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eclipse ti 2 yokogawa csu w1 sora spinning disk microscope  (Yokogawa Electric)


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    Structured Review

    Yokogawa Electric eclipse ti 2 yokogawa csu w1 sora spinning disk microscope
    Eclipse Ti 2 Yokogawa Csu W1 Sora Spinning Disk Microscope, supplied by Yokogawa Electric, used in various techniques. Bioz Stars score: 99/100, based on 557 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+ti+2+microscope/CSU-W1+SoRa/pmc13087726-445-7-9
    Average 99 stars, based on 557 article reviews
    eclipse ti 2 yokogawa csu w1 sora spinning disk microscope - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Microscopy:

    Article Title: Ribosome biogenesis bottlenecks reveal vulnerabilities in cancer
    Article Snippet: .. Images were acquired on a Nikon CSU-W1 SoRa spinning-disk confocal microscope (Yokogawa) capable of pixel-reassignment super-resolution imaging. ..

    Article Title: PROTAC internalization and target degradation require clathrin-mediated endocytosis
    Article Snippet: Olympus spinning disk confocal microscopy system was used for dynamic observation of live cell plasma membranes. .. This system integrates a Yokogawa CSU-W1 SoRa scanning unit and is built upon the Olympus IX83 microscope platform, equipped with a 100× Plan-Apochromat oil immersion objective (NA 1.5). .. Fluorescence signals were captured using a Hamamatsu ORCA C13440-20CU CMOS camera.

    Article Title: The SMARCA4 subunit of the SWI/SNF complex prevents genome instability at G quadruplexes.
    Article Snippet: Cells were treated with 20 μM PDS for 3 or 6 h. Cells were fixed with 4% paraformaldehyde for 15 minutes, permeabilised with 0.5% Triton X-100 for 8 min, and blocked with 1% BSA for 30 min. Coverslips were incubated in γH2A.X rabbit polyclonal antibody (Cell Signalling Technology, #2577, 1:1000) at 4°C overnight, and in Alexa Fluor 488-conjugated Donkey anti-Rabbit secondary antibody (Invitrogen, A-21206, 1:1000) at room temperature for 1 h. Slides were mounted with VECTASHIELD Antifade mounting media with DAPI. .. Imaging was performed using a CSU-W1 Yokogawa Advanced Spinning Disk (PARylation) or CSU-W1 SoRa Yokogawa Super-Resolution Spinning Disk Confocal microscope (RPA2), or Zeiss Axio Observer Z1 Marianas Microscope (yH2AX) equipped with SlideBook software (3i). ..

    Article Title: Arp2/3 involvement in intercellular bridge membrane fluctuations and constriction during neural stem cell divisions
    Article Snippet: .. Brain explants were imaged using a Nikon Eclipse Ti-2 Yokogawa CSU-W1 SoRa spinning disk microscope equipped with dual Photometrics Prime BSI sCMOS cameras using a 60x H 2 O objective with a numerical aperture of 1.2 (for all data except C and the final clip in ). .. For C and the final clip in , brain explants were imaged using an Olympus IX-83 Yokogawa CSU-W1 SoRa spinning disk microscope equipped with dual Hamamatsu ORCA-Fusion BT sCMOS cameras using a 60x Silicone objective with a numerical aperture of 1.3.

    Article Title: Intrinsically disordered ligands for the control of receptor uptake by endocytosis
    Article Snippet: .. Live cell images were collected on an Olympus spinning disk confocal microscope, which featured a Yokogawa CSU-W1 SoRa confocal scanner unit and an Olympus IX83 microscope equipped with a 100xPlan-Aporchromat 1.5 NA oil-immersion objective. .. Fluorescence emission was captured using a Hamamatsu ORCA C13440-20CU CMOS camera.

    Article Title: Arp2/3 involvement in intercellular bridge membrane fluctuations and constriction during neural stem cell divisions
    Article Snippet: Brain explants were imaged using a Nikon Eclipse Ti-2 Yokogawa CSU-W1 SoRa spinning disk microscope equipped with dual Photometrics Prime BSI sCMOS cameras using a 60x H 2 O objective with a numerical aperture of 1.2 (for all data except C and the final clip in ). .. For C and the final clip in , brain explants were imaged using an Olympus IX-83 Yokogawa CSU-W1 SoRa spinning disk microscope equipped with dual Hamamatsu ORCA-Fusion BT sCMOS cameras using a 60x Silicone objective with a numerical aperture of 1.3. ..

    Article Title: Influence of stabilizer, size and physical state of lipid nanoparticles on uptake by THP-1 macrophages.
    Article Snippet: .. The slides were stored in the refrigerator until examination with an inverted Eclipse Ti2-E microscope (Nikon, Düsseldorf, Germany) equipped with a CFI Plan Apochromat Lambda D 60X objective (1.40 oil, Nikon, Düsseldorf, Germany), a CSU W1 SORA spinning disk unit (Yokogawa, Tokyo, Japan) and sCMOS cameras (Prime BSI, Teledyne Photometrics, Tucson, AZ, USA). .. The instrument was controlled by Visiview Premier software (Visitron Systems, Munich, Germany).

    Imaging:

    Article Title: Ribosome biogenesis bottlenecks reveal vulnerabilities in cancer
    Article Snippet: .. Images were acquired on a Nikon CSU-W1 SoRa spinning-disk confocal microscope (Yokogawa) capable of pixel-reassignment super-resolution imaging. ..

    Article Title: The SMARCA4 subunit of the SWI/SNF complex prevents genome instability at G quadruplexes.
    Article Snippet: Cells were treated with 20 μM PDS for 3 or 6 h. Cells were fixed with 4% paraformaldehyde for 15 minutes, permeabilised with 0.5% Triton X-100 for 8 min, and blocked with 1% BSA for 30 min. Coverslips were incubated in γH2A.X rabbit polyclonal antibody (Cell Signalling Technology, #2577, 1:1000) at 4°C overnight, and in Alexa Fluor 488-conjugated Donkey anti-Rabbit secondary antibody (Invitrogen, A-21206, 1:1000) at room temperature for 1 h. Slides were mounted with VECTASHIELD Antifade mounting media with DAPI. .. Imaging was performed using a CSU-W1 Yokogawa Advanced Spinning Disk (PARylation) or CSU-W1 SoRa Yokogawa Super-Resolution Spinning Disk Confocal microscope (RPA2), or Zeiss Axio Observer Z1 Marianas Microscope (yH2AX) equipped with SlideBook software (3i). ..

    Software:

    Article Title: The SMARCA4 subunit of the SWI/SNF complex prevents genome instability at G quadruplexes.
    Article Snippet: Cells were treated with 20 μM PDS for 3 or 6 h. Cells were fixed with 4% paraformaldehyde for 15 minutes, permeabilised with 0.5% Triton X-100 for 8 min, and blocked with 1% BSA for 30 min. Coverslips were incubated in γH2A.X rabbit polyclonal antibody (Cell Signalling Technology, #2577, 1:1000) at 4°C overnight, and in Alexa Fluor 488-conjugated Donkey anti-Rabbit secondary antibody (Invitrogen, A-21206, 1:1000) at room temperature for 1 h. Slides were mounted with VECTASHIELD Antifade mounting media with DAPI. .. Imaging was performed using a CSU-W1 Yokogawa Advanced Spinning Disk (PARylation) or CSU-W1 SoRa Yokogawa Super-Resolution Spinning Disk Confocal microscope (RPA2), or Zeiss Axio Observer Z1 Marianas Microscope (yH2AX) equipped with SlideBook software (3i). ..

    Inverted Microscopy:

    Article Title: ER-associated control of axonal vesicle trafficking during neuronal development
    Article Snippet: .. Cells were imaged with a Yokogawa CSU-W1 SoRa spinning disk confocal, which is built on a Ti2 inverted microscope and contains a Hamamatsu ORCA-FusionBT sCMOS camera (Nikon). ..



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