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fusion scmos camera  (Hamamatsu)

 
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    Structured Review

    Hamamatsu fusion scmos camera
    Fusion 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/fusion+scmos+camera/fusion+bt+scmos+camera/bio_rxiv__2025__07__12__664541-141-23-23
    Average 90 stars, based on 1 article reviews
    fusion scmos camera - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    other:

    Article Title: Dynamics of interaction and internalisation of the antifungal protein PeAfpA into Penicillium digitatum morphotypes.
    Article Snippet: Images and videos of bursting hyphae were captured on a Hamamatsu Fusion sCmos camera with a 40x/0.95NA X-line UPlanXApo Olympus lens mounted on Jo ur na l P re -p ro of

    Article Title: ATR protects centromere identity by promoting DAXX association with PML nuclear bodies.
    Article Snippet: All images were acquired on a Nikon ECLIPSE Ti2 widefield epi-fluorescencemicroscope with a Hamamatsu Fusion sCMOS camera.

    Expressing:

    Article Title: Live-cell imaging of pathogenic fungal hyphae reveal dynamic cellular responses to clinical antifungals
    Article Snippet: .. Additional widefield acquisitions were performed on a temperature regulated Zeiss AxioObserver Z1 equipped with a Hamamatsu Fusion sCMOS camera and a 20x/0.8NA Plan-apo lens with a GFP filter set (Zeiss #62) which captured both GFP and YFP expressing fungi. ..

    Confocal Microscopy:

    Article Title: METTL3 promotes cell cycle progression via activation of transcriptional elongation
    Article Snippet: .. Images for chromosome missegregation defects and chromosome analysis are collected on a Nikon ECLIPSE Ti W2 spinning disk for confocal microscopy with a Hamamatsu Fusion sCMOS camera. .. Image were analyzed using both Nikon’s NIS-elements and Image J (Fiji) software.

    Microscopy:

    Article Title: Chk2 sustains PLK1 activity in mitosis to ensure proper chromosome segregation
    Article Snippet: Cells were washed again with PBS and mounted onto glass slides using ProLong Gold Antifade Mountant (Invitrogen) and left to dry overnight. .. All images were acquired on a Nikon ECLIPSE Ti2 W2 spinning disk confocal microscope with a Hamamatsu Fusion sCMOS camera. .. Image acquisition was managed using NIS-Elements (Nikon).

    Article Title: ATR protects centromere identity by promoting DAXX association with PML nuclear bodies
    Article Snippet: Cells were washed again with PBS for 5 min and mounted onto glass slides using ProLongTM Gold Antifade Mountant (Invitrogen) and left to dry overnight. .. All images were acquired on a Nikon ECLIPSE Ti2 widefield epi-fluorescence microscope with a Hamamatsu Fusion sCMOS camera. .. Image acquisition was managed using NIS-Elements (Nikon).

    Article Title: Chk2 sustains PLK1 activity in mitosis to ensure proper chromosome segregation
    Article Snippet: Cells were washed again with PBS and mounted onto glass slides using ProLong Gold Antifade Mountant (Invitrogen) and left to dry overnight. .. All images were acquired on a Nikon ECLIPSE Ti2 W2 spinning disk confocal microscope with a Hamamatsu Fusion sCMOS camera. .. Image acquisition was managed using NIS-Elements (Nikon).



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    ( a ) Schematic of the ExA-SPIM system. Light enters the system from the laser combiner and is reflected by mirror M1. A cylindrical lens focuses the light in one dimension onto the surface of a tunable lens, which is magnified onto the back focal plane of the excitation through a 1.5×relay consisting of lenses L1 and L2 and mirrors M2 and M3. The excitation objective is oriented vertically and dipped into a liquid immersion chamber. The tunable lens is conjugated to the back focal plane of the excitation objective to enable axial sweeping. A pair of galvo mirrors is used in tandem to translate the position of the light sheet in z (along the optical axis of the detection objective). The detection objective is oriented horizontally. A beam splitter is removed from the lens and replaced with approximately 35 mm of water. A large-format CMOS camera captures images from the detection lens, at a back focusing distance of 50 cm. ( b ) The field of view of the system is 10.6×8.0 mm (13.3 mm diagonal), which is digitized by the camera into a 151-megapixel (MP) image with 0.75 µm/px sampling. Although the optical resolution of the detection lens is ~1.0 µm, the sampling limited resolution based on the Nyquist criterion is ~1.5 µm. The large field of view dramatically reduces the need for tiling. For example, a 3× expanded mouse brain can be captured in only 15 tiles. Representative images of a three expanded mouse brain are shown with a 1 cm scale bar. ( c ) The PSF for 561 nm excitation is shown in the xy , xz , and yz planes. The mean and standard deviation of the lateral and axial full-width half-maximum are shown as a function of x and y position across the full field of view. ( d ) The field curvature and distortion of the system as a function of field position is shown for different wavebands. The field curvature is <2.5× the depth of field (DoF) for all wavebands. This performance is better than ‘Plan’ specified life sciences objectives . ( e ) The relative signal-to-noise ratio (rSNR) of the VP-151MXCMOS camera and an Orca Flash V3 <t>sCMOS</t> <t>camera</t> as a function of imaging speed. The VP-151MX camera provides equivalent SNR at nearly twice the imaging speed.
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    ( a ) Schematic of the ExA-SPIM system. Light enters the system from the laser combiner and is reflected by mirror M1. A cylindrical lens focuses the light in one dimension onto the surface of a tunable lens, which is magnified onto the back focal plane of the excitation through a 1.5×relay consisting of lenses L1 and L2 and mirrors M2 and M3. The excitation objective is oriented vertically and dipped into a liquid immersion chamber. The tunable lens is conjugated to the back focal plane of the excitation objective to enable axial sweeping. A pair of galvo mirrors is used in tandem to translate the position of the light sheet in z (along the optical axis of the detection objective). The detection objective is oriented horizontally. A beam splitter is removed from the lens and replaced with approximately 35 mm of water. A large-format CMOS camera captures images from the detection lens, at a back focusing distance of 50 cm. ( b ) The field of view of the system is 10.6×8.0 mm (13.3 mm diagonal), which is digitized by the camera into a 151-megapixel (MP) image with 0.75 µm/px sampling. Although the optical resolution of the detection lens is ~1.0 µm, the sampling limited resolution based on the Nyquist criterion is ~1.5 µm. The large field of view dramatically reduces the need for tiling. For example, a 3× expanded mouse brain can be captured in only 15 tiles. Representative images of a three expanded mouse brain are shown with a 1 cm scale bar. ( c ) The PSF for 561 nm excitation is shown in the xy , xz , and yz planes. The mean and standard deviation of the lateral and axial full-width half-maximum are shown as a function of x and y position across the full field of view. ( d ) The field curvature and distortion of the system as a function of field position is shown for different wavebands. The field curvature is <2.5× the depth of field (DoF) for all wavebands. This performance is better than ‘Plan’ specified life sciences objectives . ( e ) The relative signal-to-noise ratio (rSNR) of the VP-151MXCMOS camera and an Orca Flash V3 <t>sCMOS</t> <t>camera</t> as a function of imaging speed. The VP-151MX camera provides equivalent SNR at nearly twice the imaging speed.
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    Image Search Results


    ( a ) Schematic of the ExA-SPIM system. Light enters the system from the laser combiner and is reflected by mirror M1. A cylindrical lens focuses the light in one dimension onto the surface of a tunable lens, which is magnified onto the back focal plane of the excitation through a 1.5×relay consisting of lenses L1 and L2 and mirrors M2 and M3. The excitation objective is oriented vertically and dipped into a liquid immersion chamber. The tunable lens is conjugated to the back focal plane of the excitation objective to enable axial sweeping. A pair of galvo mirrors is used in tandem to translate the position of the light sheet in z (along the optical axis of the detection objective). The detection objective is oriented horizontally. A beam splitter is removed from the lens and replaced with approximately 35 mm of water. A large-format CMOS camera captures images from the detection lens, at a back focusing distance of 50 cm. ( b ) The field of view of the system is 10.6×8.0 mm (13.3 mm diagonal), which is digitized by the camera into a 151-megapixel (MP) image with 0.75 µm/px sampling. Although the optical resolution of the detection lens is ~1.0 µm, the sampling limited resolution based on the Nyquist criterion is ~1.5 µm. The large field of view dramatically reduces the need for tiling. For example, a 3× expanded mouse brain can be captured in only 15 tiles. Representative images of a three expanded mouse brain are shown with a 1 cm scale bar. ( c ) The PSF for 561 nm excitation is shown in the xy , xz , and yz planes. The mean and standard deviation of the lateral and axial full-width half-maximum are shown as a function of x and y position across the full field of view. ( d ) The field curvature and distortion of the system as a function of field position is shown for different wavebands. The field curvature is <2.5× the depth of field (DoF) for all wavebands. This performance is better than ‘Plan’ specified life sciences objectives . ( e ) The relative signal-to-noise ratio (rSNR) of the VP-151MXCMOS camera and an Orca Flash V3 sCMOS camera as a function of imaging speed. The VP-151MX camera provides equivalent SNR at nearly twice the imaging speed.

    Journal: eLife

    Article Title: Expansion-assisted selective plane illumination microscopy for nanoscale imaging of centimeter-scale tissues

    doi: 10.7554/eLife.91979

    Figure Lengend Snippet: ( a ) Schematic of the ExA-SPIM system. Light enters the system from the laser combiner and is reflected by mirror M1. A cylindrical lens focuses the light in one dimension onto the surface of a tunable lens, which is magnified onto the back focal plane of the excitation through a 1.5×relay consisting of lenses L1 and L2 and mirrors M2 and M3. The excitation objective is oriented vertically and dipped into a liquid immersion chamber. The tunable lens is conjugated to the back focal plane of the excitation objective to enable axial sweeping. A pair of galvo mirrors is used in tandem to translate the position of the light sheet in z (along the optical axis of the detection objective). The detection objective is oriented horizontally. A beam splitter is removed from the lens and replaced with approximately 35 mm of water. A large-format CMOS camera captures images from the detection lens, at a back focusing distance of 50 cm. ( b ) The field of view of the system is 10.6×8.0 mm (13.3 mm diagonal), which is digitized by the camera into a 151-megapixel (MP) image with 0.75 µm/px sampling. Although the optical resolution of the detection lens is ~1.0 µm, the sampling limited resolution based on the Nyquist criterion is ~1.5 µm. The large field of view dramatically reduces the need for tiling. For example, a 3× expanded mouse brain can be captured in only 15 tiles. Representative images of a three expanded mouse brain are shown with a 1 cm scale bar. ( c ) The PSF for 561 nm excitation is shown in the xy , xz , and yz planes. The mean and standard deviation of the lateral and axial full-width half-maximum are shown as a function of x and y position across the full field of view. ( d ) The field curvature and distortion of the system as a function of field position is shown for different wavebands. The field curvature is <2.5× the depth of field (DoF) for all wavebands. This performance is better than ‘Plan’ specified life sciences objectives . ( e ) The relative signal-to-noise ratio (rSNR) of the VP-151MXCMOS camera and an Orca Flash V3 sCMOS camera as a function of imaging speed. The VP-151MX camera provides equivalent SNR at nearly twice the imaging speed.

    Article Snippet: A comparison of the selected lens and camera sensor with a state-of-the-art cleared tissue objective lens (Nikon 20×GLYC) and sCMOS camera (Hamamatsu Orca BT-Fusion) is shown in ( ).

    Techniques: Sampling, Standard Deviation, Imaging

    ( a ) Nikon 20× GLYC next to the VEO_JM DIAMOND 5.0× / F1.3 lens. ( b ) Traditional sCMOS camera with 2048×2048 pixels next to the VP-151MX camera with the Sony IMX411 sensor with 14192×10,640 pixels.

    Journal: eLife

    Article Title: Expansion-assisted selective plane illumination microscopy for nanoscale imaging of centimeter-scale tissues

    doi: 10.7554/eLife.91979

    Figure Lengend Snippet: ( a ) Nikon 20× GLYC next to the VEO_JM DIAMOND 5.0× / F1.3 lens. ( b ) Traditional sCMOS camera with 2048×2048 pixels next to the VP-151MX camera with the Sony IMX411 sensor with 14192×10,640 pixels.

    Article Snippet: A comparison of the selected lens and camera sensor with a state-of-the-art cleared tissue objective lens (Nikon 20×GLYC) and sCMOS camera (Hamamatsu Orca BT-Fusion) is shown in ( ).

    Techniques: