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inverted microscope eclipse ts2  (Nikon)


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    Structured Review

    Nikon inverted microscope eclipse ts2
    Inverted Microscope Eclipse Ts2, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 14726 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+ts2+fl+microscope/Inverted+Microscopes/ppr0955708-75-6-10
    Average 99 stars, based on 14726 article reviews
    inverted microscope eclipse ts2 - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Fluorescence:

    Article Title: Synergistic mitochondrial homeostasis regulation and cholinergic circuits reconstruction via a one-step synthesized multifunctional hydrogel facilitates spinal cord injury repair
    Article Snippet: .. Fluorescence images were captured using a Nikon inverted fluorescence microscope, and the MitoSOX Red fluorescence intensity was quantitatively analyzed using NIS-Elements AR software. ..

    Article Title: Distribution and functional significance of rodent cerebellar glycogen
    Article Snippet: .. Epifluorescence images of coronal or sagittal sections were acquired using an inverted fluorescence microscope (Nikon ECLIPSE Ni-E, Mono-Camera Nikon DS-Fi3) controlled by proprietary software (NIS-Elements Imaging AR 4.60.00). .. Confocal images were acquired with a Nikon Eclipse Ti2 microscope (NIS-Elements AR 4.50.00) with a Plan Apo x60/1.40 numerical aperture (NA) oil-immersion objective at a Z step of 1 μm.

    Article Title: Integrated fabrication of a shape-adaptable, antioxidative composite stent for effective closure and biological repair of enteroatmospheric fistula
    Article Snippet: .. An inverted fluorescence microscope (Nikon, TiS, Japan) was applied to capture images. ..

    Article Title: Synergistic mitochondrial homeostasis regulation and cholinergic circuits reconstruction via a one-step synthesized multifunctional hydrogel facilitates spinal cord injury repair
    Article Snippet: .. For ROS detection, 10 μM DCFH-DA or DHE working solution was added, followed by incubation at 37 °C in the dark for 30 min. For mtROS detection, PC12 cells was incubated with 5 μM MitoSox Red working solution under the same conditions in the dark for 15 min. Fluorescence images were acquired using a Nikon inverted fluorescence microscope (Nikon, Japan). .. All images were quantitatively analyzed using NIS-Elements AR software (Version 5.11, Nikon) to ensure the accuracy and reproducibility of experimental results.

    Article Title: Synergistic mitochondrial homeostasis regulation and cholinergic circuits reconstruction via a one-step synthesized multifunctional hydrogel facilitates spinal cord injury repair
    Article Snippet: The next day, after three PBS washes, fluorescently labeled secondary antibodies (Alexa Fluor 488 or 594, 1:500; Abcam) were added and incubated in the dark at room temperature for 1 h. Unbound secondary antibodies were washed away, and cell nuclei were stained with DAPI for 5 min. .. Finally, the cells were washed three times with PBS, mounted with anti-fluorescence quenching medium, and fluorescence images were acquired using a Nikon inverted fluorescence microscope (Nikon, Japan). .. All images were quantitatively analyzed using NIS-Elements AR software (Version 5.11, Nikon) to ensure data accuracy and reproducibility.

    Microscopy:

    Article Title: Synergistic mitochondrial homeostasis regulation and cholinergic circuits reconstruction via a one-step synthesized multifunctional hydrogel facilitates spinal cord injury repair
    Article Snippet: .. Fluorescence images were captured using a Nikon inverted fluorescence microscope, and the MitoSOX Red fluorescence intensity was quantitatively analyzed using NIS-Elements AR software. ..

    Article Title: Structural Color Inkjet Printing With Mie-Resonant Silicon Nanoparticles.
    Article Snippet: Elemental mapping was performed using scanning transmission electron microscopy (STEM; JEM-2100F, JEOL) equipped with an energy-dispersive X-ray spectrometer (EDX; JED-2300, JEOL). .. Reflectance and transmittance spectra were measured via microspectroscopy using an inverted optical microscope (Ti-U, Nikon). ..

    Article Title: Distribution and functional significance of rodent cerebellar glycogen
    Article Snippet: .. Epifluorescence images of coronal or sagittal sections were acquired using an inverted fluorescence microscope (Nikon ECLIPSE Ni-E, Mono-Camera Nikon DS-Fi3) controlled by proprietary software (NIS-Elements Imaging AR 4.60.00). .. Confocal images were acquired with a Nikon Eclipse Ti2 microscope (NIS-Elements AR 4.50.00) with a Plan Apo x60/1.40 numerical aperture (NA) oil-immersion objective at a Z step of 1 μm.

    Article Title: Integrated fabrication of a shape-adaptable, antioxidative composite stent for effective closure and biological repair of enteroatmospheric fistula
    Article Snippet: .. An inverted fluorescence microscope (Nikon, TiS, Japan) was applied to capture images. ..

    Article Title: Synergistic mitochondrial homeostasis regulation and cholinergic circuits reconstruction via a one-step synthesized multifunctional hydrogel facilitates spinal cord injury repair
    Article Snippet: .. For ROS detection, 10 μM DCFH-DA or DHE working solution was added, followed by incubation at 37 °C in the dark for 30 min. For mtROS detection, PC12 cells was incubated with 5 μM MitoSox Red working solution under the same conditions in the dark for 15 min. Fluorescence images were acquired using a Nikon inverted fluorescence microscope (Nikon, Japan). .. All images were quantitatively analyzed using NIS-Elements AR software (Version 5.11, Nikon) to ensure the accuracy and reproducibility of experimental results.

    Article Title: Synergistic mitochondrial homeostasis regulation and cholinergic circuits reconstruction via a one-step synthesized multifunctional hydrogel facilitates spinal cord injury repair
    Article Snippet: The next day, after three PBS washes, fluorescently labeled secondary antibodies (Alexa Fluor 488 or 594, 1:500; Abcam) were added and incubated in the dark at room temperature for 1 h. Unbound secondary antibodies were washed away, and cell nuclei were stained with DAPI for 5 min. .. Finally, the cells were washed three times with PBS, mounted with anti-fluorescence quenching medium, and fluorescence images were acquired using a Nikon inverted fluorescence microscope (Nikon, Japan). .. All images were quantitatively analyzed using NIS-Elements AR software (Version 5.11, Nikon) to ensure data accuracy and reproducibility.

    Software:

    Article Title: Synergistic mitochondrial homeostasis regulation and cholinergic circuits reconstruction via a one-step synthesized multifunctional hydrogel facilitates spinal cord injury repair
    Article Snippet: .. Fluorescence images were captured using a Nikon inverted fluorescence microscope, and the MitoSOX Red fluorescence intensity was quantitatively analyzed using NIS-Elements AR software. ..

    Article Title: Distribution and functional significance of rodent cerebellar glycogen
    Article Snippet: .. Epifluorescence images of coronal or sagittal sections were acquired using an inverted fluorescence microscope (Nikon ECLIPSE Ni-E, Mono-Camera Nikon DS-Fi3) controlled by proprietary software (NIS-Elements Imaging AR 4.60.00). .. Confocal images were acquired with a Nikon Eclipse Ti2 microscope (NIS-Elements AR 4.50.00) with a Plan Apo x60/1.40 numerical aperture (NA) oil-immersion objective at a Z step of 1 μm.

    Incubation:

    Article Title: MS4322 is a selective protein arginine methyltransferase 5 degrader with antitumor effects in cervical cancer cells
    Article Snippet: The cell monolayer was scraped with a 10 μl pipette tip to produce a wound, washed with PBS to remove detached cells and the cells were incubated in serum-free DMEM (Gibco; Thermo Fisher Scientific, Inc.). .. Cells were incubated at 37°C for 24 h. Photographs were taken at 0 and 24 h using a Nikon inverted light microscope (Nikon Instruments). .. Wound width analysis was performed with Image-Pro Plus 6.0 software (Media Cybernetics, Inc.).

    Article Title: Synergistic mitochondrial homeostasis regulation and cholinergic circuits reconstruction via a one-step synthesized multifunctional hydrogel facilitates spinal cord injury repair
    Article Snippet: .. For ROS detection, 10 μM DCFH-DA or DHE working solution was added, followed by incubation at 37 °C in the dark for 30 min. For mtROS detection, PC12 cells was incubated with 5 μM MitoSox Red working solution under the same conditions in the dark for 15 min. Fluorescence images were acquired using a Nikon inverted fluorescence microscope (Nikon, Japan). .. All images were quantitatively analyzed using NIS-Elements AR software (Version 5.11, Nikon) to ensure the accuracy and reproducibility of experimental results.

    Light Microscopy:

    Article Title: MS4322 is a selective protein arginine methyltransferase 5 degrader with antitumor effects in cervical cancer cells
    Article Snippet: The cell monolayer was scraped with a 10 μl pipette tip to produce a wound, washed with PBS to remove detached cells and the cells were incubated in serum-free DMEM (Gibco; Thermo Fisher Scientific, Inc.). .. Cells were incubated at 37°C for 24 h. Photographs were taken at 0 and 24 h using a Nikon inverted light microscope (Nikon Instruments). .. Wound width analysis was performed with Image-Pro Plus 6.0 software (Media Cybernetics, Inc.).

    Staining:

    Article Title: Histone H3K9 lactylation activates the TXNIP/NLRP3 pathway to drive macrophage inflammation after spinal cord injury
    Article Snippet: Sections were stained with a H&E Staining Kit (Beyotime, C0105S) according to the manufacturer's instructions. .. Stained sections were imaged on a Nikon inverted microscope and analyzed using ImageJ. ..

    Inverted Microscopy:

    Article Title: Histone H3K9 lactylation activates the TXNIP/NLRP3 pathway to drive macrophage inflammation after spinal cord injury
    Article Snippet: Sections were stained with a H&E Staining Kit (Beyotime, C0105S) according to the manufacturer's instructions. .. Stained sections were imaged on a Nikon inverted microscope and analyzed using ImageJ. ..

    Imaging:

    Article Title: Distribution and functional significance of rodent cerebellar glycogen
    Article Snippet: .. Epifluorescence images of coronal or sagittal sections were acquired using an inverted fluorescence microscope (Nikon ECLIPSE Ni-E, Mono-Camera Nikon DS-Fi3) controlled by proprietary software (NIS-Elements Imaging AR 4.60.00). .. Confocal images were acquired with a Nikon Eclipse Ti2 microscope (NIS-Elements AR 4.50.00) with a Plan Apo x60/1.40 numerical aperture (NA) oil-immersion objective at a Z step of 1 μm.



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    KY-05009 impairs platelet tethering to immobilized fibrinogen. Adhesion of (A) vehicle (0.5% v/v dimethylsulfoxide [DMSO]) or (B) KY-05009 (10 μM)-treated platelets (4 × 10 7 cells/mL) to fibrinogen (100 μg/mL). F-actin was stained with Alexa Fluor 568 phalloidin (1:100 dilution). Platelets were visualized with a Nikon Eclipse <t>Ts2</t> Fl <t>microscope</t> using a 40X/0.65 objective. Representative images are shown: (C) percentage platelet coverage and (D) mean data; n = 4. Data are presented as mean ± SEM. Data analyzed by 1-way ANOVA; ∗ P < .03.
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    Nikon fluorescence microscope nikon eclipse ts2-fl
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    Image Search Results


    KY-05009 impairs platelet tethering to immobilized fibrinogen. Adhesion of (A) vehicle (0.5% v/v dimethylsulfoxide [DMSO]) or (B) KY-05009 (10 μM)-treated platelets (4 × 10 7 cells/mL) to fibrinogen (100 μg/mL). F-actin was stained with Alexa Fluor 568 phalloidin (1:100 dilution). Platelets were visualized with a Nikon Eclipse Ts2 Fl microscope using a 40X/0.65 objective. Representative images are shown: (C) percentage platelet coverage and (D) mean data; n = 4. Data are presented as mean ± SEM. Data analyzed by 1-way ANOVA; ∗ P < .03.

    Journal: Research and Practice in Thrombosis and Haemostasis

    Article Title: TRAF2 and NCK interacting kinase: a novel regulator of integrin α IIb β 3 signaling in platelets

    doi: 10.1016/j.rpth.2025.103204

    Figure Lengend Snippet: KY-05009 impairs platelet tethering to immobilized fibrinogen. Adhesion of (A) vehicle (0.5% v/v dimethylsulfoxide [DMSO]) or (B) KY-05009 (10 μM)-treated platelets (4 × 10 7 cells/mL) to fibrinogen (100 μg/mL). F-actin was stained with Alexa Fluor 568 phalloidin (1:100 dilution). Platelets were visualized with a Nikon Eclipse Ts2 Fl microscope using a 40X/0.65 objective. Representative images are shown: (C) percentage platelet coverage and (D) mean data; n = 4. Data are presented as mean ± SEM. Data analyzed by 1-way ANOVA; ∗ P < .03.

    Article Snippet: Representative images were taken using a Nikon Eclipse Ts2 Fl microscope with a 40X/0.65 objective.

    Techniques: Staining, Microscopy

    KY-05009 treatment attenuates thrombus formation under arterial shear stress. DIOC6 labeled whole blood was treated with (A) vehicle (DMSO, 1% v/v), (B) KY-05009 (10 μM), (C) KY-05009 (50 μM), or (D) KY-05009 (100 μM) and perfused over collagen coated (100μg/mL) Vena8 Fluoro+ Biochips using a Cellix perfusion system at arterial sheer stress (20 dynes/cm 2 ) for 10 minutes. Thrombus formation was determined by monitoring the change in fluorescence intensity observed over recorded intervals. Representative images were taken using a Nikon Eclipse Ts2 Fl microscope with a 40X/0.65 objective. The fluorescence intensity of the formed thrombi were normalized to the maximum fluorescence intensity value of the vehicle after 10 minutes and expressed as a percentage; n = 6. Decimated averages at each time point are presented ± SEM. (E) Annexin V binding to platelets treated with vehicle (DMSO, 1% v/v) or KY-005009 (10-100 μM). Platelets were gated and 10 000 events were recorded. Mean ± SEM of raw median fluorescence intensity data are presented; n = 3. Thrombus formation data analyzed by 2-way ANOVA; flow cytometry data analyzed by 1-way ANOVA; ∗ P < .03.

    Journal: Research and Practice in Thrombosis and Haemostasis

    Article Title: TRAF2 and NCK interacting kinase: a novel regulator of integrin α IIb β 3 signaling in platelets

    doi: 10.1016/j.rpth.2025.103204

    Figure Lengend Snippet: KY-05009 treatment attenuates thrombus formation under arterial shear stress. DIOC6 labeled whole blood was treated with (A) vehicle (DMSO, 1% v/v), (B) KY-05009 (10 μM), (C) KY-05009 (50 μM), or (D) KY-05009 (100 μM) and perfused over collagen coated (100μg/mL) Vena8 Fluoro+ Biochips using a Cellix perfusion system at arterial sheer stress (20 dynes/cm 2 ) for 10 minutes. Thrombus formation was determined by monitoring the change in fluorescence intensity observed over recorded intervals. Representative images were taken using a Nikon Eclipse Ts2 Fl microscope with a 40X/0.65 objective. The fluorescence intensity of the formed thrombi were normalized to the maximum fluorescence intensity value of the vehicle after 10 minutes and expressed as a percentage; n = 6. Decimated averages at each time point are presented ± SEM. (E) Annexin V binding to platelets treated with vehicle (DMSO, 1% v/v) or KY-005009 (10-100 μM). Platelets were gated and 10 000 events were recorded. Mean ± SEM of raw median fluorescence intensity data are presented; n = 3. Thrombus formation data analyzed by 2-way ANOVA; flow cytometry data analyzed by 1-way ANOVA; ∗ P < .03.

    Article Snippet: Representative images were taken using a Nikon Eclipse Ts2 Fl microscope with a 40X/0.65 objective.

    Techniques: Shear, Labeling, Fluorescence, Microscopy, Binding Assay, Flow Cytometry