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lsm 880 axio inverted laser scanning confocal microscope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss lsm 880 axio inverted laser scanning confocal microscope
    Lsm 880 Axio Inverted Laser Scanning 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+880+laser+scanning+microscope/Primovert+Compact+Inverted+Microscope/bio_rxiv__64898__2026__02__11__705362-367-6-5
    Average 99 stars, based on 2152 article reviews
    lsm 880 axio inverted laser scanning confocal microscope - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Laser-Scanning Microscopy:

    Article Title: Tracking the genome-wide occupancy of Arabidopsis LEAFY COTYLEDON1 in endosperm development.
    Article Snippet: .. Confocal images were taken using a Zeiss LSM 880 laser scanning microscope with the following setting of excitation/emission wavelengths: DAPI (405/420-480 nm), GFP (488/505-530 nm), and mCherry (543/550- 650 nm). .. Confocal images were analyzed using the imaging software: LSM Image Browser and Fiji ImageJ software.

    Article Title: Activation and maturation of antigen-specific B cells in nonectopic lung infiltrates are independent of germinal center reactions in the draining lymph node.
    Article Snippet: .. Images were captured on a Carl Zeiss (Oberkochen, Germany) LSM 880 laser scanning microscope with ZEN 2.3 software. ..

    Article Title: Common Gene Networks Orchestrate Organelle Architecture and Inter-Organelle Metabolic Flows for Mucin Production in High Endothelial and Goblet Cells
    Article Snippet: .. Imaging was performed using a Zeiss LSM 880 laser scanning microscope and a Nikon ECLIPSE Ti2 microscope. .. The parameter characterization and quantification of images were analyzed in Imaris 9.1.

    Article Title: CD22 modulation alleviates amyloid β-induced neuroinflammation
    Article Snippet: Activation of MDMi was examined with anti-IbaI antibody (FujiFilm Wako, 019-19741). .. Confocal image acquisition was performed using a Zeiss LSM 880 laser scanning microscope (Carl Zeiss) and images were analyzed with ImageJ software. .. MDMi was treated with designated concentration of soluble CD22 as stated in the Figure for 30 min. MDMi lysate was collected with 1xRIPA lysis buffer (Millipore, 20–188) supplemented with protease and phosphatase inhibitors (Thermo Scientific, 1861281).

    Article Title: Supporting Information for Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics
    Article Snippet: Primary and secondary antibodies used in this study were rabbit anti-g-tubulin (1:500, Sigma-Aldrich #T5192) mouse anti-b-catenin (1:500, Millpore #), mouse anti-acetylated a tubulin (1:1000, Sigma Aldrich #), rabbit anti-mCherry (1:5,000, Abcam, #167453), chicken anti-GFP (1:3,000, Abcam, #ab13970), rabbit anti-ARL13B (1:500, ProteinTech, #17711-1-AP). (1:200, Jackson ImmunoResearch Labs, #103-545-155; RRID: AB 2337390), and Alexa Fluor 647 conjugated goat anti-rabbit IgG (1:200, Jackson ImmunoResearch Labs, #111-605-144). .. Confocal images acquired using a Zeiss LSM 880 laser scanning microscope (Zeiss) were analyzed for basal body clusters. ..

    Article Title: Group B Streptococci lyse endothelial cells to infect the brain in a zebrafish meningitis model.
    Article Snippet: Live confocal imaging and image analysis For confocal imaging, larvae were embedded in 1.2% low melting-point agarose (Fisher Scientific, Cat# 15-455- 202) in a glass bottom plastic dish (WilCo, Cat# GWST-5030) and immersed in water containing 2.8% Syncaine [112]. .. A series of z stack images with a 0.82–1 μm step size were generated through the brain using the Zeiss LSM 880 laser scanning microscope with an LD C-Apochromat 40× objective. .. Imaris (Bitplane Scientific Software) was used to measure fluorescence intensity and construct three-dimensional surface renderings [113].

    Article Title: Dual-phoretic wireless device for directionally oriented and carrier-free targeted drug delivery.
    Article Snippet: .. Also, the resected tumors were fixed, and the nucleus was stained with 4′,6- diamidino- 2- phenylindole to measure the deep tissue penetration using Zeiss LSM 880 laser scanning microscope (W Plan- Apochromat 10×/0.5 M27 working distance = 3.7 mm). ..

    Article Title: Common Gene Networks Orchestrate Organelle Architecture and Inter-Organelle Metabolic Flows for Mucin Production in High Endothelial and Goblet Cells
    Article Snippet: .. Imaging was performed using an LSM 880 laser scanning microscope (Zeiss) and an ECLIPSE Ti2 microscope (Nikon). ..

    Software:

    Article Title: Activation and maturation of antigen-specific B cells in nonectopic lung infiltrates are independent of germinal center reactions in the draining lymph node.
    Article Snippet: .. Images were captured on a Carl Zeiss (Oberkochen, Germany) LSM 880 laser scanning microscope with ZEN 2.3 software. ..

    Imaging:

    Article Title: Common Gene Networks Orchestrate Organelle Architecture and Inter-Organelle Metabolic Flows for Mucin Production in High Endothelial and Goblet Cells
    Article Snippet: .. Imaging was performed using a Zeiss LSM 880 laser scanning microscope and a Nikon ECLIPSE Ti2 microscope. .. The parameter characterization and quantification of images were analyzed in Imaris 9.1.

    Article Title: Common Gene Networks Orchestrate Organelle Architecture and Inter-Organelle Metabolic Flows for Mucin Production in High Endothelial and Goblet Cells
    Article Snippet: .. Imaging was performed using an LSM 880 laser scanning microscope (Zeiss) and an ECLIPSE Ti2 microscope (Nikon). ..

    Microscopy:

    Article Title: Common Gene Networks Orchestrate Organelle Architecture and Inter-Organelle Metabolic Flows for Mucin Production in High Endothelial and Goblet Cells
    Article Snippet: .. Imaging was performed using a Zeiss LSM 880 laser scanning microscope and a Nikon ECLIPSE Ti2 microscope. .. The parameter characterization and quantification of images were analyzed in Imaris 9.1.

    Article Title: Common Gene Networks Orchestrate Organelle Architecture and Inter-Organelle Metabolic Flows for Mucin Production in High Endothelial and Goblet Cells
    Article Snippet: .. Imaging was performed using an LSM 880 laser scanning microscope (Zeiss) and an ECLIPSE Ti2 microscope (Nikon). ..

    Confocal:

    Article Title: CD22 modulation alleviates amyloid β-induced neuroinflammation
    Article Snippet: Activation of MDMi was examined with anti-IbaI antibody (FujiFilm Wako, 019-19741). .. Confocal image acquisition was performed using a Zeiss LSM 880 laser scanning microscope (Carl Zeiss) and images were analyzed with ImageJ software. .. MDMi was treated with designated concentration of soluble CD22 as stated in the Figure for 30 min. MDMi lysate was collected with 1xRIPA lysis buffer (Millipore, 20–188) supplemented with protease and phosphatase inhibitors (Thermo Scientific, 1861281).

    Article Title: Supporting Information for Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics
    Article Snippet: Primary and secondary antibodies used in this study were rabbit anti-g-tubulin (1:500, Sigma-Aldrich #T5192) mouse anti-b-catenin (1:500, Millpore #), mouse anti-acetylated a tubulin (1:1000, Sigma Aldrich #), rabbit anti-mCherry (1:5,000, Abcam, #167453), chicken anti-GFP (1:3,000, Abcam, #ab13970), rabbit anti-ARL13B (1:500, ProteinTech, #17711-1-AP). (1:200, Jackson ImmunoResearch Labs, #103-545-155; RRID: AB 2337390), and Alexa Fluor 647 conjugated goat anti-rabbit IgG (1:200, Jackson ImmunoResearch Labs, #111-605-144). .. Confocal images acquired using a Zeiss LSM 880 laser scanning microscope (Zeiss) were analyzed for basal body clusters. ..

    Generated:

    Article Title: Group B Streptococci lyse endothelial cells to infect the brain in a zebrafish meningitis model.
    Article Snippet: Live confocal imaging and image analysis For confocal imaging, larvae were embedded in 1.2% low melting-point agarose (Fisher Scientific, Cat# 15-455- 202) in a glass bottom plastic dish (WilCo, Cat# GWST-5030) and immersed in water containing 2.8% Syncaine [112]. .. A series of z stack images with a 0.82–1 μm step size were generated through the brain using the Zeiss LSM 880 laser scanning microscope with an LD C-Apochromat 40× objective. .. Imaris (Bitplane Scientific Software) was used to measure fluorescence intensity and construct three-dimensional surface renderings [113].

    Staining:

    Article Title: Dual-phoretic wireless device for directionally oriented and carrier-free targeted drug delivery.
    Article Snippet: .. Also, the resected tumors were fixed, and the nucleus was stained with 4′,6- diamidino- 2- phenylindole to measure the deep tissue penetration using Zeiss LSM 880 laser scanning microscope (W Plan- Apochromat 10×/0.5 M27 working distance = 3.7 mm). ..



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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