az-100 multizoom macroscope Search Results


az100 multizoom macroscope  (Nikon)
99
Nikon az100 multizoom macroscope
Az100 Multizoom Macroscope, 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/az-100+multizoom+macroscope/Objectives/bio_rxiv__815191-85-17-29
Average 99 stars, based on 1 article reviews
az100 multizoom macroscope - by Bioz Stars, 2026-09
99/100 stars
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fluorescence zoom microscope  (Nikon)
96
Nikon fluorescence zoom microscope
Inoculation of human cancer cells into immunodeficient mice and in vivo macroscopic imaging using a <t>fluorescence</t> zoom <t>microscope.</t> (a) Schema of the sites of inoculation of human cancer cells. The cells were inoculated s.c. into the back skin of nude mice at the rostral–ventral site (HT1080-GFP cells), the caudal–ventral site (HT1080-GFP-CEA cells) or the dorsal site (MKN45-GFP cells). (b) Schema of preparation of skin flaps. Seven or eight days after the inoculation, the inoculation sites were exposed by the skin-flap method. (c–e) In vivo macro imaging of tumors. In vivo macro imaging of the tumor masses was performed using a fluorescence zoom microscope 24 h after injection of Alexa Fluor 594-conjugated anti-CEA antibody (50 μg/mouse). Exposure times for the GFP and Alexa Fluor 594 fluorescence images were 30 and 100 ms, respectively. These experiments were repeated three times and similar results were obtained.
Fluorescence Zoom 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/az-100+multizoom+macroscope/Fluorescence+Filter+Cubes/pmc04462348-40-8-13
Average 96 stars, based on 1 article reviews
fluorescence zoom microscope - by Bioz Stars, 2026-09
96/100 stars
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130w metal halide lamp white source  (Nikon)
96
Nikon 130w metal halide lamp white source
Inoculation of human cancer cells into immunodeficient mice and in vivo macroscopic imaging using a <t>fluorescence</t> zoom <t>microscope.</t> (a) Schema of the sites of inoculation of human cancer cells. The cells were inoculated s.c. into the back skin of nude mice at the rostral–ventral site (HT1080-GFP cells), the caudal–ventral site (HT1080-GFP-CEA cells) or the dorsal site (MKN45-GFP cells). (b) Schema of preparation of skin flaps. Seven or eight days after the inoculation, the inoculation sites were exposed by the skin-flap method. (c–e) In vivo macro imaging of tumors. In vivo macro imaging of the tumor masses was performed using a fluorescence zoom microscope 24 h after injection of Alexa Fluor 594-conjugated anti-CEA antibody (50 μg/mouse). Exposure times for the GFP and Alexa Fluor 594 fluorescence images were 30 and 100 ms, respectively. These experiments were repeated three times and similar results were obtained.
130w Metal Halide Lamp White Source, 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/az-100+multizoom+macroscope/Intensilight/pmc03528039-53-14-21
Average 96 stars, based on 1 article reviews
130w metal halide lamp white source - by Bioz Stars, 2026-09
96/100 stars
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pe-300 ultra-light source  (CoolLED Inc)
90
CoolLED Inc pe-300 ultra-light source
Inoculation of human cancer cells into immunodeficient mice and in vivo macroscopic imaging using a <t>fluorescence</t> zoom <t>microscope.</t> (a) Schema of the sites of inoculation of human cancer cells. The cells were inoculated s.c. into the back skin of nude mice at the rostral–ventral site (HT1080-GFP cells), the caudal–ventral site (HT1080-GFP-CEA cells) or the dorsal site (MKN45-GFP cells). (b) Schema of preparation of skin flaps. Seven or eight days after the inoculation, the inoculation sites were exposed by the skin-flap method. (c–e) In vivo macro imaging of tumors. In vivo macro imaging of the tumor masses was performed using a fluorescence zoom microscope 24 h after injection of Alexa Fluor 594-conjugated anti-CEA antibody (50 μg/mouse). Exposure times for the GFP and Alexa Fluor 594 fluorescence images were 30 and 100 ms, respectively. These experiments were repeated three times and similar results were obtained.
Pe 300 Ultra Light Source, supplied by CoolLED 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/az-100+multizoom+macroscope/pe+300/pmc09631707-52-35-35
Average 90 stars, based on 1 article reviews
pe-300 ultra-light source - by Bioz Stars, 2026-09
90/100 stars
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nikon nis elements ar software  (Nikon)
99
Nikon nikon nis elements ar software
Inoculation of human cancer cells into immunodeficient mice and in vivo macroscopic imaging using a <t>fluorescence</t> zoom <t>microscope.</t> (a) Schema of the sites of inoculation of human cancer cells. The cells were inoculated s.c. into the back skin of nude mice at the rostral–ventral site (HT1080-GFP cells), the caudal–ventral site (HT1080-GFP-CEA cells) or the dorsal site (MKN45-GFP cells). (b) Schema of preparation of skin flaps. Seven or eight days after the inoculation, the inoculation sites were exposed by the skin-flap method. (c–e) In vivo macro imaging of tumors. In vivo macro imaging of the tumor masses was performed using a fluorescence zoom microscope 24 h after injection of Alexa Fluor 594-conjugated anti-CEA antibody (50 μg/mouse). Exposure times for the GFP and Alexa Fluor 594 fluorescence images were 30 and 100 ms, respectively. These experiments were repeated three times and similar results were obtained.
Nikon Nis Elements Ar 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/az-100+multizoom+macroscope/NIS-Elements/pm35767737-85-65-71
Average 99 stars, based on 1 article reviews
nikon nis elements ar software - by Bioz Stars, 2026-09
99/100 stars
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brightline led-da/ fi/tr/cy5-4x-b-nte filter set  (IDEX)
90
IDEX brightline led-da/ fi/tr/cy5-4x-b-nte filter set
Inoculation of human cancer cells into immunodeficient mice and in vivo macroscopic imaging using a <t>fluorescence</t> zoom <t>microscope.</t> (a) Schema of the sites of inoculation of human cancer cells. The cells were inoculated s.c. into the back skin of nude mice at the rostral–ventral site (HT1080-GFP cells), the caudal–ventral site (HT1080-GFP-CEA cells) or the dorsal site (MKN45-GFP cells). (b) Schema of preparation of skin flaps. Seven or eight days after the inoculation, the inoculation sites were exposed by the skin-flap method. (c–e) In vivo macro imaging of tumors. In vivo macro imaging of the tumor masses was performed using a fluorescence zoom microscope 24 h after injection of Alexa Fluor 594-conjugated anti-CEA antibody (50 μg/mouse). Exposure times for the GFP and Alexa Fluor 594 fluorescence images were 30 and 100 ms, respectively. These experiments were repeated three times and similar results were obtained.
Brightline Led Da/ Fi/Tr/Cy5 4x B Nte Filter Set, supplied by IDEX, 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/az-100+multizoom+macroscope/multiband+dichroic+filter/pm35767737-85-42-47
Average 90 stars, based on 1 article reviews
brightline led-da/ fi/tr/cy5-4x-b-nte filter set - by Bioz Stars, 2026-09
90/100 stars
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andor sona scmos4 2b camera  (Oxford Instruments)
97
Oxford Instruments andor sona scmos4 2b camera
Inoculation of human cancer cells into immunodeficient mice and in vivo macroscopic imaging using a <t>fluorescence</t> zoom <t>microscope.</t> (a) Schema of the sites of inoculation of human cancer cells. The cells were inoculated s.c. into the back skin of nude mice at the rostral–ventral site (HT1080-GFP cells), the caudal–ventral site (HT1080-GFP-CEA cells) or the dorsal site (MKN45-GFP cells). (b) Schema of preparation of skin flaps. Seven or eight days after the inoculation, the inoculation sites were exposed by the skin-flap method. (c–e) In vivo macro imaging of tumors. In vivo macro imaging of the tumor masses was performed using a fluorescence zoom microscope 24 h after injection of Alexa Fluor 594-conjugated anti-CEA antibody (50 μg/mouse). Exposure times for the GFP and Alexa Fluor 594 fluorescence images were 30 and 100 ms, respectively. These experiments were repeated three times and similar results were obtained.
Andor Sona Scmos4 2b Camera, supplied by Oxford Instruments, 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/az-100+multizoom+macroscope/Sona/pm35767737-85-53-58
Average 97 stars, based on 1 article reviews
andor sona scmos4 2b camera - by Bioz Stars, 2026-09
97/100 stars
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Image Search Results


Inoculation of human cancer cells into immunodeficient mice and in vivo macroscopic imaging using a fluorescence zoom microscope. (a) Schema of the sites of inoculation of human cancer cells. The cells were inoculated s.c. into the back skin of nude mice at the rostral–ventral site (HT1080-GFP cells), the caudal–ventral site (HT1080-GFP-CEA cells) or the dorsal site (MKN45-GFP cells). (b) Schema of preparation of skin flaps. Seven or eight days after the inoculation, the inoculation sites were exposed by the skin-flap method. (c–e) In vivo macro imaging of tumors. In vivo macro imaging of the tumor masses was performed using a fluorescence zoom microscope 24 h after injection of Alexa Fluor 594-conjugated anti-CEA antibody (50 μg/mouse). Exposure times for the GFP and Alexa Fluor 594 fluorescence images were 30 and 100 ms, respectively. These experiments were repeated three times and similar results were obtained.

Journal: Cancer Science

Article Title: In vivo subcellular imaging of tumors in mouse models using a fluorophore-conjugated anti-carcinoembryonic antigen antibody in two-photon excitation microscopy

doi: 10.1111/cas.12500

Figure Lengend Snippet: Inoculation of human cancer cells into immunodeficient mice and in vivo macroscopic imaging using a fluorescence zoom microscope. (a) Schema of the sites of inoculation of human cancer cells. The cells were inoculated s.c. into the back skin of nude mice at the rostral–ventral site (HT1080-GFP cells), the caudal–ventral site (HT1080-GFP-CEA cells) or the dorsal site (MKN45-GFP cells). (b) Schema of preparation of skin flaps. Seven or eight days after the inoculation, the inoculation sites were exposed by the skin-flap method. (c–e) In vivo macro imaging of tumors. In vivo macro imaging of the tumor masses was performed using a fluorescence zoom microscope 24 h after injection of Alexa Fluor 594-conjugated anti-CEA antibody (50 μg/mouse). Exposure times for the GFP and Alexa Fluor 594 fluorescence images were 30 and 100 ms, respectively. These experiments were repeated three times and similar results were obtained.

Article Snippet: In vivo macroscopic imaging was performed using a fluorescence zoom microscope (MULTIZOOM AZ100; Nikon) with a GFP-HQ filter set (for GFP) and a Texas Red filter set (for Alexa Fluor 594), and an AZ-Plan Apo 0.5× Plan Fluor objective lens (Nikon).

Techniques: In Vivo, Imaging, Fluorescence, Microscopy, Injection

In vivo fluorescence imaging using a two-photon microscope. After the in vivo macroscopic imaging as shown in Figure (c–e), the same tumors were observed by two-photon excitation microscopy. (a–f) 3-D and 2-D images of HT1080-GFP (a, d), HT1080-GFP-CEA (b, e) and MKN45 (c, f) cells were acquired by two-photon excitation microscopy. Each 2-D image represents an orthogonal view: x-y (center panel), y-z (left panel) and x-z (lower panel). Red, green and blue indicate Alexa Fluor 594 fluorescence, GFP fluorescence and second harmonic generation (SHG), respectively. (g–i) Magnified images of (d–f).

Journal: Cancer Science

Article Title: In vivo subcellular imaging of tumors in mouse models using a fluorophore-conjugated anti-carcinoembryonic antigen antibody in two-photon excitation microscopy

doi: 10.1111/cas.12500

Figure Lengend Snippet: In vivo fluorescence imaging using a two-photon microscope. After the in vivo macroscopic imaging as shown in Figure (c–e), the same tumors were observed by two-photon excitation microscopy. (a–f) 3-D and 2-D images of HT1080-GFP (a, d), HT1080-GFP-CEA (b, e) and MKN45 (c, f) cells were acquired by two-photon excitation microscopy. Each 2-D image represents an orthogonal view: x-y (center panel), y-z (left panel) and x-z (lower panel). Red, green and blue indicate Alexa Fluor 594 fluorescence, GFP fluorescence and second harmonic generation (SHG), respectively. (g–i) Magnified images of (d–f).

Article Snippet: In vivo macroscopic imaging was performed using a fluorescence zoom microscope (MULTIZOOM AZ100; Nikon) with a GFP-HQ filter set (for GFP) and a Texas Red filter set (for Alexa Fluor 594), and an AZ-Plan Apo 0.5× Plan Fluor objective lens (Nikon).

Techniques: In Vivo, Fluorescence, Imaging, Microscopy

In vivo fluorescence macroscopic and microscopic imaging of lymph-node metastases by a fluorescence zoom microscope and a two-photon excitation microscope. (a–c) A footpad spontaneous metastasis model using HT1080-GFP-CEA cells observed by a fluorescence zoom microscope. The popliteal lymph node was exposed, and multiple images were collected: bright field image (a), GFP (b) and Alexa Fluor 594 (c). Exposure times for the GFP and Alexa Fluor 594 images were 1000 and 3000 ms, respectively. (d–f) Two-photon excitation microscopy of the popliteal lymph node. After in vivo macroscopic imaging, the same lymph node was observed using a two-photon excitation microscope. Acquired images are shown as 3-D construction (d), cropped 3-D image of (e) and magnified image of (f), respectively. Red, green and blue indicate Alexa Fluor 594 fluorescence, GFP fluorescence and second harmonic generation (SHG), respectively.

Journal: Cancer Science

Article Title: In vivo subcellular imaging of tumors in mouse models using a fluorophore-conjugated anti-carcinoembryonic antigen antibody in two-photon excitation microscopy

doi: 10.1111/cas.12500

Figure Lengend Snippet: In vivo fluorescence macroscopic and microscopic imaging of lymph-node metastases by a fluorescence zoom microscope and a two-photon excitation microscope. (a–c) A footpad spontaneous metastasis model using HT1080-GFP-CEA cells observed by a fluorescence zoom microscope. The popliteal lymph node was exposed, and multiple images were collected: bright field image (a), GFP (b) and Alexa Fluor 594 (c). Exposure times for the GFP and Alexa Fluor 594 images were 1000 and 3000 ms, respectively. (d–f) Two-photon excitation microscopy of the popliteal lymph node. After in vivo macroscopic imaging, the same lymph node was observed using a two-photon excitation microscope. Acquired images are shown as 3-D construction (d), cropped 3-D image of (e) and magnified image of (f), respectively. Red, green and blue indicate Alexa Fluor 594 fluorescence, GFP fluorescence and second harmonic generation (SHG), respectively.

Article Snippet: In vivo macroscopic imaging was performed using a fluorescence zoom microscope (MULTIZOOM AZ100; Nikon) with a GFP-HQ filter set (for GFP) and a Texas Red filter set (for Alexa Fluor 594), and an AZ-Plan Apo 0.5× Plan Fluor objective lens (Nikon).

Techniques: In Vivo, Fluorescence, Imaging, Microscopy