eclipse ti2 e widefield fluorescence microscope Search Results


99
Nikon ti2 e widefield microscope
Ti2 E Widefield 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+ti2+e+widefield+fluorescence+microscope/us11584792-1821-25-24?v=Nikon
Average 99 stars, based on 1 article reviews
ti2 e widefield microscope - by Bioz Stars, 2026-08
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99
Nikon widefield inverted eclipse ti2 e microscope
Widefield Inverted Eclipse Ti2 E 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+ti2+e+widefield+fluorescence+microscope/bio_rxiv__64898__2026__02__01__703127-247-7-12?v=Nikon
Average 99 stars, based on 1 article reviews
widefield inverted eclipse ti2 e microscope - by Bioz Stars, 2026-08
99/100 stars
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99
Nikon inverted microscope
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+ti2+e+widefield+fluorescence+microscope/pmc08188197__ADVS___8___2003721___s001-182-11-13?v=Nikon
Average 99 stars, based on 1 article reviews
inverted microscope - by Bioz Stars, 2026-08
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96
Carl Zeiss widefield microscope
Widefield Microscope, supplied by Carl Zeiss, 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+ti2+e+widefield+fluorescence+microscope/bio_rxiv__2021__03__07__434278-86-27-31?v=Carl+Zeiss
Average 96 stars, based on 1 article reviews
widefield microscope - by Bioz Stars, 2026-08
96/100 stars
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96
Nikon ti2e fluorescence widefield microscope at 60x
Ti2e Fluorescence Widefield Microscope At 60x, 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+ti2+e+widefield+fluorescence+microscope/bio_rxiv__852194-214-20-19?v=Nikon
Average 96 stars, based on 1 article reviews
ti2e fluorescence widefield microscope at 60x - by Bioz Stars, 2026-08
96/100 stars
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90
Carl Zeiss inverted widefield microscope
(A) Scanning electron microscopy (SEM) images of the fabricated designs’ main variants (“Rams; “Arrows”; “Tesla”). Low magnification images (top) encompass the entire microfluidic device design, while high magnification images (bottom) detail the respective motif design. (B) <t>Widefield</t> microscopy mosaic image (20× objective) of different neuronal populations (“Source” and “Target”) at 14 days in vitro, selectively expressing mRuby3 (red) and EGFP (cyan), cultured on a microfluidic device with the “Tesla” motif. (C) Schematics of the rationale for each motif design. Green, orange and red arrows indicate axonal outgrowth-permissive, re-routing and blocking capabilities, respectively.
Inverted Widefield Microscope, supplied by Carl Zeiss, 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/eclipse+ti2+e+widefield+fluorescence+microscope/bio_rxiv__2024__07__09__602729-160-20-24?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
inverted widefield microscope - by Bioz Stars, 2026-08
90/100 stars
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99
Excelitas corp pco_panda
(A) Scanning electron microscopy (SEM) images of the fabricated designs’ main variants (“Rams; “Arrows”; “Tesla”). Low magnification images (top) encompass the entire microfluidic device design, while high magnification images (bottom) detail the respective motif design. (B) <t>Widefield</t> microscopy mosaic image (20× objective) of different neuronal populations (“Source” and “Target”) at 14 days in vitro, selectively expressing mRuby3 (red) and EGFP (cyan), cultured on a microfluidic device with the “Tesla” motif. (C) Schematics of the rationale for each motif design. Green, orange and red arrows indicate axonal outgrowth-permissive, re-routing and blocking capabilities, respectively.
Pco Panda, supplied by Excelitas corp, 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+ti2+e+widefield+fluorescence+microscope/custom%40pco_panda%4010%2E64898%2F2026%2E05%2E25%2E727761?v=Excelitas+corp
Average 99 stars, based on 1 article reviews
pco_panda - by Bioz Stars, 2026-08
99/100 stars
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86
Lumencor Inc lumencor sola led engine
(A) Scanning electron microscopy (SEM) images of the fabricated designs’ main variants (“Rams; “Arrows”; “Tesla”). Low magnification images (top) encompass the entire microfluidic device design, while high magnification images (bottom) detail the respective motif design. (B) <t>Widefield</t> microscopy mosaic image (20× objective) of different neuronal populations (“Source” and “Target”) at 14 days in vitro, selectively expressing mRuby3 (red) and EGFP (cyan), cultured on a microfluidic device with the “Tesla” motif. (C) Schematics of the rationale for each motif design. Green, orange and red arrows indicate axonal outgrowth-permissive, re-routing and blocking capabilities, respectively.
Lumencor Sola Led Engine, supplied by Lumencor 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/eclipse+ti2+e+widefield+fluorescence+microscope/pm41417753-214-14-14?v=Lumencor+Inc
Average 86 stars, based on 1 article reviews
lumencor sola led engine - by Bioz Stars, 2026-08
86/100 stars
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90
Hamamatsu scientific cmos orca flash 4 v4
(A) Scanning electron microscopy (SEM) images of the fabricated designs’ main variants (“Rams; “Arrows”; “Tesla”). Low magnification images (top) encompass the entire microfluidic device design, while high magnification images (bottom) detail the respective motif design. (B) <t>Widefield</t> microscopy mosaic image (20× objective) of different neuronal populations (“Source” and “Target”) at 14 days in vitro, selectively expressing mRuby3 (red) and EGFP (cyan), cultured on a microfluidic device with the “Tesla” motif. (C) Schematics of the rationale for each motif design. Green, orange and red arrows indicate axonal outgrowth-permissive, re-routing and blocking capabilities, respectively.
Scientific Cmos Orca Flash 4 V4, 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/eclipse+ti2+e+widefield+fluorescence+microscope/pmc08287531-219-15-18?v=Hamamatsu
Average 90 stars, based on 1 article reviews
scientific cmos orca flash 4 v4 - by Bioz Stars, 2026-08
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90
Hamamatsu orca-fusion digital cmos camera
(A) Scanning electron microscopy (SEM) images of the fabricated designs’ main variants (“Rams; “Arrows”; “Tesla”). Low magnification images (top) encompass the entire microfluidic device design, while high magnification images (bottom) detail the respective motif design. (B) <t>Widefield</t> microscopy mosaic image (20× objective) of different neuronal populations (“Source” and “Target”) at 14 days in vitro, selectively expressing mRuby3 (red) and EGFP (cyan), cultured on a microfluidic device with the “Tesla” motif. (C) Schematics of the rationale for each motif design. Green, orange and red arrows indicate axonal outgrowth-permissive, re-routing and blocking capabilities, respectively.
Orca Fusion Digital Cmos Camera, 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/eclipse+ti2+e+widefield+fluorescence+microscope/pm37963249-234-24-29?v=Hamamatsu
Average 90 stars, based on 1 article reviews
orca-fusion digital cmos camera - by Bioz Stars, 2026-08
90/100 stars
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86
Lumencor Inc orca fusion gen iii camera
(A) Scanning electron microscopy (SEM) images of the fabricated designs’ main variants (“Rams; “Arrows”; “Tesla”). Low magnification images (top) encompass the entire microfluidic device design, while high magnification images (bottom) detail the respective motif design. (B) <t>Widefield</t> microscopy mosaic image (20× objective) of different neuronal populations (“Source” and “Target”) at 14 days in vitro, selectively expressing mRuby3 (red) and EGFP (cyan), cultured on a microfluidic device with the “Tesla” motif. (C) Schematics of the rationale for each motif design. Green, orange and red arrows indicate axonal outgrowth-permissive, re-routing and blocking capabilities, respectively.
Orca Fusion Gen Iii Camera, supplied by Lumencor 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/eclipse+ti2+e+widefield+fluorescence+microscope/pm41549998-243-16-21?v=Lumencor+Inc
Average 86 stars, based on 1 article reviews
orca fusion gen iii camera - by Bioz Stars, 2026-08
86/100 stars
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Image Search Results


(A) Scanning electron microscopy (SEM) images of the fabricated designs’ main variants (“Rams; “Arrows”; “Tesla”). Low magnification images (top) encompass the entire microfluidic device design, while high magnification images (bottom) detail the respective motif design. (B) Widefield microscopy mosaic image (20× objective) of different neuronal populations (“Source” and “Target”) at 14 days in vitro, selectively expressing mRuby3 (red) and EGFP (cyan), cultured on a microfluidic device with the “Tesla” motif. (C) Schematics of the rationale for each motif design. Green, orange and red arrows indicate axonal outgrowth-permissive, re-routing and blocking capabilities, respectively.

Journal: bioRxiv

Article Title: Influence of asymmetric microchannels in the structure and function of engineered neuronal circuits

doi: 10.1101/2024.07.09.602729

Figure Lengend Snippet: (A) Scanning electron microscopy (SEM) images of the fabricated designs’ main variants (“Rams; “Arrows”; “Tesla”). Low magnification images (top) encompass the entire microfluidic device design, while high magnification images (bottom) detail the respective motif design. (B) Widefield microscopy mosaic image (20× objective) of different neuronal populations (“Source” and “Target”) at 14 days in vitro, selectively expressing mRuby3 (red) and EGFP (cyan), cultured on a microfluidic device with the “Tesla” motif. (C) Schematics of the rationale for each motif design. Green, orange and red arrows indicate axonal outgrowth-permissive, re-routing and blocking capabilities, respectively.

Article Snippet: All recordings were obtained using a commercial MEA2100-256 system (Multichannel Systems MCS, Germany) mounted on an incubated (37 °C) inverted widefield microscope (Axiovert 200M, Zeiss or Eclipse Ti2-E, Nikon) stage supplied with humidified 5% CO 2 .

Techniques: Electron Microscopy, Microscopy, In Vitro, Expressing, Cell Culture, Blocking Assay

(A) Widefield microscopy mosaic images (20× objective) of representative neuronal monocultures (seeded on the “Target” compartment) at 14 days in vitro (DIV) for each design. All cultures are expressing EGFP (grayscale). Asterisks mark microchannels that failed to completely block axonal outgrowth before the straight segment of the microchannel (dashed line). B) Percentage of microchannels that completely block axonal outgrowth per design. Filled dots represent the cultures shown on A). C) Normalized average pixel intensity values along the microchannels. The average intensity profiles (and colorized shade for the SD) of 5-6 independent experiments (16 microchannels per experiment) are plotted together with a fitted exponential curve. Per design, a representative microchannel is colorized with the Turbo lookup table (LUT).

Journal: bioRxiv

Article Title: Influence of asymmetric microchannels in the structure and function of engineered neuronal circuits

doi: 10.1101/2024.07.09.602729

Figure Lengend Snippet: (A) Widefield microscopy mosaic images (20× objective) of representative neuronal monocultures (seeded on the “Target” compartment) at 14 days in vitro (DIV) for each design. All cultures are expressing EGFP (grayscale). Asterisks mark microchannels that failed to completely block axonal outgrowth before the straight segment of the microchannel (dashed line). B) Percentage of microchannels that completely block axonal outgrowth per design. Filled dots represent the cultures shown on A). C) Normalized average pixel intensity values along the microchannels. The average intensity profiles (and colorized shade for the SD) of 5-6 independent experiments (16 microchannels per experiment) are plotted together with a fitted exponential curve. Per design, a representative microchannel is colorized with the Turbo lookup table (LUT).

Article Snippet: All recordings were obtained using a commercial MEA2100-256 system (Multichannel Systems MCS, Germany) mounted on an incubated (37 °C) inverted widefield microscope (Axiovert 200M, Zeiss or Eclipse Ti2-E, Nikon) stage supplied with humidified 5% CO 2 .

Techniques: Microscopy, In Vitro, Expressing, Blocking Assay