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lsm 780 inverted confocal microscope  (Carl Zeiss)


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    Carl Zeiss lsm 780 inverted confocal microscope
    Lsm 780 Inverted Confocal Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 2152 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lsm+780+confocal+microscope/Primovert+Compact+Inverted+Microscope/pm41810243-56-6-5
    Average 99 stars, based on 2152 article reviews
    lsm 780 inverted confocal microscope - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    other:

    Article Title:
    Article Snippet: 139 Sample brains were imaged under a Zeiss LSM 780 or 880 confocal microscope with a 140 40× C-Apochromat water-immersion objective lens (N.A. value 1.2, working distance 220 141 μm).

    Article Title: The STING pathway drives noninflammatory neurodegeneration in NGLY1 deficiency
    Article Snippet: Fluorophore-conjugated secondary antibodies were used as follows: Goat anti-Rabbit IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor Plus 488 (cat #A32731, 1:200 dilution; Thermo Fisher Scientific); Donkey anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor 546 (cat #A10036, 1:200 dilution; Thermo Fisher Scientific); Donkey anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor 647 (cat #A-31571, 1:500 dilution; Thermo Fisher Scientific).

    Article Title:
    Article Snippet: High magnification fluorescent images were acquired using a Zeiss LSM 780 or LSM 880 confocal microscope.

    Microscopy:

    Article Title: Supporting Information for Redefining the human corneal immune compartment using dynamic intravital imaging
    Article Snippet: .. After drying, tile scans of the corneal basal epithelium were acquired using a Zeiss LSM 780 confocal microscope. ..

    Article Title: Integrative spatial omics reveals distinct tumor-promoting multicellular niches and immunosuppressive mechanisms in Black American and White American patients with TNBC
    Article Snippet: .. Finally, images were acquired using a Zeiss LSM 780 confocal microscope, and the fluorescent images were processed using Zen software (Zeiss). ..

    Article Title: The SV40 T-ag nuclear localization signal affects Toxoplasma gondii viability by targeting importin α
    Article Snippet: Samples were blocked with 3% Bovine Serum Albumin (BSA) in 1X PBS for one hour, then incubated with rabbit anti-HA primary antibody (1:500 dilution, CST) for two hours, followed by a goat anti-rabbit secondary antibody conjugated to Alexa 568 (1:400 dilution, Invitrogen) for one hour. .. Images were acquired by a Zeiss LSM 780 Confocal microscope with 100X objective or a Zeiss Observer Z1 Spinning Disc microscope with 40X or 63X objectives. .. To quantify GFP-positive parasitophorous vacuoles, 15 fields were imaged from each replicate in the Zeiss Observer Z1 Spinning Disc microscope at 40X.

    Article Title: Stem and progenitor cell proliferation are independently regulated by cell type-specific cyclinD genes.
    Article Snippet: .. Images were taken on either a Zeiss LSM 780 confocal microscope or Nikon Ti2 Eclipse equipped with a CSU-W1 Yokogawa spinning disk. .. Guides were diluted to 100 μM in Nuclease-free duplex buffer (IDT).

    Article Title: L-type calcium channel blockers at therapeutic concentrations are not linked to CRAC channels and heart failure.
    Article Snippet: .. On the day of the experiment, the coverslips were mounted in a Teflon chamber, the cells bathed in HBSS that was nominally Ca2+-free (no added CaCl2), and the chamber mounted on the stage of a Zeiss LSM 780 confocal microscope equipped with a 20× objective (N.A. ..

    Software:

    Article Title: Integrative spatial omics reveals distinct tumor-promoting multicellular niches and immunosuppressive mechanisms in Black American and White American patients with TNBC
    Article Snippet: .. Finally, images were acquired using a Zeiss LSM 780 confocal microscope, and the fluorescent images were processed using Zen software (Zeiss). ..



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    ( A ) Stereoscopic microscopy of the MTU at different time points of the tissue development process. ( B ) Culture conditions for muscle tissue maturation, accounting for culture in growth medium for 4 days and myogenic differentiation medium for 11 days after mounting on the tissue maturation template under mechanical tension. H&E staining ( C ) and confocal imaging ( D ) of the muscle tissue, tendon-muscle interface, and tendon structure on day 15. In (C), red arrowheads indicate myotubes. In (D), the yellow dashed line represents the interface border between the two tissues, as determined by manual positioning of the <t>microscope.</t> Orange and red asterisks indicate the muscle and tendon sides, respectively. Created in BioRender. M. Filippi (2025) https://BioRender.com/87dompp . ( E ) Scheme of the printing sequence to generate the interface and microscopic picture of the muscle-tendon interface (culture day 15), revealing the interdigitated architecture joining the muscle and fibroblast-seeded tissues and texture variance of microscopic pictures quantified in the muscle, interface, and anchor areas of the constructs ( n = 8). The blue dashed line indicates the interdigitated pattern of the interface, and the black arrow indicates the radius of the invagination ( r i ). P values are as follows: 0.002 (muscle versus tendon), 0.002 (tendon versus interface), and 0.461 (muscle versus interface). ( F ) Representative pictures of the different MTU areas showing a different matrix texture. ( G ) Calcium imaging of the different regions of the MTU and controls. Red arrows indicate activated myotubes, and yellow dashed lines indicate the interface border between the two tissues, as determined by the manual positioning of the microscope. Orange and red asterisks indicate the muscle and tendon sides, respectively. Statistical significance is expressed as follows: ** P < 0.01.
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    Image Search Results


    ( A ) Stereoscopic microscopy of the MTU at different time points of the tissue development process. ( B ) Culture conditions for muscle tissue maturation, accounting for culture in growth medium for 4 days and myogenic differentiation medium for 11 days after mounting on the tissue maturation template under mechanical tension. H&E staining ( C ) and confocal imaging ( D ) of the muscle tissue, tendon-muscle interface, and tendon structure on day 15. In (C), red arrowheads indicate myotubes. In (D), the yellow dashed line represents the interface border between the two tissues, as determined by manual positioning of the microscope. Orange and red asterisks indicate the muscle and tendon sides, respectively. Created in BioRender. M. Filippi (2025) https://BioRender.com/87dompp . ( E ) Scheme of the printing sequence to generate the interface and microscopic picture of the muscle-tendon interface (culture day 15), revealing the interdigitated architecture joining the muscle and fibroblast-seeded tissues and texture variance of microscopic pictures quantified in the muscle, interface, and anchor areas of the constructs ( n = 8). The blue dashed line indicates the interdigitated pattern of the interface, and the black arrow indicates the radius of the invagination ( r i ). P values are as follows: 0.002 (muscle versus tendon), 0.002 (tendon versus interface), and 0.461 (muscle versus interface). ( F ) Representative pictures of the different MTU areas showing a different matrix texture. ( G ) Calcium imaging of the different regions of the MTU and controls. Red arrows indicate activated myotubes, and yellow dashed lines indicate the interface border between the two tissues, as determined by the manual positioning of the microscope. Orange and red asterisks indicate the muscle and tendon sides, respectively. Statistical significance is expressed as follows: ** P < 0.01.

    Journal: Science Advances

    Article Title: Multicellular muscle-tendon bioprinting of mechanically optimized musculoskeletal bioactuators with enhanced force transmission

    doi: 10.1126/sciadv.adv2628

    Figure Lengend Snippet: ( A ) Stereoscopic microscopy of the MTU at different time points of the tissue development process. ( B ) Culture conditions for muscle tissue maturation, accounting for culture in growth medium for 4 days and myogenic differentiation medium for 11 days after mounting on the tissue maturation template under mechanical tension. H&E staining ( C ) and confocal imaging ( D ) of the muscle tissue, tendon-muscle interface, and tendon structure on day 15. In (C), red arrowheads indicate myotubes. In (D), the yellow dashed line represents the interface border between the two tissues, as determined by manual positioning of the microscope. Orange and red asterisks indicate the muscle and tendon sides, respectively. Created in BioRender. M. Filippi (2025) https://BioRender.com/87dompp . ( E ) Scheme of the printing sequence to generate the interface and microscopic picture of the muscle-tendon interface (culture day 15), revealing the interdigitated architecture joining the muscle and fibroblast-seeded tissues and texture variance of microscopic pictures quantified in the muscle, interface, and anchor areas of the constructs ( n = 8). The blue dashed line indicates the interdigitated pattern of the interface, and the black arrow indicates the radius of the invagination ( r i ). P values are as follows: 0.002 (muscle versus tendon), 0.002 (tendon versus interface), and 0.461 (muscle versus interface). ( F ) Representative pictures of the different MTU areas showing a different matrix texture. ( G ) Calcium imaging of the different regions of the MTU and controls. Red arrows indicate activated myotubes, and yellow dashed lines indicate the interface border between the two tissues, as determined by the manual positioning of the microscope. Orange and red asterisks indicate the muscle and tendon sides, respectively. Statistical significance is expressed as follows: ** P < 0.01.

    Article Snippet: Calcein and propidium iodide were excited at 488- and 561-nm laser wavelengths, respectively, and imaged on a confocal microscope (Zeiss LSM 780 Airyscan, Zeiss AxioObserver.Z1).

    Techniques: Microscopy, Staining, Imaging, Sequencing, Construct