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axr point scanning confocal microscope  (Nikon)


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    Structured Review

    Nikon axr point scanning confocal microscope
    Axr Point Scanning Confocal Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59714 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/axr+point+scanning+confocal+microscope/Objectives/pmc12999495-374-6-5
    Average 99 stars, based on 59714 article reviews
    axr point scanning confocal microscope - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Fluorescence:

    Article Title: 4D force patterning enables spatial control of angiogenesis
    Article Snippet: .. Fluorescence images were captured on a Nikon AXR point scanning confocal microscope using 4x, 10x, and 20x objectives (Nikon) and processed using the Nikon Denoise.ai software and ImageJ. ..

    Microscopy:

    Article Title: 4D force patterning enables spatial control of angiogenesis
    Article Snippet: .. Fluorescence images were captured on a Nikon AXR point scanning confocal microscope using 4x, 10x, and 20x objectives (Nikon) and processed using the Nikon Denoise.ai software and ImageJ. ..

    Article Title: Hypercholesterolemia drives microglial dysfunction and weakens response to amyloid plaques.
    Article Snippet: They were then incubated with primary antibodies diluted in blocking solution (PBS with 1 % NDS) at 4 ◦C for 24 h, except for PU.1 staining, which was incubated for 48 h. Following primary antibody incubation, sections were incubated with appropriate secondary antibodies at room temperature for 2 h. Sections were mounted on slides with ProLong Diamond (Life Technologies). .. Images were captured on a ZEISS Axio Observer and/or the Nikon AXR point scanning confocal microscope. ..

    Article Title: Paracrine effects of the senescence-associated secretory phenotype decrease cancer cell adhesion
    Article Snippet: Spheroids were then incubated with 300nM DAPI in 0.1% Triton X-100 in TBS for 15 minutes, washed three times with 0.1% Triton X-100 in TBS, mounted with fluorescence mounting medium (9 ml of glycerol [Fisher Scientific cat#BP229-1], 1 ml of 1× PBS, and 10 mg of p-phenylenediamine [EMD Chemicals, cat# PX0730]; pH was adjusted to 8.0–9.0 using carbonate-bicarbonate buffer [0.2 M anhydrous sodium carbonate, 0.2 M sodium bicarbonate]) and sealed. .. Z-stacked images were taken with a Leica Thunder Imager and Nikon AXR point scanning confocal microscope with a 20x objective and processed using ImageJ. ..

    Article Title: The IQGAP-related RasGAP IqgC regulates cell-substratum adhesion in Dictyostelium discoideum.
    Article Snippet: .. The cells were imaged using a Nikon AXR point scanning confocal microscope equipped with a NSPARC detector and a PLAN APO 60×1.30 SIL λS OFN25 DIC N2 objective using an excitation wavelength of 488 nm and a detection range of 502–546 nm at 21 °C. ..

    Article Title: GlycoRNA complexed with heparan sulfate regulates VEGF-A signalling
    Article Snippet: .. Images were acquired using a Nikon AXR point scanning confocal microscope with ×10 and ×20 objectives (Nikon), and z -stack images were processed using the Nikon Denoise.ai software and ImageJ. ..

    Article Title: GlycoRNA complexed with heparan sulfate regulates VEGF-A signalling.
    Article Snippet: .. Images were acquired using a Nikon AXR point scanning confocal microscope with ×10 and ×20 objectives (Nikon), and z-stack images were processed using the Nikon Denoise.ai software and ImageJ. ..

    Software:

    Article Title: 4D force patterning enables spatial control of angiogenesis
    Article Snippet: .. Fluorescence images were captured on a Nikon AXR point scanning confocal microscope using 4x, 10x, and 20x objectives (Nikon) and processed using the Nikon Denoise.ai software and ImageJ. ..

    Article Title: GlycoRNA complexed with heparan sulfate regulates VEGF-A signalling
    Article Snippet: .. Images were acquired using a Nikon AXR point scanning confocal microscope with ×10 and ×20 objectives (Nikon), and z -stack images were processed using the Nikon Denoise.ai software and ImageJ. ..

    Article Title: GlycoRNA complexed with heparan sulfate regulates VEGF-A signalling.
    Article Snippet: .. Images were acquired using a Nikon AXR point scanning confocal microscope with ×10 and ×20 objectives (Nikon), and z-stack images were processed using the Nikon Denoise.ai software and ImageJ. ..



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    (A) Schematic of imaging paradigm used to assess activity-dependent AMPA receptor (GluA1) surface trafficking. Neurons were transfected with SEP-GluA1, extensively photobleached, and <t>fluorescence</t> recovery was measured every 5 min with a confocal <t>microscope.</t> (B) Confocal images of cortical neurons expressing a tRFP cell fill and SEP-GluA1. Bleaching (t=0 min) and fluorescence recovery are shown (t= 5-25min). Scale bar 50 μm (top) and 10 μm (bottom). (C) Fluorescence recovery is reduced in duplication neurons indicating impaired GluA1 insertion (repeated measures two-way ANOVA with Šídák post-hoc test, p = 0.0153). Data are displayed as mean ± s.e.m. *p < 0.05. Abbreviations: WT, 16p11.2 +/+ ; Dup, 16p11.2 dup/+ .
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    (A) Schematic of imaging paradigm used to assess activity-dependent AMPA receptor (GluA1) surface trafficking. Neurons were transfected with SEP-GluA1, extensively photobleached, and <t>fluorescence</t> recovery was measured every 5 min with a confocal <t>microscope.</t> (B) Confocal images of cortical neurons expressing a tRFP cell fill and SEP-GluA1. Bleaching (t=0 min) and fluorescence recovery are shown (t= 5-25min). Scale bar 50 μm (top) and 10 μm (bottom). (C) Fluorescence recovery is reduced in duplication neurons indicating impaired GluA1 insertion (repeated measures two-way ANOVA with Šídák post-hoc test, p = 0.0153). Data are displayed as mean ± s.e.m. *p < 0.05. Abbreviations: WT, 16p11.2 +/+ ; Dup, 16p11.2 dup/+ .
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    (A) Schematic of imaging paradigm used to assess activity-dependent AMPA receptor (GluA1) surface trafficking. Neurons were transfected with SEP-GluA1, extensively photobleached, and <t>fluorescence</t> recovery was measured every 5 min with a confocal <t>microscope.</t> (B) Confocal images of cortical neurons expressing a tRFP cell fill and SEP-GluA1. Bleaching (t=0 min) and fluorescence recovery are shown (t= 5-25min). Scale bar 50 μm (top) and 10 μm (bottom). (C) Fluorescence recovery is reduced in duplication neurons indicating impaired GluA1 insertion (repeated measures two-way ANOVA with Šídák post-hoc test, p = 0.0153). Data are displayed as mean ± s.e.m. *p < 0.05. Abbreviations: WT, 16p11.2 +/+ ; Dup, 16p11.2 dup/+ .
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    (A) Schematic of imaging paradigm used to assess activity-dependent AMPA receptor (GluA1) surface trafficking. Neurons were transfected with SEP-GluA1, extensively photobleached, and <t>fluorescence</t> recovery was measured every 5 min with a confocal <t>microscope.</t> (B) Confocal images of cortical neurons expressing a tRFP cell fill and SEP-GluA1. Bleaching (t=0 min) and fluorescence recovery are shown (t= 5-25min). Scale bar 50 μm (top) and 10 μm (bottom). (C) Fluorescence recovery is reduced in duplication neurons indicating impaired GluA1 insertion (repeated measures two-way ANOVA with Šídák post-hoc test, p = 0.0153). Data are displayed as mean ± s.e.m. *p < 0.05. Abbreviations: WT, 16p11.2 +/+ ; Dup, 16p11.2 dup/+ .
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    Image Search Results


    (A) Schematic of imaging paradigm used to assess activity-dependent AMPA receptor (GluA1) surface trafficking. Neurons were transfected with SEP-GluA1, extensively photobleached, and fluorescence recovery was measured every 5 min with a confocal microscope. (B) Confocal images of cortical neurons expressing a tRFP cell fill and SEP-GluA1. Bleaching (t=0 min) and fluorescence recovery are shown (t= 5-25min). Scale bar 50 μm (top) and 10 μm (bottom). (C) Fluorescence recovery is reduced in duplication neurons indicating impaired GluA1 insertion (repeated measures two-way ANOVA with Šídák post-hoc test, p = 0.0153). Data are displayed as mean ± s.e.m. *p < 0.05. Abbreviations: WT, 16p11.2 +/+ ; Dup, 16p11.2 dup/+ .

    Journal: bioRxiv

    Article Title: Impairment of homeostatic structural plasticity caused by the autism and schizophrenia-associated 16p11.2 duplication

    doi: 10.1101/2025.03.06.641931

    Figure Lengend Snippet: (A) Schematic of imaging paradigm used to assess activity-dependent AMPA receptor (GluA1) surface trafficking. Neurons were transfected with SEP-GluA1, extensively photobleached, and fluorescence recovery was measured every 5 min with a confocal microscope. (B) Confocal images of cortical neurons expressing a tRFP cell fill and SEP-GluA1. Bleaching (t=0 min) and fluorescence recovery are shown (t= 5-25min). Scale bar 50 μm (top) and 10 μm (bottom). (C) Fluorescence recovery is reduced in duplication neurons indicating impaired GluA1 insertion (repeated measures two-way ANOVA with Šídák post-hoc test, p = 0.0153). Data are displayed as mean ± s.e.m. *p < 0.05. Abbreviations: WT, 16p11.2 +/+ ; Dup, 16p11.2 dup/+ .

    Article Snippet: A piece of the gel including the somatosensory cortex was cut and transferred into a FluoroDish FD35 (World Precision instrument) and images were collected on a Nikon AXR point scanning confocal fluorescence microscope using a Nikon CFI Apo LWD Lambda S 40XC WI objective and GaAsP point detectors.

    Techniques: Imaging, Activity Assay, Transfection, Fluorescence, Microscopy, Expressing