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zeiss 880 confocal microscope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss zeiss 880 confocal microscope
    Zeiss 880 Confocal Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 1752 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/880+confocal+microscope/Primovert+Compact+Inverted+Microscope/pm41764735-72-11-11
    Average 99 stars, based on 1752 article reviews
    zeiss 880 confocal microscope - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Immunolabeling:

    Article Title: Transgene cassettes designed to express a human MECP2 gene
    Article Snippet: Immunolabeled sections were imaged with a Zeiss 880 confocal microscope using Zen software at UT Southwestern's Live Cell Imaging Facility. .. Immunolabeled sections were imaged with a Zeiss 880 confocal microscope using Zen software at UT Southwestern's Live Cell Imaging Facility. ..

    Microscopy:

    Article Title: Transgene cassettes designed to express a human MECP2 gene
    Article Snippet: Immunolabeled sections were imaged with a Zeiss 880 confocal microscope using Zen software at UT Southwestern's Live Cell Imaging Facility. .. Immunolabeled sections were imaged with a Zeiss 880 confocal microscope using Zen software at UT Southwestern's Live Cell Imaging Facility. ..

    Article Title: Brain-wide connectivity patterns of feedforward and feedback cortico-cortical neurons in the mouse secondary visual cortex
    Article Snippet: All sections were scanned with a 10x/0.45 NA (wd-2.0 mm) objective on a Zeiss AxioImager Z2 Widefield Microscope using tile scan and Z-stack (every 6-8 μm). .. Representative images were taken with the Zeiss 880 Confocal Microscope with 10x/0.45 NA (wd-2.0 mm) or 40x/ 0.95 NA corr (wd-0.25 mm) objectives. .. Scanned images were first processed in Zeiss ZEN 3.11 with DAPI images for alignment and fluorescent images for eGFP+ or mCherry+ cell detections exported for processing.

    Article Title: SORLA upregulation suppresses global pathological effects in aged tauopathy mouse brain
    Article Snippet: .. All samples were stained concurrently and images were acquired using a Zeiss 880 Confocal Microscope at 63x magnification. ..

    Article Title: Histone H3 N-terminal recognition by the PHD finger of PHRF1 is required for proper DNA damage response
    Article Snippet: .. For purposes of visualization, confocal images were acquired on a Zeiss 880 confocal microscope using a Plan-Apo 20×/0.8 WD 0.55mm at 4× zoom. .. Z-stacks of 0.9 μm slices were taken and maximum intensity projections were made in ImageJ for display.

    Article Title: De novo assembly of RNA m 6 A modification factors into viral genome-associated nuclear bodies drives HCMV RNA accumulation.
    Article Snippet: Published by Elsevier Inc. 1 This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). ll OPEN ACCESS (A) NHDFs either uninfected or infected with HCMV Ad169-GFP were fixed at the indicated times (hpi) and the subcellular distribution of WTAP or YTHDC1 was visualized by indirect IF using a Leica CTR5000 epifluorescent microscope. .. Nuclei were identified by DAPI staining (blue in merged image) and HCMV-positive cells by GFP fluorescence. (B) NHDFs infected as in (A), except cells were fixed at 6 hpi, probed simultaneously with WTAP and YTHDC1 antibodies and visualized using a Zeiss 880 confocal microscope. (legend continued on next page) 2 Cell Reports 44, 115826, July 22, 2025 survival. ..

    Article Title: TUG protein acts through a disordered region to organize the early secretory pathway
    Article Snippet: .. Images were acquired on a Zeiss 880 confocal microscope, and z-stacks collapsed to draw regions outlining Golgi staining. ..

    Article Title: Symbiotic entrenchment through ecological Catch-22
    Article Snippet: .. Samples were mounted together and imaged on a Zeiss 880 confocal microscope (Zeiss, Germany) in Airyscan fast mode using identical imaging parameters. ..

    Software:

    Article Title: Transgene cassettes designed to express a human MECP2 gene
    Article Snippet: Immunolabeled sections were imaged with a Zeiss 880 confocal microscope using Zen software at UT Southwestern's Live Cell Imaging Facility. .. Immunolabeled sections were imaged with a Zeiss 880 confocal microscope using Zen software at UT Southwestern's Live Cell Imaging Facility. ..

    Live Cell Imaging:

    Article Title: Transgene cassettes designed to express a human MECP2 gene
    Article Snippet: Immunolabeled sections were imaged with a Zeiss 880 confocal microscope using Zen software at UT Southwestern's Live Cell Imaging Facility. .. Immunolabeled sections were imaged with a Zeiss 880 confocal microscope using Zen software at UT Southwestern's Live Cell Imaging Facility. ..

    Staining:

    Article Title: SORLA upregulation suppresses global pathological effects in aged tauopathy mouse brain
    Article Snippet: .. All samples were stained concurrently and images were acquired using a Zeiss 880 Confocal Microscope at 63x magnification. ..

    Article Title: De novo assembly of RNA m 6 A modification factors into viral genome-associated nuclear bodies drives HCMV RNA accumulation.
    Article Snippet: Published by Elsevier Inc. 1 This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). ll OPEN ACCESS (A) NHDFs either uninfected or infected with HCMV Ad169-GFP were fixed at the indicated times (hpi) and the subcellular distribution of WTAP or YTHDC1 was visualized by indirect IF using a Leica CTR5000 epifluorescent microscope. .. Nuclei were identified by DAPI staining (blue in merged image) and HCMV-positive cells by GFP fluorescence. (B) NHDFs infected as in (A), except cells were fixed at 6 hpi, probed simultaneously with WTAP and YTHDC1 antibodies and visualized using a Zeiss 880 confocal microscope. (legend continued on next page) 2 Cell Reports 44, 115826, July 22, 2025 survival. ..

    Article Title: TUG protein acts through a disordered region to organize the early secretory pathway
    Article Snippet: .. Images were acquired on a Zeiss 880 confocal microscope, and z-stacks collapsed to draw regions outlining Golgi staining. ..

    Fluorescence:

    Article Title: De novo assembly of RNA m 6 A modification factors into viral genome-associated nuclear bodies drives HCMV RNA accumulation.
    Article Snippet: Published by Elsevier Inc. 1 This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). ll OPEN ACCESS (A) NHDFs either uninfected or infected with HCMV Ad169-GFP were fixed at the indicated times (hpi) and the subcellular distribution of WTAP or YTHDC1 was visualized by indirect IF using a Leica CTR5000 epifluorescent microscope. .. Nuclei were identified by DAPI staining (blue in merged image) and HCMV-positive cells by GFP fluorescence. (B) NHDFs infected as in (A), except cells were fixed at 6 hpi, probed simultaneously with WTAP and YTHDC1 antibodies and visualized using a Zeiss 880 confocal microscope. (legend continued on next page) 2 Cell Reports 44, 115826, July 22, 2025 survival. ..

    Infection:

    Article Title: De novo assembly of RNA m 6 A modification factors into viral genome-associated nuclear bodies drives HCMV RNA accumulation.
    Article Snippet: Published by Elsevier Inc. 1 This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). ll OPEN ACCESS (A) NHDFs either uninfected or infected with HCMV Ad169-GFP were fixed at the indicated times (hpi) and the subcellular distribution of WTAP or YTHDC1 was visualized by indirect IF using a Leica CTR5000 epifluorescent microscope. .. Nuclei were identified by DAPI staining (blue in merged image) and HCMV-positive cells by GFP fluorescence. (B) NHDFs infected as in (A), except cells were fixed at 6 hpi, probed simultaneously with WTAP and YTHDC1 antibodies and visualized using a Zeiss 880 confocal microscope. (legend continued on next page) 2 Cell Reports 44, 115826, July 22, 2025 survival. ..

    other:

    Article Title: Identification of functional non-coding variants associated with orofacial cleft
    Article Snippet: Images were collected with Zeiss 880 or 980 confocal microscopes using the ZEN software (Zeiss).

    Imaging:

    Article Title: Symbiotic entrenchment through ecological Catch-22
    Article Snippet: .. Samples were mounted together and imaged on a Zeiss 880 confocal microscope (Zeiss, Germany) in Airyscan fast mode using identical imaging parameters. ..



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    Image Search Results


    The motility of C. elegans expressing myo-3p::myo-3::gfp was assessed on day 4 of adulthood following two generations of control RNAi (L4440) via feeding. Nematodes were synchronized by egg laying and recorded in M9 media after 30-s acclimation. Videos were acquired at 7.8× magnification and 25 fps using a Leica M205FA stereo microscope. Motility, measured as body bends per second (BBPS), was quantified using WormLab software .

    Journal: The Journal of Cell Biology

    Article Title: Nodal modulator (NOMO) is a force-bearing transmembrane protein required for muscle differentiation

    doi: 10.1083/jcb.202505010

    Figure Lengend Snippet: The motility of C. elegans expressing myo-3p::myo-3::gfp was assessed on day 4 of adulthood following two generations of control RNAi (L4440) via feeding. Nematodes were synchronized by egg laying and recorded in M9 media after 30-s acclimation. Videos were acquired at 7.8× magnification and 25 fps using a Leica M205FA stereo microscope. Motility, measured as body bends per second (BBPS), was quantified using WormLab software .

    Article Snippet: Imaging was performed on an LSM 880 laser scanning confocal microscope (Zeiss) using a C Plan-Apochromat 63×/1.40 oil DIC M27 objective using ZEN 2.1 software (Zeiss) with a stage maintained at 37°C and 5% CO 2 .

    Techniques: Expressing, Control, Microscopy, Software

    The motility of C. elegans expressing myo-3p::myo-3::gfp was evaluated on day 4 of adulthood after two generations of RNAi-targeting nra-4 through feeding. Nematodes were synchronized by egg laying and recorded in M9 media following a 30-s acclimation. Videos were captured at 7.8× magnification and 25 fps using a Leica M205FA stereo microscope. Motility (BBPS) was analyzed using WormLab software .

    Journal: The Journal of Cell Biology

    Article Title: Nodal modulator (NOMO) is a force-bearing transmembrane protein required for muscle differentiation

    doi: 10.1083/jcb.202505010

    Figure Lengend Snippet: The motility of C. elegans expressing myo-3p::myo-3::gfp was evaluated on day 4 of adulthood after two generations of RNAi-targeting nra-4 through feeding. Nematodes were synchronized by egg laying and recorded in M9 media following a 30-s acclimation. Videos were captured at 7.8× magnification and 25 fps using a Leica M205FA stereo microscope. Motility (BBPS) was analyzed using WormLab software .

    Article Snippet: Imaging was performed on an LSM 880 laser scanning confocal microscope (Zeiss) using a C Plan-Apochromat 63×/1.40 oil DIC M27 objective using ZEN 2.1 software (Zeiss) with a stage maintained at 37°C and 5% CO 2 .

    Techniques: Expressing, Microscopy, Software