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Hamamatsu flash 4.0 scmos camera
Flash 4.0 Scmos 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/scmos+camera+flash+4%2E0/flash+4+0+scmos+camera/pmc12172305-671-6-5
Average 90 stars, based on 1 article reviews
flash 4.0 scmos camera - by Bioz Stars, 2026-11
90/100 stars

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Related Articles

other:

Article Title: TorsinA is essential for neuronal nuclear pore complex localization and maturation.
Article Snippet: As lifelong interphase cells, neurons face an array of unique challenges.. A key challenge is regulating nuclear pore complex (NPC) biogenesis and localization, the mechanisms of which are largely unknown.. Here we identify neuronal maturation as a period of strongly upregulated NPC biogenesis.

Article Title: Dynamic high-speed high-sensitivity imaging device and imaging method
Article Snippet: An sCMOS camera Flash 4.0 manufactured by Hamamatsu Photonics K.K. was used as a sensor.

Imaging:

Article Title: Light‐Based Juxtacrine Signaling Between Synthetic Cells
Article Snippet: GUVs were made by encapsulating 20 μL inner solution containing 50 mM Tris-HCl (pH 7.4), 300 mM glucose, 450 nM iLID-6xHis, 100 nM SspB-mCherry, and 10% v/v OptiPrep (SigmaAldrich). .. After collection, 50 μL of GUV solution was transferred to a 96-well clear flat bottom plate and kept in the dark for 30 min before illumination and epifluorescence imaging using a Nikon TiE inverted microscope equipped with an oil immersion Plane Apochromat 60× objective (NA 1.40), a sCMOS camera (Flash 4.0; Hamamatsu Photonics, Japan), and an HBO 100 W/2 mercury bulb. ..

Article Title: TorsinA is essential for the timing and localization of neuronal nuclear pore complex biogenesis
Article Snippet: Gels were covered with clean ddH2O and imaged on ECLIPSE Ti inverted laser-scanning Nikon A1 confocal microscope with a 60x Apochromat water immersion (NA 1.2) objective using NIS-Elements AR (Nikon). .. SIM imaging was conducted on a Nikon N-SIM microscope equipped with an sCMOS camera (Flash 4.0; Hamamatsu Photonics, Japan) and LU-NV laser unit (Nikon) using a 100x Apochromat oil objective (NA 1.49). ..

Inverted Microscopy:

Article Title: Light‐Based Juxtacrine Signaling Between Synthetic Cells
Article Snippet: GUVs were made by encapsulating 20 μL inner solution containing 50 mM Tris-HCl (pH 7.4), 300 mM glucose, 450 nM iLID-6xHis, 100 nM SspB-mCherry, and 10% v/v OptiPrep (SigmaAldrich). .. After collection, 50 μL of GUV solution was transferred to a 96-well clear flat bottom plate and kept in the dark for 30 min before illumination and epifluorescence imaging using a Nikon TiE inverted microscope equipped with an oil immersion Plane Apochromat 60× objective (NA 1.40), a sCMOS camera (Flash 4.0; Hamamatsu Photonics, Japan), and an HBO 100 W/2 mercury bulb. ..

Fluorescence:

Article Title: Analysis device
Article Snippet: .. A fluorescence-labeled single cell solution as described above was spread on a glass slide and a large number of fluorescence images of a single-cell group were captured by an sCMOS camera (Flash 4.0 manufactured by Hamamatsu Photonics K. K.) using a fluorescence microscope. ..

Article Title: Analysis device
Article Snippet: .. A fluorescence-labeled single cell solution as described above was spread on a glass slide and a large number of fluorescence images of a single-cell group were captured by an sCMOS camera (Flash 4.0 manufactured by Hamamatsu Photonics K.K.) using a fluorescence microscope. ..

Single Cell:

Article Title: Analysis device
Article Snippet: .. A fluorescence-labeled single cell solution as described above was spread on a glass slide and a large number of fluorescence images of a single-cell group were captured by an sCMOS camera (Flash 4.0 manufactured by Hamamatsu Photonics K. K.) using a fluorescence microscope. ..

Article Title: Analysis device
Article Snippet: .. A fluorescence-labeled single cell solution as described above was spread on a glass slide and a large number of fluorescence images of a single-cell group were captured by an sCMOS camera (Flash 4.0 manufactured by Hamamatsu Photonics K.K.) using a fluorescence microscope. ..

Microscopy:

Article Title: Analysis device
Article Snippet: .. A fluorescence-labeled single cell solution as described above was spread on a glass slide and a large number of fluorescence images of a single-cell group were captured by an sCMOS camera (Flash 4.0 manufactured by Hamamatsu Photonics K. K.) using a fluorescence microscope. ..

Article Title: Analysis device
Article Snippet: .. A fluorescence-labeled single cell solution as described above was spread on a glass slide and a large number of fluorescence images of a single-cell group were captured by an sCMOS camera (Flash 4.0 manufactured by Hamamatsu Photonics K.K.) using a fluorescence microscope. ..

Article Title: TorsinA is essential for the timing and localization of neuronal nuclear pore complex biogenesis
Article Snippet: Gels were covered with clean ddH2O and imaged on ECLIPSE Ti inverted laser-scanning Nikon A1 confocal microscope with a 60x Apochromat water immersion (NA 1.2) objective using NIS-Elements AR (Nikon). .. SIM imaging was conducted on a Nikon N-SIM microscope equipped with an sCMOS camera (Flash 4.0; Hamamatsu Photonics, Japan) and LU-NV laser unit (Nikon) using a 100x Apochromat oil objective (NA 1.49). ..

Article Title: Engineering paralog-specific PSD-95 recombinant binders as minimally interfering multimodal probes for advanced imaging techniques
Article Snippet: .. 912 Images were acquired on an inverted Leica DMi8 microscope (Leica Microsystems, Wetzlar, Germany) equipped with a Flash 4.0 913 sCMOS camera (Hamamatsu, Hamamatsu, Japan). .. The illumination system used was a Cool LED PE-4000 (CoolLED, Andover, USA).



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