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confocal microscope zeiss lsm780 elyra s.1 system  (Carl Zeiss)


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    Carl Zeiss confocal microscope zeiss lsm780 elyra s.1 system
    Confocal Microscope Zeiss Lsm780 Elyra S.1 System, supplied by Carl Zeiss, 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/elyra-s%2E1/2+apotome/pm40241097-39-15-17
    Average 90 stars, based on 1 article reviews
    confocal microscope zeiss lsm780 elyra s.1 system - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Staining:

    Article Title: The polarity protein Par3 coordinates positively self-renewal and negatively invasiveness in glioblastoma
    Article Snippet: Stained cells, mounted in ProLong Glass Antifade Mountant (Thermo Fischer Scientific) were analyzed in a structured illumination microscopy (SIM) super-resolution microscope Zeiss ELYRA-S.1 (Carl Zeiss AB, Stockholm, Sweden).

    Article Title: The polarity protein Par3 coordinates positively self-renewal and negatively invasiveness in glioblastoma.
    Article Snippet: Stained cells, mounted in ProLong Glass Antifade Mountant (Thermo Fischer Scientific) were analyzed in a structured illumination microscopy (SIM) superresolution microscope Zeiss ELYRA-S.1 (Carl Zeiss AB, Stockholm, Sweden).

    Microscopy:

    Article Title: The polarity protein Par3 coordinates positively self-renewal and negatively invasiveness in glioblastoma
    Article Snippet: Stained cells, mounted in ProLong Glass Antifade Mountant (Thermo Fischer Scientific) were analyzed in a structured illumination microscopy (SIM) super-resolution microscope Zeiss ELYRA-S.1 (Carl Zeiss AB, Stockholm, Sweden).

    Article Title: The polarity protein Par3 coordinates positively self-renewal and negatively invasiveness in glioblastoma.
    Article Snippet: Stained cells, mounted in ProLong Glass Antifade Mountant (Thermo Fischer Scientific) were analyzed in a structured illumination microscopy (SIM) superresolution microscope Zeiss ELYRA-S.1 (Carl Zeiss AB, Stockholm, Sweden).



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    Representative 3D projections of <t>structured</t> <t>illumination</t> super-resolution <t>microscopy</t> of PEG-tether-supported proteolipobeads. Panels (A)–(D) were obtained from summed Z-projections of the SIMs Z stacks. (A, A′) Linear2k-PEG-amine conjugated with 4-FB. (B, B′) Linear20k-PEG-amine conjugated with 4-FB. (C, C′) 4arm20k-PEG-amine conjugated with 4-FB. (D, D′) 8arm20k-PEG-amine conjugated with 4-FB. The right panels (A′)–(D′) indicate the equatorial sections only. The white asterisks indicate representative visible inhomogeneities. The lipid reporter DiO (green) distribution is shown. Scale bar: 5 μm.
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    Representative 3D projections of <t>structured</t> <t>illumination</t> super-resolution <t>microscopy</t> of PEG-tether-supported proteolipobeads. Panels (A)–(D) were obtained from summed Z-projections of the SIMs Z stacks. (A, A′) Linear2k-PEG-amine conjugated with 4-FB. (B, B′) Linear20k-PEG-amine conjugated with 4-FB. (C, C′) 4arm20k-PEG-amine conjugated with 4-FB. (D, D′) 8arm20k-PEG-amine conjugated with 4-FB. The right panels (A′)–(D′) indicate the equatorial sections only. The white asterisks indicate representative visible inhomogeneities. The lipid reporter DiO (green) distribution is shown. Scale bar: 5 μm.
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    Image Search Results


    Representative 3D projections of structured illumination super-resolution microscopy of PEG-tether-supported proteolipobeads. Panels (A)–(D) were obtained from summed Z-projections of the SIMs Z stacks. (A, A′) Linear2k-PEG-amine conjugated with 4-FB. (B, B′) Linear20k-PEG-amine conjugated with 4-FB. (C, C′) 4arm20k-PEG-amine conjugated with 4-FB. (D, D′) 8arm20k-PEG-amine conjugated with 4-FB. The right panels (A′)–(D′) indicate the equatorial sections only. The white asterisks indicate representative visible inhomogeneities. The lipid reporter DiO (green) distribution is shown. Scale bar: 5 μm.

    Journal: Langmuir

    Article Title: Supported Biomembrane Systems Incorporating Multiarm Polymers and Bioorthogonal Tethering

    doi: 10.1021/acs.langmuir.4c00176

    Figure Lengend Snippet: Representative 3D projections of structured illumination super-resolution microscopy of PEG-tether-supported proteolipobeads. Panels (A)–(D) were obtained from summed Z-projections of the SIMs Z stacks. (A, A′) Linear2k-PEG-amine conjugated with 4-FB. (B, B′) Linear20k-PEG-amine conjugated with 4-FB. (C, C′) 4arm20k-PEG-amine conjugated with 4-FB. (D, D′) 8arm20k-PEG-amine conjugated with 4-FB. The right panels (A′)–(D′) indicate the equatorial sections only. The white asterisks indicate representative visible inhomogeneities. The lipid reporter DiO (green) distribution is shown. Scale bar: 5 μm.

    Article Snippet: The structured illumination microscopy was performed using a Zeiss ELYRA S.1 system in the DiO green channel (laser excitation 488 nm, HR Diode 488–100 mW, 2%; gain = 20, exposure = 100 ms, BP filter detection, 495–550 nm).

    Techniques: Super-Resolution Microscopy