ix83 microscope Search Results


ix83 microscope body  (Olympus)
97
Olympus ix83 microscope body
Ix83 Microscope Body, supplied by Olympus, 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/ix83+microscope/pmc11420169__pnas__2412241121__sapp-59-7-10?v=Olympus
Average 97 stars, based on 1 article reviews
ix83 microscope body - by Bioz Stars, 2026-07
97/100 stars
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nikon ix83 inverted microscope  (Nikon)
99
Nikon nikon ix83 inverted microscope
Nikon Ix83 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/ix83+microscope/bio_rxiv__2024__10__16__618394-266-12-12?v=Nikon
Average 99 stars, based on 1 article reviews
nikon ix83 inverted microscope - by Bioz Stars, 2026-07
99/100 stars
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olympus ix83 microscope  (Boston Industries Inc)
90
Boston Industries Inc olympus ix83 microscope
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Olympus Ix83 Microscope, supplied by Boston Industries 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/ix83+microscope/pmc10349585-226-5-8?v=Boston+Industries+Inc
Average 90 stars, based on 1 article reviews
olympus ix83 microscope - by Bioz Stars, 2026-07
90/100 stars
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ix83 microscope  (Ludl Electronic)
90
Ludl Electronic ix83 microscope
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Ix83 Microscope, supplied by Ludl Electronic, 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/ix83+microscope/bio_rxiv__2021__01__18__427063-193-3-17?v=Ludl+Electronic
Average 90 stars, based on 1 article reviews
ix83 microscope - by Bioz Stars, 2026-07
90/100 stars
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ix83 inverted microscope  (KeyMed Ltd)
90
KeyMed Ltd ix83 inverted microscope
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Ix83 Inverted Microscope, supplied by KeyMed 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/ix83+microscope/pmc10628266-545-9-12?v=KeyMed+Ltd
Average 90 stars, based on 1 article reviews
ix83 inverted microscope - by Bioz Stars, 2026-07
90/100 stars
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ix83 microscope  (TOPTICA Photonics)
90
TOPTICA Photonics ix83 microscope
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Ix83 Microscope, supplied by TOPTICA Photonics, 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/ix83+microscope/pm32672938-214-6-15?v=TOPTICA+Photonics
Average 90 stars, based on 1 article reviews
ix83 microscope - by Bioz Stars, 2026-07
90/100 stars
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ix-83-fv1200 laserscanning confocal microscope  (Laserscanning Europe GmbH)
90
Laserscanning Europe GmbH ix-83-fv1200 laserscanning confocal microscope
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Ix 83 Fv1200 Laserscanning Confocal Microscope, supplied by Laserscanning Europe GmbH, 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/ix83+microscope/pm34113976-121-5-6?v=Laserscanning+Europe+GmbH
Average 90 stars, based on 1 article reviews
ix-83-fv1200 laserscanning confocal microscope - by Bioz Stars, 2026-07
90/100 stars
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ix83 inverted microscope  (ABBELIGHT)
90
ABBELIGHT ix83 inverted microscope
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Ix83 Inverted Microscope, supplied by ABBELIGHT, 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/ix83+microscope/pm37579750-141-17-11?v=ABBELIGHT
Average 90 stars, based on 1 article reviews
ix83 inverted microscope - by Bioz Stars, 2026-07
90/100 stars
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ix83 microscope body  (Visitech Inc)
86
Visitech Inc ix83 microscope body
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Ix83 Microscope Body, supplied by Visitech Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ix83+microscope/pm41831447-188-11-6?v=Visitech+Inc
Average 86 stars, based on 1 article reviews
ix83 microscope body - by Bioz Stars, 2026-07
86/100 stars
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ix83 inverted microscope system  (Olympus)
86
Olympus ix83 inverted microscope system
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Ix83 Inverted Microscope System, supplied by Olympus, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ix83+microscope/pmc12895556-42-1-0?v=Olympus
Average 86 stars, based on 1 article reviews
ix83 inverted microscope system - by Bioz Stars, 2026-07
86/100 stars
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fv1200 ix83 laser scanning confocal microscope  (Olympus)
86
Olympus fv1200 ix83 laser scanning confocal microscope
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Fv1200 Ix83 Laser Scanning Confocal Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ix83+microscope/pm41941983-96-11-10?v=Olympus
Average 86 stars, based on 1 article reviews
fv1200 ix83 laser scanning confocal microscope - by Bioz Stars, 2026-07
86/100 stars
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custom olympus ix83 zdc2 microscope  (Olympus)
86
Olympus custom olympus ix83 zdc2 microscope
The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus <t>IX83</t> <t>microscope</t> (Boston Industries, Inc., MA, USA).
Custom Olympus Ix83 Zdc2 Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ix83+microscope/pm41744790-220-8-9?v=Olympus
Average 86 stars, based on 1 article reviews
custom olympus ix83 zdc2 microscope - by Bioz Stars, 2026-07
86/100 stars
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Image Search Results


The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Journal: International Journal of Nanomedicine

Article Title: Methodological and Cellular Factors Affecting the Magnitude of Breast Cancer and Normal Cell Radiosensitization Using Gold Nanoparticles

doi: 10.2147/IJN.S412458

Figure Lengend Snippet: The mitochondrial membrane potential (JC-1) after the incubation of MDA-MB-231 cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MDA-MB-231 cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Article Snippet: Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Techniques: Membrane, Incubation, Control, Immunofluorescence, Microscopy

The mitochondrial membrane potential (JC-1) after the incubation of MCF12A cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm , and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MCF12A cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Journal: International Journal of Nanomedicine

Article Title: Methodological and Cellular Factors Affecting the Magnitude of Breast Cancer and Normal Cell Radiosensitization Using Gold Nanoparticles

doi: 10.2147/IJN.S412458

Figure Lengend Snippet: The mitochondrial membrane potential (JC-1) after the incubation of MCF12A cells with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm , and RGD-PEG 2000 -AuNPs 30nm . In living cells, the JC-1 dye is absorbed into active mitochondria, where it forms aggregates with fluorescent properties. JC-1 monomers fluoresce under green light (530nm light emission) and JC-1 aggregates fluoresce under red light (595nm light emission). In apoptotic or damaged cells with a low potential of the mitochondrial membrane, JC-1 does not form aggregates, it remains in the form of green fluorescent monomers. The JC-1 level was checked every 5 min till 30 min ( A ). The control group (CTR) was TP of 0 min ( B ). The immunofluorescence JC-1 images were taken after 5, 15 and 25 min of the incubation with AuNPs. The MCF12A cells were photographed after the 5 min ( C ), 15 min ( D ) and 25 min ( E ) incubation with RGD-PEG 800 -AuNPs 10nm , after the 5 min ( F ), 15 min ( G ) and 25 min ( H ) incubation with RGD-PEG 2000 -AuNPs 10nm , after the 5 min ( I ), 15 min ( J ) and 25 min ( K ) incubation with RGD-PEG 800 -AuNPs 30nm , after the 5 min ( L ), 15 min ( M ) and 25 min ( N ) incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Article Snippet: Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Techniques: Membrane, Incubation, Control, Immunofluorescence, Microscopy

Immunofluorescence of MDA-MB-231 cells after irradiation and previous incubation with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . The concentration of AuNPs was 0.0004 mg/mL. Three different TPs of the cells incubation with AuNPs before irradiation were used (30 min, 3 and 24 h). Cells after being exposed to AuNPs and irradiated, were analyzed using immunofluorescence to detect γH2AX (red color) and P53 foci (green color). The nuclei of cells were dyed with DAPI solution (blue color). The control group was not exposed to AuNPs and IR ( A – C ). To compare the effect of AuNPs added before IR, the group of cells exposed only to 2 Gy was presented ( D – F ). Images show obtained results of MDA-MB-231 cells after exposition of 2 Gy and: the 30 min ( G ), 3 h ( H ), 24 h ( I ) previous incubation with RGD-PEG 800 -AuNPs 10nm ; the 30 min ( J ), 3 h ( K ), 24 h ( L ) previous incubation with RGD-PEG 2000 -AuNPs 10nm ; the 30 min ( M ), 3 h ( N ), 24 h ( O ) previous incubation with RGD-PEG 800 -AuNPs 30nm and the 30 min ( P ), 3 h ( R ), 24 h ( S ) previous incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Journal: International Journal of Nanomedicine

Article Title: Methodological and Cellular Factors Affecting the Magnitude of Breast Cancer and Normal Cell Radiosensitization Using Gold Nanoparticles

doi: 10.2147/IJN.S412458

Figure Lengend Snippet: Immunofluorescence of MDA-MB-231 cells after irradiation and previous incubation with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . The concentration of AuNPs was 0.0004 mg/mL. Three different TPs of the cells incubation with AuNPs before irradiation were used (30 min, 3 and 24 h). Cells after being exposed to AuNPs and irradiated, were analyzed using immunofluorescence to detect γH2AX (red color) and P53 foci (green color). The nuclei of cells were dyed with DAPI solution (blue color). The control group was not exposed to AuNPs and IR ( A – C ). To compare the effect of AuNPs added before IR, the group of cells exposed only to 2 Gy was presented ( D – F ). Images show obtained results of MDA-MB-231 cells after exposition of 2 Gy and: the 30 min ( G ), 3 h ( H ), 24 h ( I ) previous incubation with RGD-PEG 800 -AuNPs 10nm ; the 30 min ( J ), 3 h ( K ), 24 h ( L ) previous incubation with RGD-PEG 2000 -AuNPs 10nm ; the 30 min ( M ), 3 h ( N ), 24 h ( O ) previous incubation with RGD-PEG 800 -AuNPs 30nm and the 30 min ( P ), 3 h ( R ), 24 h ( S ) previous incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Article Snippet: Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Techniques: Immunofluorescence, Irradiation, Incubation, Concentration Assay, Control, Microscopy

Immunofluorescence of MCF12A cells after irradiation and previous incubation with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . The concentration of AuNPs was 0.0004 mg/mL. Three different TPs of the cells incubation with AuNPs before irradiation were used (30 min, 3 and 24 h). Cells after exposition to AuNPs and IR were analyzed using immunofluorescence to detect γH2AX (red color) and P53 foci (green color). The nuclei of cells were dyed with DAPI solution (blue color). The control group was not exposed to AuNPs and IR ( A – C ). To compare the effect of AuNPs added before IR, the group of cells exposed only to 2 Gy was presented ( D – F ). Images show obtained results of MCF12A cells after exposition of 2 Gy and: the 30 min ( G ), 3 h ( H ), 24 h ( I ) previous incubation with RGD-PEG 800 -AuNPs 10nm ; the 30 min ( J ), 3 h ( K ), 24 h ( L ) previous incubation with RGD-PEG 2000 -AuNPs 10nm ; the 30 min ( M ), 3 h ( N ), 24 h ( O ) previous incubation with RGD-PEG 800 -AuNPs 30nm and the 30 min ( P ), 3 h ( R ), 24 h ( S ) previous incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Journal: International Journal of Nanomedicine

Article Title: Methodological and Cellular Factors Affecting the Magnitude of Breast Cancer and Normal Cell Radiosensitization Using Gold Nanoparticles

doi: 10.2147/IJN.S412458

Figure Lengend Snippet: Immunofluorescence of MCF12A cells after irradiation and previous incubation with RGD-PEG 800 -AuNPs 10nm , RGD-PEG 2000 -AuNPs 10nm , RGD-PEG 800 -AuNPs 30nm and RGD-PEG 2000 -AuNPs 30nm . The concentration of AuNPs was 0.0004 mg/mL. Three different TPs of the cells incubation with AuNPs before irradiation were used (30 min, 3 and 24 h). Cells after exposition to AuNPs and IR were analyzed using immunofluorescence to detect γH2AX (red color) and P53 foci (green color). The nuclei of cells were dyed with DAPI solution (blue color). The control group was not exposed to AuNPs and IR ( A – C ). To compare the effect of AuNPs added before IR, the group of cells exposed only to 2 Gy was presented ( D – F ). Images show obtained results of MCF12A cells after exposition of 2 Gy and: the 30 min ( G ), 3 h ( H ), 24 h ( I ) previous incubation with RGD-PEG 800 -AuNPs 10nm ; the 30 min ( J ), 3 h ( K ), 24 h ( L ) previous incubation with RGD-PEG 2000 -AuNPs 10nm ; the 30 min ( M ), 3 h ( N ), 24 h ( O ) previous incubation with RGD-PEG 800 -AuNPs 30nm and the 30 min ( P ), 3 h ( R ), 24 h ( S ) previous incubation with RGD-PEG 2000 -AuNPs 30nm . Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Article Snippet: Immunofluorescence was photographed using a Olympus IX83 microscope (Boston Industries, Inc., MA, USA).

Techniques: Immunofluorescence, Irradiation, Incubation, Concentration Assay, Control, Microscopy