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eclipse ts2 fl inverted microscopes  (Nikon)


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    Structured Review

    Nikon eclipse ts2 fl inverted microscopes
    Eclipse Ts2 Fl Inverted Microscopes, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 14758 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+ts2-fl/Inverted+Microscopes/10__1038_slash_s41598___026___72920___1-80-16-15
    Average 99 stars, based on 14758 article reviews
    eclipse ts2 fl inverted microscopes - by Bioz Stars, 2026-11
    99/100 stars

    Images

    Related Articles

    Fluorescence:

    Article Title: Tensile Property of iPP Based Composites Embedding “Plant Cell Wall”-Mimicked Frameworks of Ultratrace Amphiphilic Cellulose Nanofibrils Derived from Various Raw Materials
    Article Snippet: Fluorescent microscopic observation was carried out by ECLIPSE Ts2-FL (Nikon Solutions Co., Ltd., Tokyo, Japan) under DAPI filter at under excitation wavelengths and emission wavelength of 361-389 nm and 430-490 nm, respectively.

    Article Title: miR-4284 Functions as a Tumor Suppressor in Renal Cell Carcinoma Cells by Targeting Glutamate Decarboxylase 1
    Article Snippet: The cells were washed once with PBS, fixed with methanol for 5 min, stained with 0.05% crystal violet solution (Sigma-Aldrich, Burlington, MA, USA) in 10% ethanol for 10 min, rinsed with distilled water, and dried after incubation for 72 h. The stained cells were then captured using Nikon Eclipse Ts2-FL Diascopic and Epi-fluorescence illumination model and counted.

    Article Title: Network pharmacology- and cell-based assessments identify the FAK/Src pathway as a molecular target for the antimetastatic effect of momordin Ic against cholangiocarcinoma
    Article Snippet: Subsequently, the cells were mounted with VECTASHIELD® PLUS Antifade Mounting Medium with DAPI (Vector Laboratories, CA, USA, H-1200-10), visualized and photographed under an upright fluorescence microscope (Nikon Eclipse TS2-FL, Nikon Instruments Inc., Japan).

    Article Title: Caffeine reduces viability, induces apoptosis, inhibits migration and modulates the CD39/CD73 axis in metastatic cutaneous melanoma cells
    Article Snippet: For fluorescence assays, a fluorescence microscope was used (Nikon® Eclipse TS2-FL).

    Article Title: Diverse clonal fates emerge upon drug treatment of homogeneous cancer cells
    Article Snippet: For bright-field imaging of resistant colonies, we used a Nikon Eclipse TS2-FL with an Imagingsource DFK 33UX252 camera and 4× Plan-Fluor 4×/0.13 (Nikon MRH20041) objective.

    Article Title: miR-4284 Functions as a Tumor Suppressor in Renal Cell Carcinoma Cells by Targeting Glutamate Decarboxylase 1.
    Article Snippet: The cells were washed once with PBS, fixed with methanol for 5 min, stained with 0.05% crystal violet solution (Sigma-Aldrich, Burlington, MA, USA) in 10% ethanol for 10 min, rinsed with distilled water, and dried after incubation for 72 h. The stained cells were then captured using Nikon Eclipse Ts2-FL Diascopic and Epi-fluorescence illumination model and counted.

    Article Title: Formation of Zwitterionic and Self-Healable Hydrogels via Amino-yne Click Chemistry for Development of Cellular Scaffold and Tumor Spheroid Phantom for MRI.
    Article Snippet: The LIVE/DEAD Viability Kit was used to observe the growth of cells in the hydrogel under a fluorescent microscope (Nikon Eclipse, Ts2-FL, Japan).

    Article Title: Construction of a recombinant vaccine expressing Nipah virus glycoprotein using the replicative and highly attenuated vaccinia virus strain LC16m8
    Article Snippet: After 2–3 days, plaques that were double-positive for mCherry and EGFP fluorescence signals were identified using a fluorescence microscope Eclipse Ts2-FL (Nikon, Tokyo, Japan).

    Microscopy:

    Article Title: Tensile Property of iPP Based Composites Embedding “Plant Cell Wall”-Mimicked Frameworks of Ultratrace Amphiphilic Cellulose Nanofibrils Derived from Various Raw Materials
    Article Snippet: Fluorescent microscopic observation was carried out by ECLIPSE Ts2-FL (Nikon Solutions Co., Ltd., Tokyo, Japan) under DAPI filter at under excitation wavelengths and emission wavelength of 361-389 nm and 430-490 nm, respectively.

    Article Title: miR-4284 Functions as a Tumor Suppressor in Renal Cell Carcinoma Cells by Targeting Glutamate Decarboxylase 1
    Article Snippet: The cells were washed once with PBS, fixed with methanol for 5 min, stained with 0.05% crystal violet solution (Sigma-Aldrich, Burlington, MA, USA) in 10% ethanol for 10 min, rinsed with distilled water, and dried after incubation for 72 h. The stained cells were then captured using Nikon Eclipse Ts2-FL Diascopic and Epi-fluorescence illumination model and counted.

    Article Title: Network pharmacology- and cell-based assessments identify the FAK/Src pathway as a molecular target for the antimetastatic effect of momordin Ic against cholangiocarcinoma
    Article Snippet: Subsequently, the cells were mounted with VECTASHIELD® PLUS Antifade Mounting Medium with DAPI (Vector Laboratories, CA, USA, H-1200-10), visualized and photographed under an upright fluorescence microscope (Nikon Eclipse TS2-FL, Nikon Instruments Inc., Japan).

    Article Title: Caffeine reduces viability, induces apoptosis, inhibits migration and modulates the CD39/CD73 axis in metastatic cutaneous melanoma cells
    Article Snippet: For fluorescence assays, a fluorescence microscope was used (Nikon® Eclipse TS2-FL).

    Article Title: Diverse clonal fates emerge upon drug treatment of homogeneous cancer cells
    Article Snippet: For bright-field imaging of resistant colonies, we used a Nikon Eclipse TS2-FL with an Imagingsource DFK 33UX252 camera and 4× Plan-Fluor 4×/0.13 (Nikon MRH20041) objective.

    Article Title: miR-4284 Functions as a Tumor Suppressor in Renal Cell Carcinoma Cells by Targeting Glutamate Decarboxylase 1.
    Article Snippet: The cells were washed once with PBS, fixed with methanol for 5 min, stained with 0.05% crystal violet solution (Sigma-Aldrich, Burlington, MA, USA) in 10% ethanol for 10 min, rinsed with distilled water, and dried after incubation for 72 h. The stained cells were then captured using Nikon Eclipse Ts2-FL Diascopic and Epi-fluorescence illumination model and counted.

    Article Title: Formation of Zwitterionic and Self-Healable Hydrogels via Amino-yne Click Chemistry for Development of Cellular Scaffold and Tumor Spheroid Phantom for MRI.
    Article Snippet: The LIVE/DEAD Viability Kit was used to observe the growth of cells in the hydrogel under a fluorescent microscope (Nikon Eclipse, Ts2-FL, Japan).

    Article Title: Construction of a recombinant vaccine expressing Nipah virus glycoprotein using the replicative and highly attenuated vaccinia virus strain LC16m8
    Article Snippet: After 2–3 days, plaques that were double-positive for mCherry and EGFP fluorescence signals were identified using a fluorescence microscope Eclipse Ts2-FL (Nikon, Tokyo, Japan).

    Staining:

    Article Title: Tensile Property of iPP Based Composites Embedding “Plant Cell Wall”-Mimicked Frameworks of Ultratrace Amphiphilic Cellulose Nanofibrils Derived from Various Raw Materials
    Article Snippet: Fluorescent microscopic observation was carried out by ECLIPSE Ts2-FL (Nikon Solutions Co., Ltd., Tokyo, Japan) under DAPI filter at under excitation wavelengths and emission wavelength of 361-389 nm and 430-490 nm, respectively.

    Article Title: miR-4284 Functions as a Tumor Suppressor in Renal Cell Carcinoma Cells by Targeting Glutamate Decarboxylase 1
    Article Snippet: The cells were washed once with PBS, fixed with methanol for 5 min, stained with 0.05% crystal violet solution (Sigma-Aldrich, Burlington, MA, USA) in 10% ethanol for 10 min, rinsed with distilled water, and dried after incubation for 72 h. The stained cells were then captured using Nikon Eclipse Ts2-FL Diascopic and Epi-fluorescence illumination model and counted.

    Article Title: Network pharmacology- and cell-based assessments identify the FAK/Src pathway as a molecular target for the antimetastatic effect of momordin Ic against cholangiocarcinoma
    Article Snippet: Subsequently, the cells were mounted with VECTASHIELD® PLUS Antifade Mounting Medium with DAPI (Vector Laboratories, CA, USA, H-1200-10), visualized and photographed under an upright fluorescence microscope (Nikon Eclipse TS2-FL, Nikon Instruments Inc., Japan).

    Article Title: Caffeine reduces viability, induces apoptosis, inhibits migration and modulates the CD39/CD73 axis in metastatic cutaneous melanoma cells
    Article Snippet: For fluorescence assays, a fluorescence microscope was used (Nikon® Eclipse TS2-FL).

    Article Title: Diverse clonal fates emerge upon drug treatment of homogeneous cancer cells
    Article Snippet: For bright-field imaging of resistant colonies, we used a Nikon Eclipse TS2-FL with an Imagingsource DFK 33UX252 camera and 4× Plan-Fluor 4×/0.13 (Nikon MRH20041) objective.

    Article Title: miR-4284 Functions as a Tumor Suppressor in Renal Cell Carcinoma Cells by Targeting Glutamate Decarboxylase 1.
    Article Snippet: The cells were washed once with PBS, fixed with methanol for 5 min, stained with 0.05% crystal violet solution (Sigma-Aldrich, Burlington, MA, USA) in 10% ethanol for 10 min, rinsed with distilled water, and dried after incubation for 72 h. The stained cells were then captured using Nikon Eclipse Ts2-FL Diascopic and Epi-fluorescence illumination model and counted.

    Article Title: Formation of Zwitterionic and Self-Healable Hydrogels via Amino-yne Click Chemistry for Development of Cellular Scaffold and Tumor Spheroid Phantom for MRI.
    Article Snippet: The LIVE/DEAD Viability Kit was used to observe the growth of cells in the hydrogel under a fluorescent microscope (Nikon Eclipse, Ts2-FL, Japan).

    Article Title: Construction of a recombinant vaccine expressing Nipah virus glycoprotein using the replicative and highly attenuated vaccinia virus strain LC16m8
    Article Snippet: After 2–3 days, plaques that were double-positive for mCherry and EGFP fluorescence signals were identified using a fluorescence microscope Eclipse Ts2-FL (Nikon, Tokyo, Japan).

    Incubation:

    Article Title: Tensile Property of iPP Based Composites Embedding “Plant Cell Wall”-Mimicked Frameworks of Ultratrace Amphiphilic Cellulose Nanofibrils Derived from Various Raw Materials
    Article Snippet: Fluorescent microscopic observation was carried out by ECLIPSE Ts2-FL (Nikon Solutions Co., Ltd., Tokyo, Japan) under DAPI filter at under excitation wavelengths and emission wavelength of 361-389 nm and 430-490 nm, respectively.

    Article Title: miR-4284 Functions as a Tumor Suppressor in Renal Cell Carcinoma Cells by Targeting Glutamate Decarboxylase 1
    Article Snippet: The cells were washed once with PBS, fixed with methanol for 5 min, stained with 0.05% crystal violet solution (Sigma-Aldrich, Burlington, MA, USA) in 10% ethanol for 10 min, rinsed with distilled water, and dried after incubation for 72 h. The stained cells were then captured using Nikon Eclipse Ts2-FL Diascopic and Epi-fluorescence illumination model and counted.

    Article Title: Network pharmacology- and cell-based assessments identify the FAK/Src pathway as a molecular target for the antimetastatic effect of momordin Ic against cholangiocarcinoma
    Article Snippet: Subsequently, the cells were mounted with VECTASHIELD® PLUS Antifade Mounting Medium with DAPI (Vector Laboratories, CA, USA, H-1200-10), visualized and photographed under an upright fluorescence microscope (Nikon Eclipse TS2-FL, Nikon Instruments Inc., Japan).

    Article Title: Caffeine reduces viability, induces apoptosis, inhibits migration and modulates the CD39/CD73 axis in metastatic cutaneous melanoma cells
    Article Snippet: For fluorescence assays, a fluorescence microscope was used (Nikon® Eclipse TS2-FL).

    Article Title: Diverse clonal fates emerge upon drug treatment of homogeneous cancer cells
    Article Snippet: For bright-field imaging of resistant colonies, we used a Nikon Eclipse TS2-FL with an Imagingsource DFK 33UX252 camera and 4× Plan-Fluor 4×/0.13 (Nikon MRH20041) objective.

    Article Title: miR-4284 Functions as a Tumor Suppressor in Renal Cell Carcinoma Cells by Targeting Glutamate Decarboxylase 1.
    Article Snippet: The cells were washed once with PBS, fixed with methanol for 5 min, stained with 0.05% crystal violet solution (Sigma-Aldrich, Burlington, MA, USA) in 10% ethanol for 10 min, rinsed with distilled water, and dried after incubation for 72 h. The stained cells were then captured using Nikon Eclipse Ts2-FL Diascopic and Epi-fluorescence illumination model and counted.

    Article Title: Formation of Zwitterionic and Self-Healable Hydrogels via Amino-yne Click Chemistry for Development of Cellular Scaffold and Tumor Spheroid Phantom for MRI.
    Article Snippet: The LIVE/DEAD Viability Kit was used to observe the growth of cells in the hydrogel under a fluorescent microscope (Nikon Eclipse, Ts2-FL, Japan).

    Article Title: Construction of a recombinant vaccine expressing Nipah virus glycoprotein using the replicative and highly attenuated vaccinia virus strain LC16m8
    Article Snippet: After 2–3 days, plaques that were double-positive for mCherry and EGFP fluorescence signals were identified using a fluorescence microscope Eclipse Ts2-FL (Nikon, Tokyo, Japan).



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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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    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