher Inc leica mica
Leica Mica, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/pmc11339336__41467_2024_51402_MOESM1_ESM-62-20-20?v=Danaher+Inc
Average 97 stars, based on 1 article reviews
leica mica - by Bioz Stars, 2026-07
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Bio-Rad gs 363 molecular imager system
Gs 363 Molecular Imager System, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
gs 363 molecular imager system - by Bioz Stars, 2026-07
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Carl Zeiss supra 55 feg-vp
Supra 55 Feg Vp, supplied by Carl Zeiss, 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/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/10__21577_slash_0103___5053__20180181-37-18-17?v=Carl+Zeiss
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Neurolucida 360 Software, supplied by MBF Bioscience, 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/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/pmc06849109__mmc1-234-6-9?v=MBF+Bioscience
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Average 86 stars, based on 1 article reviews
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Automated Metaphase Finder Program Duet Scanning Imaging Workstation, supplied by BioView Inc, 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/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/pmc10831274-254-11-15?v=BioView+Inc
Average 90 stars, based on 1 article reviews
automated metaphase finder program duet scanning imaging workstation - by Bioz Stars, 2026-07
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Nikon ez c1 3 60 software
Ez C1 3 60 Software, 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/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/pmc05786178-646-5-8?v=Nikon
Average 99 stars, based on 1 article reviews
ez c1 3 60 software - by Bioz Stars, 2026-07
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Carl Zeiss gemini 360 fesem
Genetic design of E. coli to produce the functional curli nanofibers to covalently crosslink ( a ) CL1: SpyTag and SpyCatcher (SpyCat) domains fused to CsgA, ( b ) CL2: SpyTag and SpyCat domains fused to CsgA via the Spacer. c Representative stress-strain curves of MECHS films consisting of CsgA, CL1, and CL2 with 3% plasticizer. d Young’s modulus, and ( e ) Elongation at the break for CsgA, CL1, and CL2 with 3% plasticizer. Biological replicates n = 10 for CsgA, n = 15 for CL1, and n = 20 for CL2. Data represented as mean ± standard deviation. d * p = 0.01, * p = 0.0295. e **** p < 0.0001. One-way ANOVA followed by Tukey’s multiple comparisons test. f Representative photographs showing a tensile test of CL1 film with the lateral dimension of 0.5 cm by 4 cm. Left image: initial. Right image: before the break. g Plot of normalized Congo Red absorbance and the weights of wet cell pellets. For Congo Red absorbance, biological replicates n = 3 for Sham and n = 6 for CsgA, CL1 and CL2. For weights of wet cell pellets, biological replicates n = 3 for Sham and n = 10 for CsgA, CL1 and CL2. h Plot of the estimated wet weight of curli nanofibers and the wet weight percentage of estimated curli nanofibers to the cell pellet. Biological replicates n = 6 for the wet weight of curli nanofibers and n = 3 for the percentage weight. Data represented as mean ± standard deviation. i Field Emission Scanning Electron Microscopy <t>(FESEM)</t> images of CsgA, CL1 and CL2. Top row: cell cultures. Scale bar 1 μm. Middle row: Top view of MECHS. Scale bar 10 μm. Bottom row: Side view of MECHS. Scale bar 10 μm.
Gemini 360 Fesem, supplied by Carl Zeiss, 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/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/pmc11557937-222-5-5?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
gemini 360 fesem - by Bioz Stars, 2026-07
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90
Nidek CO gonioscope gs-1
Genetic design of E. coli to produce the functional curli nanofibers to covalently crosslink ( a ) CL1: SpyTag and SpyCatcher (SpyCat) domains fused to CsgA, ( b ) CL2: SpyTag and SpyCat domains fused to CsgA via the Spacer. c Representative stress-strain curves of MECHS films consisting of CsgA, CL1, and CL2 with 3% plasticizer. d Young’s modulus, and ( e ) Elongation at the break for CsgA, CL1, and CL2 with 3% plasticizer. Biological replicates n = 10 for CsgA, n = 15 for CL1, and n = 20 for CL2. Data represented as mean ± standard deviation. d * p = 0.01, * p = 0.0295. e **** p < 0.0001. One-way ANOVA followed by Tukey’s multiple comparisons test. f Representative photographs showing a tensile test of CL1 film with the lateral dimension of 0.5 cm by 4 cm. Left image: initial. Right image: before the break. g Plot of normalized Congo Red absorbance and the weights of wet cell pellets. For Congo Red absorbance, biological replicates n = 3 for Sham and n = 6 for CsgA, CL1 and CL2. For weights of wet cell pellets, biological replicates n = 3 for Sham and n = 10 for CsgA, CL1 and CL2. h Plot of the estimated wet weight of curli nanofibers and the wet weight percentage of estimated curli nanofibers to the cell pellet. Biological replicates n = 6 for the wet weight of curli nanofibers and n = 3 for the percentage weight. Data represented as mean ± standard deviation. i Field Emission Scanning Electron Microscopy <t>(FESEM)</t> images of CsgA, CL1 and CL2. Top row: cell cultures. Scale bar 1 μm. Middle row: Top view of MECHS. Scale bar 10 μm. Bottom row: Side view of MECHS. Scale bar 10 μm.
Gonioscope Gs 1, supplied by Nidek CO, 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/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/med_rxiv__2022__06__22__22276741-98-11-10?v=Nidek+CO
Average 90 stars, based on 1 article reviews
gonioscope gs-1 - by Bioz Stars, 2026-07
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98
Coherent Corp tirf mode
Genetic design of E. coli to produce the functional curli nanofibers to covalently crosslink ( a ) CL1: SpyTag and SpyCatcher (SpyCat) domains fused to CsgA, ( b ) CL2: SpyTag and SpyCat domains fused to CsgA via the Spacer. c Representative stress-strain curves of MECHS films consisting of CsgA, CL1, and CL2 with 3% plasticizer. d Young’s modulus, and ( e ) Elongation at the break for CsgA, CL1, and CL2 with 3% plasticizer. Biological replicates n = 10 for CsgA, n = 15 for CL1, and n = 20 for CL2. Data represented as mean ± standard deviation. d * p = 0.01, * p = 0.0295. e **** p < 0.0001. One-way ANOVA followed by Tukey’s multiple comparisons test. f Representative photographs showing a tensile test of CL1 film with the lateral dimension of 0.5 cm by 4 cm. Left image: initial. Right image: before the break. g Plot of normalized Congo Red absorbance and the weights of wet cell pellets. For Congo Red absorbance, biological replicates n = 3 for Sham and n = 6 for CsgA, CL1 and CL2. For weights of wet cell pellets, biological replicates n = 3 for Sham and n = 10 for CsgA, CL1 and CL2. h Plot of the estimated wet weight of curli nanofibers and the wet weight percentage of estimated curli nanofibers to the cell pellet. Biological replicates n = 6 for the wet weight of curli nanofibers and n = 3 for the percentage weight. Data represented as mean ± standard deviation. i Field Emission Scanning Electron Microscopy <t>(FESEM)</t> images of CsgA, CL1 and CL2. Top row: cell cultures. Scale bar 1 μm. Middle row: Top view of MECHS. Scale bar 10 μm. Bottom row: Side view of MECHS. Scale bar 10 μm.
Tirf Mode, supplied by Coherent Corp, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/bio_rxiv__2024__01__20__576357-369-4-15?v=Coherent+Corp
Average 98 stars, based on 1 article reviews
tirf mode - by Bioz Stars, 2026-07
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99
Danaher Inc application suite las x software version number 3 6 0 20104
Genetic design of E. coli to produce the functional curli nanofibers to covalently crosslink ( a ) CL1: SpyTag and SpyCatcher (SpyCat) domains fused to CsgA, ( b ) CL2: SpyTag and SpyCat domains fused to CsgA via the Spacer. c Representative stress-strain curves of MECHS films consisting of CsgA, CL1, and CL2 with 3% plasticizer. d Young’s modulus, and ( e ) Elongation at the break for CsgA, CL1, and CL2 with 3% plasticizer. Biological replicates n = 10 for CsgA, n = 15 for CL1, and n = 20 for CL2. Data represented as mean ± standard deviation. d * p = 0.01, * p = 0.0295. e **** p < 0.0001. One-way ANOVA followed by Tukey’s multiple comparisons test. f Representative photographs showing a tensile test of CL1 film with the lateral dimension of 0.5 cm by 4 cm. Left image: initial. Right image: before the break. g Plot of normalized Congo Red absorbance and the weights of wet cell pellets. For Congo Red absorbance, biological replicates n = 3 for Sham and n = 6 for CsgA, CL1 and CL2. For weights of wet cell pellets, biological replicates n = 3 for Sham and n = 10 for CsgA, CL1 and CL2. h Plot of the estimated wet weight of curli nanofibers and the wet weight percentage of estimated curli nanofibers to the cell pellet. Biological replicates n = 6 for the wet weight of curli nanofibers and n = 3 for the percentage weight. Data represented as mean ± standard deviation. i Field Emission Scanning Electron Microscopy <t>(FESEM)</t> images of CsgA, CL1 and CL2. Top row: cell cultures. Scale bar 1 μm. Middle row: Top view of MECHS. Scale bar 10 μm. Bottom row: Side view of MECHS. Scale bar 10 μm.
Application Suite Las X Software Version Number 3 6 0 20104, supplied by Danaher Inc, 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/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/pm40508225-150-14-22?v=Danaher+Inc
Average 99 stars, based on 1 article reviews
application suite las x software version number 3 6 0 20104 - by Bioz Stars, 2026-07
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90
LEO Electron Microscopy Inc leo stereoscan 360 sem
Genetic design of E. coli to produce the functional curli nanofibers to covalently crosslink ( a ) CL1: SpyTag and SpyCatcher (SpyCat) domains fused to CsgA, ( b ) CL2: SpyTag and SpyCat domains fused to CsgA via the Spacer. c Representative stress-strain curves of MECHS films consisting of CsgA, CL1, and CL2 with 3% plasticizer. d Young’s modulus, and ( e ) Elongation at the break for CsgA, CL1, and CL2 with 3% plasticizer. Biological replicates n = 10 for CsgA, n = 15 for CL1, and n = 20 for CL2. Data represented as mean ± standard deviation. d * p = 0.01, * p = 0.0295. e **** p < 0.0001. One-way ANOVA followed by Tukey’s multiple comparisons test. f Representative photographs showing a tensile test of CL1 film with the lateral dimension of 0.5 cm by 4 cm. Left image: initial. Right image: before the break. g Plot of normalized Congo Red absorbance and the weights of wet cell pellets. For Congo Red absorbance, biological replicates n = 3 for Sham and n = 6 for CsgA, CL1 and CL2. For weights of wet cell pellets, biological replicates n = 3 for Sham and n = 10 for CsgA, CL1 and CL2. h Plot of the estimated wet weight of curli nanofibers and the wet weight percentage of estimated curli nanofibers to the cell pellet. Biological replicates n = 6 for the wet weight of curli nanofibers and n = 3 for the percentage weight. Data represented as mean ± standard deviation. i Field Emission Scanning Electron Microscopy <t>(FESEM)</t> images of CsgA, CL1 and CL2. Top row: cell cultures. Scale bar 1 μm. Middle row: Top view of MECHS. Scale bar 10 μm. Bottom row: Side view of MECHS. Scale bar 10 μm.
Leo Stereoscan 360 Sem, supplied by LEO Electron Microscopy Inc, 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/imaging+analysis+software+definiens+tissue+studio+%28version+3%2E60%29/pmc04242390-174-33-37?v=LEO+Electron+Microscopy+Inc
Average 90 stars, based on 1 article reviews
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Image Search Results


Genetic design of E. coli to produce the functional curli nanofibers to covalently crosslink ( a ) CL1: SpyTag and SpyCatcher (SpyCat) domains fused to CsgA, ( b ) CL2: SpyTag and SpyCat domains fused to CsgA via the Spacer. c Representative stress-strain curves of MECHS films consisting of CsgA, CL1, and CL2 with 3% plasticizer. d Young’s modulus, and ( e ) Elongation at the break for CsgA, CL1, and CL2 with 3% plasticizer. Biological replicates n = 10 for CsgA, n = 15 for CL1, and n = 20 for CL2. Data represented as mean ± standard deviation. d * p = 0.01, * p = 0.0295. e **** p < 0.0001. One-way ANOVA followed by Tukey’s multiple comparisons test. f Representative photographs showing a tensile test of CL1 film with the lateral dimension of 0.5 cm by 4 cm. Left image: initial. Right image: before the break. g Plot of normalized Congo Red absorbance and the weights of wet cell pellets. For Congo Red absorbance, biological replicates n = 3 for Sham and n = 6 for CsgA, CL1 and CL2. For weights of wet cell pellets, biological replicates n = 3 for Sham and n = 10 for CsgA, CL1 and CL2. h Plot of the estimated wet weight of curli nanofibers and the wet weight percentage of estimated curli nanofibers to the cell pellet. Biological replicates n = 6 for the wet weight of curli nanofibers and n = 3 for the percentage weight. Data represented as mean ± standard deviation. i Field Emission Scanning Electron Microscopy (FESEM) images of CsgA, CL1 and CL2. Top row: cell cultures. Scale bar 1 μm. Middle row: Top view of MECHS. Scale bar 10 μm. Bottom row: Side view of MECHS. Scale bar 10 μm.

Journal: Nature Communications

Article Title: Mechanically Tunable, Compostable, Healable and Scalable Engineered Living Materials

doi: 10.1038/s41467-024-53052-4

Figure Lengend Snippet: Genetic design of E. coli to produce the functional curli nanofibers to covalently crosslink ( a ) CL1: SpyTag and SpyCatcher (SpyCat) domains fused to CsgA, ( b ) CL2: SpyTag and SpyCat domains fused to CsgA via the Spacer. c Representative stress-strain curves of MECHS films consisting of CsgA, CL1, and CL2 with 3% plasticizer. d Young’s modulus, and ( e ) Elongation at the break for CsgA, CL1, and CL2 with 3% plasticizer. Biological replicates n = 10 for CsgA, n = 15 for CL1, and n = 20 for CL2. Data represented as mean ± standard deviation. d * p = 0.01, * p = 0.0295. e **** p < 0.0001. One-way ANOVA followed by Tukey’s multiple comparisons test. f Representative photographs showing a tensile test of CL1 film with the lateral dimension of 0.5 cm by 4 cm. Left image: initial. Right image: before the break. g Plot of normalized Congo Red absorbance and the weights of wet cell pellets. For Congo Red absorbance, biological replicates n = 3 for Sham and n = 6 for CsgA, CL1 and CL2. For weights of wet cell pellets, biological replicates n = 3 for Sham and n = 10 for CsgA, CL1 and CL2. h Plot of the estimated wet weight of curli nanofibers and the wet weight percentage of estimated curli nanofibers to the cell pellet. Biological replicates n = 6 for the wet weight of curli nanofibers and n = 3 for the percentage weight. Data represented as mean ± standard deviation. i Field Emission Scanning Electron Microscopy (FESEM) images of CsgA, CL1 and CL2. Top row: cell cultures. Scale bar 1 μm. Middle row: Top view of MECHS. Scale bar 10 μm. Bottom row: Side view of MECHS. Scale bar 10 μm.

Article Snippet: Images were acquired using a Zeiss Gemini 360 FESEM equipped with a field emission gun operating at 5–10 kV.

Techniques: Functional Assay, Standard Deviation, Electron Microscopy

Representative photographs showing the biodegradation of MECHS and toilet paper in ( a ) a fresh fishnure ( b ) a dry fishnure. The lateral dimensions of the MECHS film and the toilet paper were 5 cm by 5 cm. c Plot shows the normalized biodegradation weight loss of MECHS (CsgA, CL1, and CL2), toilet paper, kimwipe (KW), polyvinyl alcohol - Mckesson (PVA-Mc), cellulose acetate (CA), poly-L-lactic acid (PLLA), polyethylene terephthalate (PET) and low-density polyethylene (LDPE). Biological replicates n = 3 for CsgA, CL1 and CL2. Technical replicates n = 3 for paper, KW, PVA-Mc, CA, PLLA, PET, and LDPE. Data represented as mean ± standard deviation. Photographs show the dissolution of d MECHS e toilet paper, f PVA-Mc, and g polyvinyl alcohol - Superpunch (PVA-Sp). d – g Lateral dimension of the films was 1 cm by 5 cm. h Photograph of a black bean seedling grown in the soil mixed with fishnure (comprising biodegraded MECHS) in a 9:1 ratio. i FESEM image of MECHS film healed by placing microliters of water at the site of abrasion (black arrows). Scale bar 200 μm. j Photograph shows the MECHS films welded (black arrows) by using water. Scale bar 0.5 cm.

Journal: Nature Communications

Article Title: Mechanically Tunable, Compostable, Healable and Scalable Engineered Living Materials

doi: 10.1038/s41467-024-53052-4

Figure Lengend Snippet: Representative photographs showing the biodegradation of MECHS and toilet paper in ( a ) a fresh fishnure ( b ) a dry fishnure. The lateral dimensions of the MECHS film and the toilet paper were 5 cm by 5 cm. c Plot shows the normalized biodegradation weight loss of MECHS (CsgA, CL1, and CL2), toilet paper, kimwipe (KW), polyvinyl alcohol - Mckesson (PVA-Mc), cellulose acetate (CA), poly-L-lactic acid (PLLA), polyethylene terephthalate (PET) and low-density polyethylene (LDPE). Biological replicates n = 3 for CsgA, CL1 and CL2. Technical replicates n = 3 for paper, KW, PVA-Mc, CA, PLLA, PET, and LDPE. Data represented as mean ± standard deviation. Photographs show the dissolution of d MECHS e toilet paper, f PVA-Mc, and g polyvinyl alcohol - Superpunch (PVA-Sp). d – g Lateral dimension of the films was 1 cm by 5 cm. h Photograph of a black bean seedling grown in the soil mixed with fishnure (comprising biodegraded MECHS) in a 9:1 ratio. i FESEM image of MECHS film healed by placing microliters of water at the site of abrasion (black arrows). Scale bar 200 μm. j Photograph shows the MECHS films welded (black arrows) by using water. Scale bar 0.5 cm.

Article Snippet: Images were acquired using a Zeiss Gemini 360 FESEM equipped with a field emission gun operating at 5–10 kV.

Techniques: Standard Deviation, Dissolution