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2d-array scanning confocal microscope infinity4  (Visitech Inc)

 
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    Visitech Inc 2d-array scanning confocal microscope infinity4
    2d Array Scanning Confocal Microscope Infinity4, supplied by Visitech 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/2d+array/2d+array+scanning+confocal+microscope+infinity4/pm40651941-668-5-10
    Average 90 stars, based on 1 article reviews
    2d-array scanning confocal microscope infinity4 - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    other:

    Article Title: Cholesterol inhibits assembly and oncogenic activation of the EphA2 receptor
    Article Snippet: After curing, cells were imaged using a VT-Hawk 2D array scanning confocal microscope (Visitech intl.) mounted to an IX-83 inverted optical microscope (Olympus).

    Article Title: Calcium Handling Remodeling Underlies Impaired Sympathetic Stress Response in Ventricular Myocardium from Cacna1c Haploinsufficient Rats.
    Article Snippet: Ca2+ transients (CaTs) were recorded using the linescan mode of a confocal microscope (LSM510, Zeiss, Oberkochen, Germany) or at a 2D-array scanning microscope (VT-Hawk, Visitech, Sunderland, UK).

    Article Title: Endogenous oncogenic KRAS expression increases cell proliferation and motility in near-diploid hTERT RPE-1 cells
    Article Snippet: Cell images were acquired using a 2D array scanning laser confocal microscope (Infinity 3, Visitech) using a 60×/1.4 Plan Apo objective lens (Nikon).

    Article Title: Highly adaptable deep-learning platform for automated detection and analysis of vesicle exocytosis.
    Article Snippet: The data was recorded with 2D-array scanning confocal microscope (Infinity4, Visitech, Sunderland, UK) equipped with a NIKON 60x oil immersion objective (NA = 1.40) and a sCMOS Flash4 V2 camera fromHamamatsu (Hamamatsu Photonics Deutschland GmbH, Herrsching am Ammersee, Germany).

    Article Title: Highly adaptable deep-learning platform for automated detection and analysis of vesicle exocytosis
    Article Snippet: The data was recorded with 2D-array scanning confocal microscope (Infinity4, Visitech, Sunderland, UK) equipped with a NIKON 60x oil immersion objective (NA = 1.40) and a sCMOS Flash4 V2 camera from Hamamatsu (Hamamatsu Photonics Deutschland GmbH, Herrsching am Ammersee, Germany).

    Article Title: Cholesterol inhibits assembly and oncogenic activation of the EphA2 receptor.
    Article Snippet: After curing, cells were imaged using a VTHawk 2D array scanning confocalmicroscope (Visitech intl.) mounted to an IX-83 inverted optical microscope (Olympus).

    Microscopy:

    Article Title: Polypeptide conjugates for intracellular delivery of nucleic acids
    Article Snippet: .. Cells were washed twice with DPBS and treated with the CRC5/5′-FAM-siRNA complex for 2 h. After removal of the medium, the cells were gently washed with DPBS twice and imaged on a Nikon A1R live-cell confocal microscope equipped with a 100× oil objective or a Visitech Infinity 3 Hawk 2D-array live cell confocal microscope equipped with 60× oil objective. .. Data were analyzed using NISElemenets AR or MetaMorph Premier.

    Article Title: Endogenous oncogenic KRAS expression increases cell proliferation and motility in near-diploid hTERT RPE-1 cells.
    Article Snippet: Received for publication, September 8, 2023, and in revised form, April 27, 2024 Published, Papers in Press, May 23, 2024, https://doi.org/10.1016/j.jbc.2024.107409 Naushin L. Hindul , Lauren R. Abbott , Sumaya M. D. Adan , Kornelis R. Straatman , Andrew M. Fry, Kouji Hirota, and Kayoko Tanaka* From the Department of Molecular and Cell Biology, University of Leicester, Leicester, UK; Advanced Imaging Facility, University of Leicester, Leicester, UK; Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Hachioji, Japan



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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