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dedicated imagej plugin  (Nikon)


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    Structured Review

    Nikon dedicated imagej plugin
    Dedicated Imagej Plugin, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1614 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/imagej+plugins/ECLIPSE+Ts2R/pm41780697-118-15-8
    Average 99 stars, based on 1614 article reviews
    dedicated imagej plugin - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Microscopy:

    Article Title: Cellular models of and therapies for ocular diseases
    Article Snippet: Real-time PCR method was performed using Maxima SYBR Green/ROX qPCR Master Mix (Fisher Scientific) with StepOne Real-time PCR System (Invitrogen) to quantify gene expression levels (38 cycles). .. Then after washing with PBS (−), cellular fluorescent levels were observed and photos were taken by inverted fluorescent microscope (Nikon Eclipse Ts2R) at 20 times magnification. ..

    Article Title: Multi-omics analysis reveals RBPJ-mediated regulation of EGF/ACTN2 / MYPN / COL21A1 in fibroblast during oviduct functional remodeling of duck
    Article Snippet: Cells were then incubated with AF594-labeled Rabbit Anti-Mouse IgG (1:10000, K1031R-AF594, Solarbio, China) and Hochest 33342 (1:10000, B2261, Merck, Germany) for 1 h at RT in the dark. .. Subsequently, cells were washed three times with 1 × TBST for 5 min each, and fluorescence images were acquired using a Nikon ECLIPSE Ts2R-FL fluorescence microscope (Nikon, Japan). ..

    Article Title: Multi-omics analysis reveals RBPJ-mediated regulation of EGF/ACTN2 / MYPN / COL21A1 in fibroblast during oviduct functional remodeling of duck
    Article Snippet: Cell nuclei were stained with Hoechst 33342 (1:10000 dilution, 14533, Merck, Germany) for 10 min at RT to visualize total cells. .. Fluorescence images were captured using a Nikon ECLIPSE Ts2R-FL fluorescence microscope (Nikon, Japan). ..

    other:

    Article Title: Boosting ribosomal translation via ionizable lipid-hydrogel microplexes for localized mRNA therapy
    Article Snippet: We chose mCherry mRNA as a model, prepared mRNA-iLMPs, coincubated them with MC3T3-E1 cells, and observed the transfection efficiency by fluorescence microscopy (Nikon ECLIPSE Ts2R, Japan).

    Fluorescence:

    Article Title: Multi-omics analysis reveals RBPJ-mediated regulation of EGF/ACTN2 / MYPN / COL21A1 in fibroblast during oviduct functional remodeling of duck
    Article Snippet: Cells were then incubated with AF594-labeled Rabbit Anti-Mouse IgG (1:10000, K1031R-AF594, Solarbio, China) and Hochest 33342 (1:10000, B2261, Merck, Germany) for 1 h at RT in the dark. .. Subsequently, cells were washed three times with 1 × TBST for 5 min each, and fluorescence images were acquired using a Nikon ECLIPSE Ts2R-FL fluorescence microscope (Nikon, Japan). ..

    Article Title: Multi-omics analysis reveals RBPJ-mediated regulation of EGF/ACTN2 / MYPN / COL21A1 in fibroblast during oviduct functional remodeling of duck
    Article Snippet: Cell nuclei were stained with Hoechst 33342 (1:10000 dilution, 14533, Merck, Germany) for 10 min at RT to visualize total cells. .. Fluorescence images were captured using a Nikon ECLIPSE Ts2R-FL fluorescence microscope (Nikon, Japan). ..

    Imaging:

    Article Title: Salinomycin as a death switch: how gastric cancer cells choose their demise.
    Article Snippet: .. Spheroids growth and radius were monitored over 14 days, and images were captured at days 3, 7, 10, and 14 through the Eclipse Ts2R imaging system (Nikon Europe, Amstelveen, The Netherlands) using the included software. ..

    Software:

    Article Title: Salinomycin as a death switch: how gastric cancer cells choose their demise.
    Article Snippet: .. Spheroids growth and radius were monitored over 14 days, and images were captured at days 3, 7, 10, and 14 through the Eclipse Ts2R imaging system (Nikon Europe, Amstelveen, The Netherlands) using the included software. ..



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    Quantification of wound assay, Golgi appearance and microtubule distribution in patient-derived fibroblasts compared to control . (a) Representative images of sub-confluent fibroblast cells derived from either the index individual in Family 1 (IV:1) or control cell lines at 0 h of wound-induced cell migration assay. Scale bar: 1000 μm. (b) Wound closure was followed serially for 29 h during which a significant difference in cell migration was observed between the two cell lines. Scale bar: 1000 μm. (c) Percent wound closure was evaluated up to 29 h. (d) The remaining area of the wound was measured in μm 2 . The percent wound closure and area of the wound were measured using the <t>ImageJ</t> <t>plugin</t> Wound healing size tool image tool analysis ( https://github.com/AlejandraArnedo/Wound-healing-size-tool/wiki ). Data from 50 cells were collected and analysed. (e) Control cells showing perinuclear compact and polarized Golgi apparatus that are directed toward the migrating wound edge. (f) IV:1-derived fibroblast cells depicting a dispersed and non-polarized (oriented) Golgi apparatus towards the migrating/wound edge. (g) A representative image of normally polarized and parallel orientated microtubules in control cells. (h) A representative image of individual IV:1-derived fibroblast cells showing an un-polarized chaotic microtubule distribution; microtubules labelled with α-tubulin (green) and the centrosome is labelled with Pericentrin (orange) antibodies. (i) The total area of Golgi from 100 cells was measured using the ImageJ software. Error bars represent stdev. (j) The directional orientation of Golgi from 100 cells was assessed and presented as percent mean polarization with error bars representing stdev of 3 replicates. (k) The direction of orientation (paralellness) of microtubules was measured using the <t>LPX</t> ImageJ plugin ( https://lpixel.net/services/research/lpixel-imagej-plugins/ ) ; and data presented as mean and stdev of images of 100 cells. Data from 50 cells were collected and analysed and p-value was calculated based on Welch's t-test for (c, d, i, j and k). The red squares represent datapoints collected from control sample, the green circles represent datapoints collected from the patient sample (IV:1). The horizontal line represents the mean.
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    Image Search Results


    Quantification of wound assay, Golgi appearance and microtubule distribution in patient-derived fibroblasts compared to control . (a) Representative images of sub-confluent fibroblast cells derived from either the index individual in Family 1 (IV:1) or control cell lines at 0 h of wound-induced cell migration assay. Scale bar: 1000 μm. (b) Wound closure was followed serially for 29 h during which a significant difference in cell migration was observed between the two cell lines. Scale bar: 1000 μm. (c) Percent wound closure was evaluated up to 29 h. (d) The remaining area of the wound was measured in μm 2 . The percent wound closure and area of the wound were measured using the ImageJ plugin Wound healing size tool image tool analysis ( https://github.com/AlejandraArnedo/Wound-healing-size-tool/wiki ). Data from 50 cells were collected and analysed. (e) Control cells showing perinuclear compact and polarized Golgi apparatus that are directed toward the migrating wound edge. (f) IV:1-derived fibroblast cells depicting a dispersed and non-polarized (oriented) Golgi apparatus towards the migrating/wound edge. (g) A representative image of normally polarized and parallel orientated microtubules in control cells. (h) A representative image of individual IV:1-derived fibroblast cells showing an un-polarized chaotic microtubule distribution; microtubules labelled with α-tubulin (green) and the centrosome is labelled with Pericentrin (orange) antibodies. (i) The total area of Golgi from 100 cells was measured using the ImageJ software. Error bars represent stdev. (j) The directional orientation of Golgi from 100 cells was assessed and presented as percent mean polarization with error bars representing stdev of 3 replicates. (k) The direction of orientation (paralellness) of microtubules was measured using the LPX ImageJ plugin ( https://lpixel.net/services/research/lpixel-imagej-plugins/ ) ; and data presented as mean and stdev of images of 100 cells. Data from 50 cells were collected and analysed and p-value was calculated based on Welch's t-test for (c, d, i, j and k). The red squares represent datapoints collected from control sample, the green circles represent datapoints collected from the patient sample (IV:1). The horizontal line represents the mean.

    Journal: eBioMedicine

    Article Title: SLK is mutated in individuals with a neurodevelopmental disorder

    doi: 10.1016/j.ebiom.2025.105725

    Figure Lengend Snippet: Quantification of wound assay, Golgi appearance and microtubule distribution in patient-derived fibroblasts compared to control . (a) Representative images of sub-confluent fibroblast cells derived from either the index individual in Family 1 (IV:1) or control cell lines at 0 h of wound-induced cell migration assay. Scale bar: 1000 μm. (b) Wound closure was followed serially for 29 h during which a significant difference in cell migration was observed between the two cell lines. Scale bar: 1000 μm. (c) Percent wound closure was evaluated up to 29 h. (d) The remaining area of the wound was measured in μm 2 . The percent wound closure and area of the wound were measured using the ImageJ plugin Wound healing size tool image tool analysis ( https://github.com/AlejandraArnedo/Wound-healing-size-tool/wiki ). Data from 50 cells were collected and analysed. (e) Control cells showing perinuclear compact and polarized Golgi apparatus that are directed toward the migrating wound edge. (f) IV:1-derived fibroblast cells depicting a dispersed and non-polarized (oriented) Golgi apparatus towards the migrating/wound edge. (g) A representative image of normally polarized and parallel orientated microtubules in control cells. (h) A representative image of individual IV:1-derived fibroblast cells showing an un-polarized chaotic microtubule distribution; microtubules labelled with α-tubulin (green) and the centrosome is labelled with Pericentrin (orange) antibodies. (i) The total area of Golgi from 100 cells was measured using the ImageJ software. Error bars represent stdev. (j) The directional orientation of Golgi from 100 cells was assessed and presented as percent mean polarization with error bars representing stdev of 3 replicates. (k) The direction of orientation (paralellness) of microtubules was measured using the LPX ImageJ plugin ( https://lpixel.net/services/research/lpixel-imagej-plugins/ ) ; and data presented as mean and stdev of images of 100 cells. Data from 50 cells were collected and analysed and p-value was calculated based on Welch's t-test for (c, d, i, j and k). The red squares represent datapoints collected from control sample, the green circles represent datapoints collected from the patient sample (IV:1). The horizontal line represents the mean.

    Article Snippet: Error bars represent stdev. (j) The directional orientation of Golgi from 100 cells was assessed and presented as percent mean polarization with error bars representing stdev of 3 replicates. (k) The direction of orientation (paralellness) of microtubules was measured using the LPX ImageJ plugin ( https://lpixel.net/services/research/lpixel-imagej-plugins/ ) ; and data presented as mean and stdev of images of 100 cells.

    Techniques: Derivative Assay, Control, Cell Migration Assay, Migration, Software