eclipse ni e fluorescent microscope Search Results


eclipse ni e fluorescent microscope  (Nikon)
96
Nikon eclipse ni e fluorescent microscope
Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse <t>fluorescent</t> <t>microscope</t> up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com
Eclipse Ni E Fluorescent Microscope, supplied by Nikon, 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/eclipse+ni+e+fluorescent+microscope/ECLIPSE+Ni-E%2FNi-U/pmc11538101-83-38-37
Average 96 stars, based on 1 article reviews
eclipse ni e fluorescent microscope - by Bioz Stars, 2026-09
96/100 stars
  Buy from Supplier
fluorescence inverted microscope  (Nikon)
99
Nikon fluorescence inverted microscope
Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse <t>fluorescent</t> <t>microscope</t> up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com
Fluorescence Inverted Microscope, 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/eclipse+ni+e+fluorescent+microscope/Inverted+Microscopes/pm40077620-55-35-38
Average 99 stars, based on 1 article reviews
fluorescence inverted microscope - by Bioz Stars, 2026-09
99/100 stars
  Buy from Supplier
eclipse ni e upright fluorescence microscope  (Nikon)
99
Nikon eclipse ni e upright fluorescence microscope
Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse <t>fluorescent</t> <t>microscope</t> up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com
Eclipse Ni E Upright Fluorescence Microscope, 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/eclipse+ni+e+fluorescent+microscope/Objectives/pmc12863670-72-9-8
Average 99 stars, based on 1 article reviews
eclipse ni e upright fluorescence microscope - by Bioz Stars, 2026-09
99/100 stars
  Buy from Supplier
ds ri2 camera  (Nikon)
99
Nikon ds ri2 camera
Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse <t>fluorescent</t> <t>microscope</t> up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com
Ds Ri2 Camera, 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/eclipse+ni+e+fluorescent+microscope/DS-Ri2/bio_rxiv__2021__08__07__453742-191-13-12
Average 99 stars, based on 1 article reviews
ds ri2 camera - by Bioz Stars, 2026-09
99/100 stars
  Buy from Supplier
fluorescence microscope  (Nikon)
96
Nikon fluorescence microscope
Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse <t>fluorescent</t> <t>microscope</t> up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com
Fluorescence Microscope, supplied by Nikon, 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/eclipse+ni+e+fluorescent+microscope/Fluorescence+Filter+Cubes/pmc12071778-191-6-11
Average 96 stars, based on 1 article reviews
fluorescence microscope - by Bioz Stars, 2026-09
96/100 stars
  Buy from Supplier
nie fluorescent microscope  (Nikon)
99
Nikon nie fluorescent microscope
Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse <t>fluorescent</t> <t>microscope</t> up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com
Nie Fluorescent Microscope, 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/eclipse+ni+e+fluorescent+microscope/NIS-Elements/bio_rxiv__2024__04__18__590133-118-17-16
Average 99 stars, based on 1 article reviews
nie fluorescent microscope - by Bioz Stars, 2026-09
99/100 stars
  Buy from Supplier
a1r confocal microscope  (Nikon)
96
Nikon a1r confocal microscope
Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse <t>fluorescent</t> <t>microscope</t> up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com
A1r Confocal Microscope, supplied by Nikon, 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/eclipse+ni+e+fluorescent+microscope/A1+MP%2B+%2F+A1R+MP%2B/pmc11062917-433-16-15
Average 96 stars, based on 1 article reviews
a1r confocal microscope - by Bioz Stars, 2026-09
96/100 stars
  Buy from Supplier
microscope  (Nikon)
98
Nikon microscope
Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse <t>fluorescent</t> <t>microscope</t> up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com
Microscope, supplied by Nikon, 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/eclipse+ni+e+fluorescent+microscope/SMZ800N/pm35088131-56-8-12
Average 98 stars, based on 1 article reviews
microscope - by Bioz Stars, 2026-09
98/100 stars
  Buy from Supplier
epi fluorescence microscope  (Nikon)
96
Nikon epi fluorescence microscope
Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse <t>fluorescent</t> <t>microscope</t> up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com
Epi Fluorescence Microscope, supplied by Nikon, 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/eclipse+ni+e+fluorescent+microscope/Epi-Fl+LED+Illuminator/pmc08511898-300-23-27
Average 96 stars, based on 1 article reviews
epi fluorescence microscope - by Bioz Stars, 2026-09
96/100 stars
  Buy from Supplier

Image Search Results


Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse fluorescent microscope up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com

Journal: Cellular and Molecular Bioengineering

Article Title: Multicompartmentalized Microvascularized Tumor-on-a-Chip to Study Tumor-Stroma Interactions and Drug Resistance in Ovarian Cancer

doi: 10.1007/s12195-024-00817-y

Figure Lengend Snippet: Microfluidic device mimics drug penetration gradients in OC-TME. a Schematic representation of method used for doxorubicin penetration assay, where doxorubicin (100 µM) was injected in both circulation channels and images were taken in time-lapse fluorescent microscope up to 24 h. b Representative images at 5 min, 30 min, 2, 4, 7 and 24 h of doxorubicin penetration. Scale Bar = 1 mm. c Quantification of the fluid velocity (μm/s) inside the microfluidic device over the time (h) (left) and MFI of doxorubicin penetration inside the cancer and stromal chambers at each time point (right). d Schematic representation of method used for doxorubicin uptake, cancer cells were cultured surrounded by different stromal cells (EC, NF, or CAF) or blank scaffold as a control for 5 days and then doxorubicin (100 µM) was injected in both circulation channels and images were taken at 24 h. e Representative images of doxorubicin uptake by cells at 24 h. Scale Bar = 1 mm. Figure a and d created with Biorender.com

Article Snippet: The images were taken at different time points (0; 0.25; 0.5; 0.75, 1; 1.25; 1.5; 1.75; 2, 2.5; 3; 4; 5; 6; 7; 8; 24 hours) for drug penetration and at 24 h for drug uptake using Nikon Eclipse Ni-E fluorescent microscope (EX 559.5 nm/EM 645 nm) at 10× magnification.

Techniques: Injection, Microscopy, Cell Culture, Control