confocal imaging Search Results


96
Danaher Inc image xpress micro confocal high content imaging system
Image Xpress Micro Confocal High Content Imaging System, supplied by Danaher Inc, 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/confocal+imaging/pm38249466-86-20-27?v=Danaher+Inc
Average 96 stars, based on 1 article reviews
image xpress micro confocal high content imaging system - by Bioz Stars, 2026-08
96/100 stars
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96
Danaher Inc imagexpress micro system
Imagexpress Micro System, supplied by Danaher Inc, 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/confocal+imaging/pmc04729552-150-6-9?v=Danaher+Inc
Average 96 stars, based on 1 article reviews
imagexpress micro system - by Bioz Stars, 2026-08
96/100 stars
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96
Olympus ixplore spin confocal imaging microscope
Ixplore Spin Confocal Imaging Microscope, supplied by Olympus, 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/confocal+imaging/pm41688788-189-5-10?v=Olympus
Average 96 stars, based on 1 article reviews
ixplore spin confocal imaging microscope - by Bioz Stars, 2026-08
96/100 stars
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91
Revvity operettar high content imaging system
Operettar High Content Imaging System, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/confocal+imaging/pm30101858-40-12-17?v=Revvity
Average 91 stars, based on 1 article reviews
operettar high content imaging system - by Bioz Stars, 2026-08
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99
Nikon laser confocal microscopy imaging system nikon ti2 e
Laser Confocal Microscopy Imaging System Nikon Ti2 E, 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/confocal+imaging/ppr0448535-77-5-10?v=Nikon
Average 99 stars, based on 1 article reviews
laser confocal microscopy imaging system nikon ti2 e - by Bioz Stars, 2026-08
99/100 stars
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90
heidelberg engineering corneal confocal images
Corneal Confocal Images, supplied by heidelberg engineering, 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/confocal+imaging/pmc03066470-164-7-1?v=heidelberg+engineering
Average 90 stars, based on 1 article reviews
corneal confocal images - by Bioz Stars, 2026-08
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90
Curiochips inc confocal fluorescence imaging of hlos differentiated directly on
Twenty-eight-day Curiochip HLO viability. (A) <t>HLOs</t> were plated <t>on</t> <t>Curiochips,</t> and output media was periodically assessed for albumin secretion (n = 16). (B) CYP450 gene expression was quantified from parallel time points after cell lysis (n = 3). Data were compared to day 14 Curiochips. (C) Day 7 Curiochip cultures were assessed for metabolic function by quantifying molecular turnover of acetaminophen (APAP) and darunavir (DRV) exclusively metabolized by CYP450s using LC/MS/MS; n = 3 and 16 for HLO and Curiochips, respectively. Data are expressed as mean ± standard error of the mean. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.
Confocal Fluorescence Imaging Of Hlos Differentiated Directly On, supplied by Curiochips 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/confocal+imaging/pmc11550169-135-12-16?v=Curiochips+inc
Average 90 stars, based on 1 article reviews
confocal fluorescence imaging of hlos differentiated directly on - by Bioz Stars, 2026-08
90/100 stars
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90
Nanonics Imaging Ltd cryogenic nsom/afm/confocal raman
Twenty-eight-day Curiochip HLO viability. (A) <t>HLOs</t> were plated <t>on</t> <t>Curiochips,</t> and output media was periodically assessed for albumin secretion (n = 16). (B) CYP450 gene expression was quantified from parallel time points after cell lysis (n = 3). Data were compared to day 14 Curiochips. (C) Day 7 Curiochip cultures were assessed for metabolic function by quantifying molecular turnover of acetaminophen (APAP) and darunavir (DRV) exclusively metabolized by CYP450s using LC/MS/MS; n = 3 and 16 for HLO and Curiochips, respectively. Data are expressed as mean ± standard error of the mean. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.
Cryogenic Nsom/Afm/Confocal Raman, supplied by Nanonics Imaging 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/confocal+imaging/10__1557_slash_mrs2008__206-495-17-6?v=Nanonics+Imaging+Ltd
Average 90 stars, based on 1 article reviews
cryogenic nsom/afm/confocal raman - by Bioz Stars, 2026-08
90/100 stars
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90
Hamamatsu ultraview confocal imaging system 9100 emccd
Twenty-eight-day Curiochip HLO viability. (A) <t>HLOs</t> were plated <t>on</t> <t>Curiochips,</t> and output media was periodically assessed for albumin secretion (n = 16). (B) CYP450 gene expression was quantified from parallel time points after cell lysis (n = 3). Data were compared to day 14 Curiochips. (C) Day 7 Curiochip cultures were assessed for metabolic function by quantifying molecular turnover of acetaminophen (APAP) and darunavir (DRV) exclusively metabolized by CYP450s using LC/MS/MS; n = 3 and 16 for HLO and Curiochips, respectively. Data are expressed as mean ± standard error of the mean. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.
Ultraview Confocal Imaging System 9100 Emccd, supplied by Hamamatsu, 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/confocal+imaging/pm22234700-89-28-34?v=Hamamatsu
Average 90 stars, based on 1 article reviews
ultraview confocal imaging system 9100 emccd - by Bioz Stars, 2026-08
90/100 stars
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90
Becton Dickinson carv ii confocal
Twenty-eight-day Curiochip HLO viability. (A) <t>HLOs</t> were plated <t>on</t> <t>Curiochips,</t> and output media was periodically assessed for albumin secretion (n = 16). (B) CYP450 gene expression was quantified from parallel time points after cell lysis (n = 3). Data were compared to day 14 Curiochips. (C) Day 7 Curiochip cultures were assessed for metabolic function by quantifying molecular turnover of acetaminophen (APAP) and darunavir (DRV) exclusively metabolized by CYP450s using LC/MS/MS; n = 3 and 16 for HLO and Curiochips, respectively. Data are expressed as mean ± standard error of the mean. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.
Carv Ii Confocal, supplied by Becton Dickinson, 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/confocal+imaging/pmc03749305-210-6-9?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
carv ii confocal - by Bioz Stars, 2026-08
90/100 stars
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90
3i - Intelligent Imaging spinning disk confocal microscope
Twenty-eight-day Curiochip HLO viability. (A) <t>HLOs</t> were plated <t>on</t> <t>Curiochips,</t> and output media was periodically assessed for albumin secretion (n = 16). (B) CYP450 gene expression was quantified from parallel time points after cell lysis (n = 3). Data were compared to day 14 Curiochips. (C) Day 7 Curiochip cultures were assessed for metabolic function by quantifying molecular turnover of acetaminophen (APAP) and darunavir (DRV) exclusively metabolized by CYP450s using LC/MS/MS; n = 3 and 16 for HLO and Curiochips, respectively. Data are expressed as mean ± standard error of the mean. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.
Spinning Disk Confocal Microscope, supplied by 3i - Intelligent Imaging, 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/confocal+imaging/pm39632796-72-6-13?v=3i+-+Intelligent+Imaging
Average 90 stars, based on 1 article reviews
spinning disk confocal microscope - by Bioz Stars, 2026-08
90/100 stars
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90
3i - Intelligent Imaging marianas sdc real time 3d confocal-tirf microscope
Twenty-eight-day Curiochip HLO viability. (A) <t>HLOs</t> were plated <t>on</t> <t>Curiochips,</t> and output media was periodically assessed for albumin secretion (n = 16). (B) CYP450 gene expression was quantified from parallel time points after cell lysis (n = 3). Data were compared to day 14 Curiochips. (C) Day 7 Curiochip cultures were assessed for metabolic function by quantifying molecular turnover of acetaminophen (APAP) and darunavir (DRV) exclusively metabolized by CYP450s using LC/MS/MS; n = 3 and 16 for HLO and Curiochips, respectively. Data are expressed as mean ± standard error of the mean. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.
Marianas Sdc Real Time 3d Confocal Tirf Microscope, supplied by 3i - Intelligent Imaging, 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/confocal+imaging/pmc03277121-217-10-17?v=3i+-+Intelligent+Imaging
Average 90 stars, based on 1 article reviews
marianas sdc real time 3d confocal-tirf microscope - by Bioz Stars, 2026-08
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Image Search Results


Twenty-eight-day Curiochip HLO viability. (A) HLOs were plated on Curiochips, and output media was periodically assessed for albumin secretion (n = 16). (B) CYP450 gene expression was quantified from parallel time points after cell lysis (n = 3). Data were compared to day 14 Curiochips. (C) Day 7 Curiochip cultures were assessed for metabolic function by quantifying molecular turnover of acetaminophen (APAP) and darunavir (DRV) exclusively metabolized by CYP450s using LC/MS/MS; n = 3 and 16 for HLO and Curiochips, respectively. Data are expressed as mean ± standard error of the mean. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.

Journal: Gastro Hep Advances

Article Title: A High-Throughput Microphysiological Liver Chip System to Model Drug-Induced Liver Injury Using Human Liver Organoids

doi: 10.1016/j.gastha.2024.08.004

Figure Lengend Snippet: Twenty-eight-day Curiochip HLO viability. (A) HLOs were plated on Curiochips, and output media was periodically assessed for albumin secretion (n = 16). (B) CYP450 gene expression was quantified from parallel time points after cell lysis (n = 3). Data were compared to day 14 Curiochips. (C) Day 7 Curiochip cultures were assessed for metabolic function by quantifying molecular turnover of acetaminophen (APAP) and darunavir (DRV) exclusively metabolized by CYP450s using LC/MS/MS; n = 3 and 16 for HLO and Curiochips, respectively. Data are expressed as mean ± standard error of the mean. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.

Article Snippet: In situ differentiation of HLOs on Curiochips. (A) Confocal fluorescence imaging of HLOs differentiated directly on Curiochips with cell-specific staining of hepatocytes (CEBPA) and hepatic stellate cells (vimentin). (B) Kinetic albumin secretion from in situ and ex situ differentiation of HLOs (n = 16).

Techniques: Gene Expression, Lysis, Liquid Chromatography with Mass Spectroscopy

Functional and phenotypic assessment of Curiochips as a long-term DILI model. (A) Schematic drawing of chronic DILI assay using HLOs on Curiochips. Curiochips were treated for 7 days with either (B) APAP or (C) FIAU and assessed for kinetic hepatocyte function and injury through biochemical analysis of albumin secretion and ALT activity. Multiple comparisons were made between sequential drug treatment time points. (D) Fluorescent images of vehicle control and drug-treated Curiochips stained for DNA and neutral lipid droplets were (E) quantified for total lipid intensity. Data are expressed as mean ± SEM of n = 16 Curiochips per treatment group. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.

Journal: Gastro Hep Advances

Article Title: A High-Throughput Microphysiological Liver Chip System to Model Drug-Induced Liver Injury Using Human Liver Organoids

doi: 10.1016/j.gastha.2024.08.004

Figure Lengend Snippet: Functional and phenotypic assessment of Curiochips as a long-term DILI model. (A) Schematic drawing of chronic DILI assay using HLOs on Curiochips. Curiochips were treated for 7 days with either (B) APAP or (C) FIAU and assessed for kinetic hepatocyte function and injury through biochemical analysis of albumin secretion and ALT activity. Multiple comparisons were made between sequential drug treatment time points. (D) Fluorescent images of vehicle control and drug-treated Curiochips stained for DNA and neutral lipid droplets were (E) quantified for total lipid intensity. Data are expressed as mean ± SEM of n = 16 Curiochips per treatment group. ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.

Article Snippet: In situ differentiation of HLOs on Curiochips. (A) Confocal fluorescence imaging of HLOs differentiated directly on Curiochips with cell-specific staining of hepatocytes (CEBPA) and hepatic stellate cells (vimentin). (B) Kinetic albumin secretion from in situ and ex situ differentiation of HLOs (n = 16).

Techniques: Functional Assay, Activity Assay, Control, Staining

In situ differentiation of HLOs on Curiochips. (A) Confocal fluorescence imaging of HLOs differentiated directly on Curiochips with cell-specific staining of hepatocytes (CEBPA) and hepatic stellate cells (vimentin). (B) Kinetic albumin secretion from in situ and ex situ differentiation of HLOs (n = 16). Multiple comparisons were made between sequential days of culture. The yellow dotted line represents the date of complete HLO differentiation (corresponds to day 0 in <xref ref-type=Figure 2 ). (C) CYP450 gene expression (n = 3) from in situ differentiated Curiochips compared to ex situ differentiation, both at day 21 of differentiation. DILI model evaluation of in situ Curiochips was quantified by ALT activity after (D) APAP and (E) FIAU treatments, over (n = 16 for each condition). Data are expressed as mean ± SEM; ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant. " width="100%" height="100%">

Journal: Gastro Hep Advances

Article Title: A High-Throughput Microphysiological Liver Chip System to Model Drug-Induced Liver Injury Using Human Liver Organoids

doi: 10.1016/j.gastha.2024.08.004

Figure Lengend Snippet: In situ differentiation of HLOs on Curiochips. (A) Confocal fluorescence imaging of HLOs differentiated directly on Curiochips with cell-specific staining of hepatocytes (CEBPA) and hepatic stellate cells (vimentin). (B) Kinetic albumin secretion from in situ and ex situ differentiation of HLOs (n = 16). Multiple comparisons were made between sequential days of culture. The yellow dotted line represents the date of complete HLO differentiation (corresponds to day 0 in Figure 2 ). (C) CYP450 gene expression (n = 3) from in situ differentiated Curiochips compared to ex situ differentiation, both at day 21 of differentiation. DILI model evaluation of in situ Curiochips was quantified by ALT activity after (D) APAP and (E) FIAU treatments, over (n = 16 for each condition). Data are expressed as mean ± SEM; ∗ P < .05; ∗∗ P < .01; ∗∗∗ P < .001; ∗∗∗∗ P < .0001; n.s., not significant.

Article Snippet: In situ differentiation of HLOs on Curiochips. (A) Confocal fluorescence imaging of HLOs differentiated directly on Curiochips with cell-specific staining of hepatocytes (CEBPA) and hepatic stellate cells (vimentin). (B) Kinetic albumin secretion from in situ and ex situ differentiation of HLOs (n = 16).

Techniques: In Situ, Fluorescence, Imaging, Staining, Ex Situ, Gene Expression, Activity Assay