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high speed confocal microscopy  (Oxford Instruments)


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    Structured Review

    Oxford Instruments high speed confocal microscopy
    High Speed Confocal Microscopy, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 2819 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/high+speed+confocal+microscopy/Dragonfly/pm41678331-288-5-8
    Average 99 stars, based on 2819 article reviews
    high speed confocal microscopy - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Confocal Microscopy:

    Article Title: TBK1 phagosomal recruitment enhances antifungal immunity via positive feedback regulation with SRC.
    Article Snippet: .. Cells were mounted on slides with nail polish and observed under high-speed confocal microscopy (Andor Dragonfly 200). ..

    Article Title: Remote ischemic preconditioning prevents high‐altitude cerebral edema by enhancing glucose metabolic reprogramming
    Article Snippet: .. Cultured neurons infected with iATPSnFR were stained with MAP2 using immunofluorescence and imaged with high‐speed confocal microscopy (Andor Dragonfly 200). .. The ATP levels, indicated by the fluorescence intensity of iATPSnFR, were quantified using the ImageJ software (NIH).

    Article Title: Remote ischemic preconditioning prevents high‐altitude cerebral edema by enhancing glucose metabolic reprogramming
    Article Snippet: The coverslips were then mounted with ProLongTM Glass Antifade Mountant with or without NucBlueTM Stain (Invitrogen). .. All images were captured using high‐speed confocal microscopy (Andor Dragonfly 200). .. TUNEL was performed following the standard protocols provided in the manual of the In Situ Cell Death Detection Kit (Cat. No. 11684817910, Roche).

    Article Title: Triglycerides induce endoplasmic reticulum lipid bilayer stress to activate PERK and enhance antifungal immunity.
    Article Snippet: .. Sealed slides were analyzed using high-speed confocal microscopy (Andor Dragonfly 200) with companion software. ..

    Article Title: Lipid droplets restrict phagosome formation in antifungal immunity.
    Article Snippet: Lipid droplets (LDs) are intracellular organelles that can be induced and interact with phagosomes during the process of pathogen phagocytosis in macrophages.. However, the function of LDs in phagocytosis remains elusive.. Here, we unveil the role of LDs in modulating phagosome formation via a fungal infection model.

    Article Title: MSCs act as biopatches for blood-retinal barrier preservation to enhance functional recovery after retinal I/R
    Article Snippet: Retinal sections were fixed in 4% PFA for 20 min, permeabilized in 0.15% Triton X-100 for 15 min, and blocked with PBS-5% normal goat serum (BOSTER, Pleasanton, CA, USA) for 1 h. Both whole-mounted neural retinas and retinal sections were incubated with appropriate primary and secondary antibodies. .. Images were captured using Dragonfly high-speed confocal microscopy (ANDOR, Oxford Instruments, Oxford, UK). ..

    Article Title: Lipid droplets restrict phagosome formation during Candida challenge
    Article Snippet: .. Sealed slides were analyzed using high-speed confocal microscopy (Andor Dragonfly 200) with companion software. ..

    Cell Culture:

    Article Title: Remote ischemic preconditioning prevents high‐altitude cerebral edema by enhancing glucose metabolic reprogramming
    Article Snippet: .. Cultured neurons infected with iATPSnFR were stained with MAP2 using immunofluorescence and imaged with high‐speed confocal microscopy (Andor Dragonfly 200). .. The ATP levels, indicated by the fluorescence intensity of iATPSnFR, were quantified using the ImageJ software (NIH).

    Infection:

    Article Title: Remote ischemic preconditioning prevents high‐altitude cerebral edema by enhancing glucose metabolic reprogramming
    Article Snippet: .. Cultured neurons infected with iATPSnFR were stained with MAP2 using immunofluorescence and imaged with high‐speed confocal microscopy (Andor Dragonfly 200). .. The ATP levels, indicated by the fluorescence intensity of iATPSnFR, were quantified using the ImageJ software (NIH).

    Staining:

    Article Title: Remote ischemic preconditioning prevents high‐altitude cerebral edema by enhancing glucose metabolic reprogramming
    Article Snippet: .. Cultured neurons infected with iATPSnFR were stained with MAP2 using immunofluorescence and imaged with high‐speed confocal microscopy (Andor Dragonfly 200). .. The ATP levels, indicated by the fluorescence intensity of iATPSnFR, were quantified using the ImageJ software (NIH).

    Immunofluorescence:

    Article Title: Remote ischemic preconditioning prevents high‐altitude cerebral edema by enhancing glucose metabolic reprogramming
    Article Snippet: .. Cultured neurons infected with iATPSnFR were stained with MAP2 using immunofluorescence and imaged with high‐speed confocal microscopy (Andor Dragonfly 200). .. The ATP levels, indicated by the fluorescence intensity of iATPSnFR, were quantified using the ImageJ software (NIH).

    Software:

    Article Title: Triglycerides induce endoplasmic reticulum lipid bilayer stress to activate PERK and enhance antifungal immunity.
    Article Snippet: .. Sealed slides were analyzed using high-speed confocal microscopy (Andor Dragonfly 200) with companion software. ..

    Article Title: Lipid droplets restrict phagosome formation in antifungal immunity.
    Article Snippet: Lipid droplets (LDs) are intracellular organelles that can be induced and interact with phagosomes during the process of pathogen phagocytosis in macrophages.. However, the function of LDs in phagocytosis remains elusive.. Here, we unveil the role of LDs in modulating phagosome formation via a fungal infection model.

    Article Title: Lipid droplets restrict phagosome formation during Candida challenge
    Article Snippet: .. Sealed slides were analyzed using high-speed confocal microscopy (Andor Dragonfly 200) with companion software. ..



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    Image Search Results


    ( A ) Par-3 consists of three conserved regions (CRs), the oligomerization domain (CR1), the three PDZ domains (CR2), and the aPKC binding domain (CR3). The predicted AurkA phosphorylation sites are located at Ser 227 and Ser 954 (green), which are conserved across vertebrates. ( B ) Experimental schematic of mRNA injection into one-cell or 16/32-cell stage zebrafish embryos. ( C ) Images of embryonic brain morphology at ~28 hpf. Images were taken at 200× on the Zeiss compound microscope. ( D ) Quantification. Phenotyping rubrics are described in fig. S2. ( E ) Time-lapse sequence of images showing Par-3 and Par-3 phospho mutants (GFP only in the heatmap) in mitotic RGPs at the prophase, metaphase, and telophase. ( F ) Quantification. Relative cytoplasmic Par-3 expression was measured at the prophase, metaphase, and telophase using Fiji. One-way ANOVA test with a post hoc comparison to control (Par-3-GFP). * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001; ns, not significant. For detailed statistics, see table S1. See table S2 for the representative image signal values compared to the median signal values.

    Journal: Science Advances

    Article Title: Phosphorylation by Aurora kinase A facilitates cortical-cytoplasmic dynamics of Par-3 in asymmetric division of radial glia progenitors

    doi: 10.1126/sciadv.adq3858

    Figure Lengend Snippet: ( A ) Par-3 consists of three conserved regions (CRs), the oligomerization domain (CR1), the three PDZ domains (CR2), and the aPKC binding domain (CR3). The predicted AurkA phosphorylation sites are located at Ser 227 and Ser 954 (green), which are conserved across vertebrates. ( B ) Experimental schematic of mRNA injection into one-cell or 16/32-cell stage zebrafish embryos. ( C ) Images of embryonic brain morphology at ~28 hpf. Images were taken at 200× on the Zeiss compound microscope. ( D ) Quantification. Phenotyping rubrics are described in fig. S2. ( E ) Time-lapse sequence of images showing Par-3 and Par-3 phospho mutants (GFP only in the heatmap) in mitotic RGPs at the prophase, metaphase, and telophase. ( F ) Quantification. Relative cytoplasmic Par-3 expression was measured at the prophase, metaphase, and telophase using Fiji. One-way ANOVA test with a post hoc comparison to control (Par-3-GFP). * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001; ns, not significant. For detailed statistics, see table S1. See table S2 for the representative image signal values compared to the median signal values.

    Article Snippet: In vivo time-lapse imaging was done using a confocal microscope (Nikon CSU-W1 Spinning Disk/High Speed Widefield confocal microscopy and Weill CSU-W1 SoRA Spinning Disk Confocal) with a 40× water immersion objective.

    Techniques: Binding Assay, Phospho-proteomics, Injection, Microscopy, Sequencing, Expressing, Comparison, Control