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orca er cold ccd camera; detector array 1344 × 1024 px  (Hamamatsu)

 
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    Structured Review

    Hamamatsu orca er cold ccd camera; detector array 1344 × 1024 px
    Breaking the Gigapixel limit of a confluent confocal panorama image : A 2,8 Gigapixel size confocal mosaic, built up from 3000 (50 columns × 60 rows) individual confocal images (A), using the ImageLab/Virtual Microscope software. The internal structures of a mouse head are visualized with eosin fluorescence at 63X/NA1.25, individual images cover an area of 135 μm × 103 μm (B), captured at binning 1 (1344 × <t>1024</t> pixels) and 200 pixels overlap. After image processing in the ImageLab/Virtual Microscope software the final seamless confocal panorama show an area of 5,75 mm × 4,98 mm. The original resolution of each individual image is preserved in the final montage, allowing the user to zoom in on details at single cell level (C).
    Orca Er Cold Ccd Camera; Detector Array 1344 × 1024 Px, 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/array+detector/pmc02515298-54-37-43?v=Hamamatsu
    Average 90 stars, based on 1 article reviews
    orca er cold ccd camera; detector array 1344 × 1024 px - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "Extended Field Laser Confocal Microscopy (EFLCM): Combining automated Gigapixel image capture with in silico virtual microscopy"

    Article Title: Extended Field Laser Confocal Microscopy (EFLCM): Combining automated Gigapixel image capture with in silico virtual microscopy

    Journal: BMC Medical Imaging

    doi: 10.1186/1471-2342-8-13

    Breaking the Gigapixel limit of a confluent confocal panorama image : A 2,8 Gigapixel size confocal mosaic, built up from 3000 (50 columns × 60 rows) individual confocal images (A), using the ImageLab/Virtual Microscope software. The internal structures of a mouse head are visualized with eosin fluorescence at 63X/NA1.25, individual images cover an area of 135 μm × 103 μm (B), captured at binning 1 (1344 × 1024 pixels) and 200 pixels overlap. After image processing in the ImageLab/Virtual Microscope software the final seamless confocal panorama show an area of 5,75 mm × 4,98 mm. The original resolution of each individual image is preserved in the final montage, allowing the user to zoom in on details at single cell level (C).
    Figure Legend Snippet: Breaking the Gigapixel limit of a confluent confocal panorama image : A 2,8 Gigapixel size confocal mosaic, built up from 3000 (50 columns × 60 rows) individual confocal images (A), using the ImageLab/Virtual Microscope software. The internal structures of a mouse head are visualized with eosin fluorescence at 63X/NA1.25, individual images cover an area of 135 μm × 103 μm (B), captured at binning 1 (1344 × 1024 pixels) and 200 pixels overlap. After image processing in the ImageLab/Virtual Microscope software the final seamless confocal panorama show an area of 5,75 mm × 4,98 mm. The original resolution of each individual image is preserved in the final montage, allowing the user to zoom in on details at single cell level (C).

    Techniques Used: Microscopy, Software, Fluorescence

    Example of application of the EFLCM method : To visualize thousands of cells growing in monolayer – for automatic and objective quantitation of epigenetic effects of the transformation associated viral nuclear antigen HHV8 LANA fused to green fluorescence protein in a transient transfection assay. The blue color is Hoecsht 33342 fluorescence showing DNA. The mosaic is built up from 100 images (10 columns × 10 rows) captured at 16X/NA O.5. Individual images covers an area of 522 μm × 398 μm. Images are captured at binning 1 (1344 × 1024 pixels) with 100 pixels overlap resulting in a final area of the seamless panorama, after image processing in the ImageLab/Virtual Microscope, of 4,82 mm × 3,58 mm.
    Figure Legend Snippet: Example of application of the EFLCM method : To visualize thousands of cells growing in monolayer – for automatic and objective quantitation of epigenetic effects of the transformation associated viral nuclear antigen HHV8 LANA fused to green fluorescence protein in a transient transfection assay. The blue color is Hoecsht 33342 fluorescence showing DNA. The mosaic is built up from 100 images (10 columns × 10 rows) captured at 16X/NA O.5. Individual images covers an area of 522 μm × 398 μm. Images are captured at binning 1 (1344 × 1024 pixels) with 100 pixels overlap resulting in a final area of the seamless panorama, after image processing in the ImageLab/Virtual Microscope, of 4,82 mm × 3,58 mm.

    Techniques Used: Quantitation Assay, Transformation Assay, Fluorescence, Transient Transfection Assay, Microscopy



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    Image Search Results


    Signal amplitude from the CROSSmini detector with signal fitting and zoomed in views. Figures A, B and C, on the left, shows the signal amplitude from the CROSSmini detector of a spill duration for energy level 70.2, 150.2, and 228.7 MeV, respectively, with nominal beam current 8 MU/s. The red line represents the original signal from CROSSmini and the black line represents the piecewise fitting for the edges. On the right is the zoomed in view of the fitting. The piecewise fitting quantifies the risetime ( t rise ) and measured nominal beam current ( I 0 , measured ).

    Journal: International Journal of Particle Therapy

    Article Title: Phenomenological Study of Intra-Spill Break Spots in Dose-Driven Continuous Scanning Proton Therapy

    doi: 10.1016/j.ijpt.2026.101315

    Figure Lengend Snippet: Signal amplitude from the CROSSmini detector with signal fitting and zoomed in views. Figures A, B and C, on the left, shows the signal amplitude from the CROSSmini detector of a spill duration for energy level 70.2, 150.2, and 228.7 MeV, respectively, with nominal beam current 8 MU/s. The red line represents the original signal from CROSSmini and the black line represents the piecewise fitting for the edges. On the right is the zoomed in view of the fitting. The piecewise fitting quantifies the risetime ( t rise ) and measured nominal beam current ( I 0 , measured ).

    Article Snippet: The beam current was measured using a CROSSmini 2D strip ionization chamber detector array (Liverage Biomedical Inc, Taiwan) positioned at the isocenter plane.

    Techniques:

    Signal amplitude from the CROSSmini detector with signal fitting. shows the signal amplitude as a function of time measured by the CROSSmini detector and the piecewise fittings. Figures A, B, and C are measurements for energy level 70.2 MeV with nominal beam current 8, 14, and 20 MU/s, respectively. Figures D, E, and F are the measurements for energy level 228.7 MeV with nominal beam current 8, 14, and 20 MU/s, respectively.

    Journal: International Journal of Particle Therapy

    Article Title: Phenomenological Study of Intra-Spill Break Spots in Dose-Driven Continuous Scanning Proton Therapy

    doi: 10.1016/j.ijpt.2026.101315

    Figure Lengend Snippet: Signal amplitude from the CROSSmini detector with signal fitting. shows the signal amplitude as a function of time measured by the CROSSmini detector and the piecewise fittings. Figures A, B, and C are measurements for energy level 70.2 MeV with nominal beam current 8, 14, and 20 MU/s, respectively. Figures D, E, and F are the measurements for energy level 228.7 MeV with nominal beam current 8, 14, and 20 MU/s, respectively.

    Article Snippet: The beam current was measured using a CROSSmini 2D strip ionization chamber detector array (Liverage Biomedical Inc, Taiwan) positioned at the isocenter plane.

    Techniques:

    t rise comparison between analytical and measured. The blue and red plots represent the analytically derived t rise and CROSSmini measured t rise , respectively, across the various nominal beam current settings.

    Journal: International Journal of Particle Therapy

    Article Title: Phenomenological Study of Intra-Spill Break Spots in Dose-Driven Continuous Scanning Proton Therapy

    doi: 10.1016/j.ijpt.2026.101315

    Figure Lengend Snippet: t rise comparison between analytical and measured. The blue and red plots represent the analytically derived t rise and CROSSmini measured t rise , respectively, across the various nominal beam current settings.

    Article Snippet: The beam current was measured using a CROSSmini 2D strip ionization chamber detector array (Liverage Biomedical Inc, Taiwan) positioned at the isocenter plane.

    Techniques: Comparison, Derivative Assay