eclipse te2000–s c1si laser scanning confocal microscope Search Results


confocal laser scanning microscopy clsm  (Nikon)
99
Nikon confocal laser scanning microscopy clsm
Fig. 3 Study on cytotoxicity and 1O2 generation in vitro. a Mean fluorescence intensity (MFI) values of [Ru(dpp)3]Cl2 in cells. b Intracellular ROS detection with 660 nm irradiation under hypoxia by flow analysis. c <t>CLSM</t> images of intracellular hypoxia levels under 1% O2 with different treatments (blue, fluorescence of Hoechst 33342; red, fluorescence of ROS-ID hypoxia probe; overlay images). d Under hypoxia, viability of CT26 cells incubated with 660 nm irradiation. e Under normoxia, relative CT26 cell viabilities (PB 18 mg L−1, PCN 9 mg L−1). f Western blot demonstrating the HIF-α level and g the HSP level after various treatments (+ indicates the addition of 660 nm irradiation; HPB@PCN indicates the high concentration of PB@PCN). (Results are expressed as the mean ± SD of at least three independent experiments measured in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001. Scale bar: 40 μm)
Confocal Laser Scanning Microscopy Clsm, 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+te2000%E2%80%93s+c1si+laser+scanning+confocal+microscope/10__1038_slash_s41427___019___0164___4-46-9-14?v=Nikon
Average 99 stars, based on 1 article reviews
confocal laser scanning microscopy clsm - by Bioz Stars, 2026-08
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eclipse te2000 s c1si laser scanning confocal microscope  (Nikon)
99
Nikon eclipse te2000 s c1si laser scanning confocal microscope
Fig. 3 Study on cytotoxicity and 1O2 generation in vitro. a Mean fluorescence intensity (MFI) values of [Ru(dpp)3]Cl2 in cells. b Intracellular ROS detection with 660 nm irradiation under hypoxia by flow analysis. c <t>CLSM</t> images of intracellular hypoxia levels under 1% O2 with different treatments (blue, fluorescence of Hoechst 33342; red, fluorescence of ROS-ID hypoxia probe; overlay images). d Under hypoxia, viability of CT26 cells incubated with 660 nm irradiation. e Under normoxia, relative CT26 cell viabilities (PB 18 mg L−1, PCN 9 mg L−1). f Western blot demonstrating the HIF-α level and g the HSP level after various treatments (+ indicates the addition of 660 nm irradiation; HPB@PCN indicates the high concentration of PB@PCN). (Results are expressed as the mean ± SD of at least three independent experiments measured in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001. Scale bar: 40 μm)
Eclipse Te2000 S C1si Laser Scanning Confocal 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+te2000%E2%80%93s+c1si+laser+scanning+confocal+microscope/pm39252643-311-36-35?v=Nikon
Average 99 stars, based on 1 article reviews
eclipse te2000 s c1si laser scanning confocal microscope - by Bioz Stars, 2026-08
99/100 stars
  Buy from Supplier
c1si confocal laser scanning module  (Nikon)
95
Nikon c1si confocal laser scanning module
Fig. 3 Study on cytotoxicity and 1O2 generation in vitro. a Mean fluorescence intensity (MFI) values of [Ru(dpp)3]Cl2 in cells. b Intracellular ROS detection with 660 nm irradiation under hypoxia by flow analysis. c <t>CLSM</t> images of intracellular hypoxia levels under 1% O2 with different treatments (blue, fluorescence of Hoechst 33342; red, fluorescence of ROS-ID hypoxia probe; overlay images). d Under hypoxia, viability of CT26 cells incubated with 660 nm irradiation. e Under normoxia, relative CT26 cell viabilities (PB 18 mg L−1, PCN 9 mg L−1). f Western blot demonstrating the HIF-α level and g the HSP level after various treatments (+ indicates the addition of 660 nm irradiation; HPB@PCN indicates the high concentration of PB@PCN). (Results are expressed as the mean ± SD of at least three independent experiments measured in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001. Scale bar: 40 μm)
C1si Confocal Laser Scanning Module, supplied by Nikon, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/eclipse+te2000%E2%80%93s+c1si+laser+scanning+confocal+microscope/pm18341554-75-104-103?v=Nikon
Average 95 stars, based on 1 article reviews
c1si confocal laser scanning module - by Bioz Stars, 2026-08
95/100 stars
  Buy from Supplier

Image Search Results


Fig. 3 Study on cytotoxicity and 1O2 generation in vitro. a Mean fluorescence intensity (MFI) values of [Ru(dpp)3]Cl2 in cells. b Intracellular ROS detection with 660 nm irradiation under hypoxia by flow analysis. c CLSM images of intracellular hypoxia levels under 1% O2 with different treatments (blue, fluorescence of Hoechst 33342; red, fluorescence of ROS-ID hypoxia probe; overlay images). d Under hypoxia, viability of CT26 cells incubated with 660 nm irradiation. e Under normoxia, relative CT26 cell viabilities (PB 18 mg L−1, PCN 9 mg L−1). f Western blot demonstrating the HIF-α level and g the HSP level after various treatments (+ indicates the addition of 660 nm irradiation; HPB@PCN indicates the high concentration of PB@PCN). (Results are expressed as the mean ± SD of at least three independent experiments measured in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001. Scale bar: 40 μm)

Journal: NPG Asia Materials

Article Title: Controlled synthesis of a core-shell nanohybrid for effective multimodal image-guided combined photothermal/photodynamic therapy of tumors

doi: 10.1038/s41427-019-0164-4

Figure Lengend Snippet: Fig. 3 Study on cytotoxicity and 1O2 generation in vitro. a Mean fluorescence intensity (MFI) values of [Ru(dpp)3]Cl2 in cells. b Intracellular ROS detection with 660 nm irradiation under hypoxia by flow analysis. c CLSM images of intracellular hypoxia levels under 1% O2 with different treatments (blue, fluorescence of Hoechst 33342; red, fluorescence of ROS-ID hypoxia probe; overlay images). d Under hypoxia, viability of CT26 cells incubated with 660 nm irradiation. e Under normoxia, relative CT26 cell viabilities (PB 18 mg L−1, PCN 9 mg L−1). f Western blot demonstrating the HIF-α level and g the HSP level after various treatments (+ indicates the addition of 660 nm irradiation; HPB@PCN indicates the high concentration of PB@PCN). (Results are expressed as the mean ± SD of at least three independent experiments measured in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001. Scale bar: 40 μm)

Article Snippet: All confocal laser microscopy images were collected by a confocal laser scanning microscopy (CLSM) (Nikon C1-Si TE2000, Japan).

Techniques: In Vitro, Irradiation, Incubation, Western Blot, Concentration Assay

Fig. 4 Homotypic target and immune escape of PB@PCN@MEM. a Flow cytometry analysis of CT26, RAW 264.7 and 3T3 cells endocytosis and b corresponding mean fluorescence intensity analysis. (n = 3). c CLSM images of CT26 and 3T3 cells endocytosis. d MTT analysis. e Pharmacokinetic profiles after i.v. injection with PB@PCN and PB@PCN@MEM

Journal: NPG Asia Materials

Article Title: Controlled synthesis of a core-shell nanohybrid for effective multimodal image-guided combined photothermal/photodynamic therapy of tumors

doi: 10.1038/s41427-019-0164-4

Figure Lengend Snippet: Fig. 4 Homotypic target and immune escape of PB@PCN@MEM. a Flow cytometry analysis of CT26, RAW 264.7 and 3T3 cells endocytosis and b corresponding mean fluorescence intensity analysis. (n = 3). c CLSM images of CT26 and 3T3 cells endocytosis. d MTT analysis. e Pharmacokinetic profiles after i.v. injection with PB@PCN and PB@PCN@MEM

Article Snippet: All confocal laser microscopy images were collected by a confocal laser scanning microscopy (CLSM) (Nikon C1-Si TE2000, Japan).

Techniques: Flow Cytometry, Injection