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confocal laser scanning microscope lsm880 airyscan with stedycon  (Carl Zeiss)


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    Structured Review

    Carl Zeiss confocal laser scanning microscope lsm880 airyscan with stedycon
    Confocal Laser Scanning Microscope Lsm880 Airyscan With Stedycon, 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/stedycon/880+confocal+lsm+microscope/pm40527084-59-7-6
    Average 90 stars, based on 1 article reviews
    confocal laser scanning microscope lsm880 airyscan with stedycon - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    other:

    Article Title: Targeting olfactory receptor OR2AT4: An innovative aptamer-based treatment for hair growth promotion
    Article Snippet: Analyses were performed using Leica DM5000B and Zeiss LSM 880 microscopes.

    Article Title: Dual crosslinking approach of K + and TGase to enhance the thermal stability and intestinal delivery efficiency of emulsion gels.
    Article Snippet: s. This study aimed to develop a dual-network interpenetrating emulsion gels (EGs) by dual crosslinking κ-carrageenan and gelatin with K and transglutaminase (TGase) to enhance its thermal stability, and use β-carotene as a model to enhance its chemical stability and intestinal delivery.. Thermal stability of EGs was improved in two aspects: first, the hardness and chewiness reached their maximum values, with a 121.65 kPa mechanical strength to resist external forces; second, improvement in 45.77 % swelling property and 95.3 % water retention.. Dual-network EGs possessed excellent elasticity, uniform and stable thermal resistance.


    Fluorescence:

    Article Title: 3D printing of mycelium-enhanced plant-based protein composites for customizable texture in meat analogues
    Article Snippet: Mycelium-based composites are extraordinary functional materials with vast potential in food applications.. This study presents a novel approach to developing meat analogues using mycelium-enhanced plant proteinpolysaccharide hydrocolloids (containing k-carrageenan and locust bean gum), fabricated through 3D printing.. By leveraging mycelium as a biological adhesive, we achieved enhanced structural stability, elasticity, and mechanical anisotropy, alongside a unique fibrous texture mimicking the tearing effect of meat.

    Article Title: Microwave-assisted immunostaining for rapid labeling of matrix-embedded multicellular structures
    Article Snippet: .. Fluorescence image acquisition was performed by a confocal laser scanning microscope (Zeiss LSM 880 with Airyscan, Zeiss, Oberkochen, Baden-Württemberg, Germany). .. A 40× Plan-Apochromat 1.2 NA water immersion objective (Zeiss) was used for imaging spheroids.

    Laser-Scanning Microscopy:

    Article Title: 3D printing of mycelium-enhanced plant-based protein composites for customizable texture in meat analogues
    Article Snippet: Mycelium-based composites are extraordinary functional materials with vast potential in food applications.. This study presents a novel approach to developing meat analogues using mycelium-enhanced plant proteinpolysaccharide hydrocolloids (containing k-carrageenan and locust bean gum), fabricated through 3D printing.. By leveraging mycelium as a biological adhesive, we achieved enhanced structural stability, elasticity, and mechanical anisotropy, alongside a unique fibrous texture mimicking the tearing effect of meat.

    Article Title: Microwave-assisted immunostaining for rapid labeling of matrix-embedded multicellular structures
    Article Snippet: .. Fluorescence image acquisition was performed by a confocal laser scanning microscope (Zeiss LSM 880 with Airyscan, Zeiss, Oberkochen, Baden-Württemberg, Germany). .. A 40× Plan-Apochromat 1.2 NA water immersion objective (Zeiss) was used for imaging spheroids.

    Second Harmonic Generation Microscopy:

    Article Title: Microwave-assisted immunostaining for rapid labeling of matrix-embedded multicellular structures
    Article Snippet: .. Second harmonic generation (SHG) imaging was performed to visualize the collagen fibers in the hydrogels on the Zeiss LSM 880 which contained an added tunable Ti:sapphire laser (100 fs, 80 MHz; Coherent, Santa Clara, CA). ..

    Imaging:

    Article Title: Microwave-assisted immunostaining for rapid labeling of matrix-embedded multicellular structures
    Article Snippet: .. Second harmonic generation (SHG) imaging was performed to visualize the collagen fibers in the hydrogels on the Zeiss LSM 880 which contained an added tunable Ti:sapphire laser (100 fs, 80 MHz; Coherent, Santa Clara, CA). ..

    Infection:

    Article Title: Influence of the ATP-dependent DNA ligase, Lig E, on Neisseria gonorrhoeae microcolony and biofilm formation
    Article Snippet: Biofilms grown on polycarbonate coupons were visualised using the Zeiss Cell Discoverer 7 microscope at ×40 (objective) magnification using the suGFP channel (laser excitation (exc) wavelength: 480 nm, laser emission wavelength (em): 505 nm) to image the sfGFP-expressing gonococcal cells. .. Infected rHVE tissues were visualised using the Zeiss LSM 880 with Airyscan microscope at ×63 magnification. ..

    Article Title: The function of BoVDAC3 from broccoli in oxidative stress response and programmed cell death in BY-2 cells
    Article Snippet: Voltage dependent anion channel protein (VDAC) had been shown to played a critical role in programmed cell death (PCD).. However, the functional role of BoVDAC3 in oxidative stress response and PCD process of postharvest broccoli remains unclear.. In this study, BoVDAC3 was overexpressed in tobacco bright yellow-2 (BY-2) cells to investigate its function.

    Microscopy:

    Article Title: Influence of the ATP-dependent DNA ligase, Lig E, on Neisseria gonorrhoeae microcolony and biofilm formation
    Article Snippet: Biofilms grown on polycarbonate coupons were visualised using the Zeiss Cell Discoverer 7 microscope at ×40 (objective) magnification using the suGFP channel (laser excitation (exc) wavelength: 480 nm, laser emission wavelength (em): 505 nm) to image the sfGFP-expressing gonococcal cells. .. Infected rHVE tissues were visualised using the Zeiss LSM 880 with Airyscan microscope at ×63 magnification. ..

    Article Title: The function of BoVDAC3 from broccoli in oxidative stress response and programmed cell death in BY-2 cells
    Article Snippet: Voltage dependent anion channel protein (VDAC) had been shown to played a critical role in programmed cell death (PCD).. However, the functional role of BoVDAC3 in oxidative stress response and PCD process of postharvest broccoli remains unclear.. In this study, BoVDAC3 was overexpressed in tobacco bright yellow-2 (BY-2) cells to investigate its function.

    Confocal:

    Article Title: Microwave-assisted immunostaining for rapid labeling of matrix-embedded multicellular structures
    Article Snippet: .. Fluorescence image acquisition was performed by a confocal laser scanning microscope (Zeiss LSM 880 with Airyscan, Zeiss, Oberkochen, Baden-Württemberg, Germany). .. A 40× Plan-Apochromat 1.2 NA water immersion objective (Zeiss) was used for imaging spheroids.



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    Carl Zeiss confocal laser scanning microscope lsm880 airyscan with stedycon
    (A) Representative FACS plot of cell sorting strategy to isolate purified oxLDL + and oxLDL - neutrophils. ( B ) Reactome pathway analysis of proteins increased in oxLDL + subset in the proteomics data. ( C ) Heatmap of selected differentially expressed proteins in oxLDL - and oxLDL + neutrophil populations. ( D ) 100x <t>STED</t> immunofluorescent imaging of peritoneal cells isolated from zymosan and oxLDL-Dil IP-injected mice and stained for phalloidin. Cells were also stained and checked for Ly6G expression, which is not shown for clarity of phalloidin stain. Representative oxLDL + (left) and oxLDL - (right) cells are shown. ( E ) In vitro oxLDL-Dil uptake in bone marrow enriched neutrophils treated with cytochalasin D. ( F ) Transwell migration assay of oxLDL - and oxLDL + neutrophils sorted from peritoneal cells following zymosan and oxLDL-Dil IP injection. ( E-F ) All symbols represent independent experiments. Data are expressed as mean ± SEM. Statistical differences were calculated by one-way ANOVA for F and two-way ANOVA for G. * ≤ 0.05, ** ≤ 0.01,***≤0.001
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    Image Search Results


    (A) Representative FACS plot of cell sorting strategy to isolate purified oxLDL + and oxLDL - neutrophils. ( B ) Reactome pathway analysis of proteins increased in oxLDL + subset in the proteomics data. ( C ) Heatmap of selected differentially expressed proteins in oxLDL - and oxLDL + neutrophil populations. ( D ) 100x STED immunofluorescent imaging of peritoneal cells isolated from zymosan and oxLDL-Dil IP-injected mice and stained for phalloidin. Cells were also stained and checked for Ly6G expression, which is not shown for clarity of phalloidin stain. Representative oxLDL + (left) and oxLDL - (right) cells are shown. ( E ) In vitro oxLDL-Dil uptake in bone marrow enriched neutrophils treated with cytochalasin D. ( F ) Transwell migration assay of oxLDL - and oxLDL + neutrophils sorted from peritoneal cells following zymosan and oxLDL-Dil IP injection. ( E-F ) All symbols represent independent experiments. Data are expressed as mean ± SEM. Statistical differences were calculated by one-way ANOVA for F and two-way ANOVA for G. * ≤ 0.05, ** ≤ 0.01,***≤0.001

    Journal: bioRxiv

    Article Title: Neutrophil TLR2 signaling promotes lipid accumulation and vascular plaque growth

    doi: 10.1101/2025.07.09.663961

    Figure Lengend Snippet: (A) Representative FACS plot of cell sorting strategy to isolate purified oxLDL + and oxLDL - neutrophils. ( B ) Reactome pathway analysis of proteins increased in oxLDL + subset in the proteomics data. ( C ) Heatmap of selected differentially expressed proteins in oxLDL - and oxLDL + neutrophil populations. ( D ) 100x STED immunofluorescent imaging of peritoneal cells isolated from zymosan and oxLDL-Dil IP-injected mice and stained for phalloidin. Cells were also stained and checked for Ly6G expression, which is not shown for clarity of phalloidin stain. Representative oxLDL + (left) and oxLDL - (right) cells are shown. ( E ) In vitro oxLDL-Dil uptake in bone marrow enriched neutrophils treated with cytochalasin D. ( F ) Transwell migration assay of oxLDL - and oxLDL + neutrophils sorted from peritoneal cells following zymosan and oxLDL-Dil IP injection. ( E-F ) All symbols represent independent experiments. Data are expressed as mean ± SEM. Statistical differences were calculated by one-way ANOVA for F and two-way ANOVA for G. * ≤ 0.05, ** ≤ 0.01,***≤0.001

    Article Snippet: For super resolution imaging, slides were imaged using a four detector Abberior STEDYCON STED unit.

    Techniques: FACS, Purification, Imaging, Isolation, Injection, Staining, Expressing, In Vitro, Transwell Migration Assay