inverted microscope eclipse ts2 (Nikon)
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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
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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 Article Title: Distribution and functional significance of rodent cerebellar glycogen Article Snippet: .. Epifluorescence images of coronal or sagittal sections were acquired using an Article Title: Integrated fabrication of a shape-adaptable, antioxidative composite stent for effective closure and biological repair of enteroatmospheric fistula Article Snippet: .. An 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 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 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 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 Article Title: Distribution and functional significance of rodent cerebellar glycogen Article Snippet: .. Epifluorescence images of coronal or sagittal sections were acquired using an Article Title: Integrated fabrication of a shape-adaptable, antioxidative composite stent for effective closure and biological repair of enteroatmospheric fistula Article Snippet: .. An 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 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 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 Article Title: Distribution and functional significance of rodent cerebellar glycogen Article Snippet: .. Epifluorescence images of coronal or sagittal sections were acquired using an 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 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 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 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 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 Imaging:Article Title: Distribution and functional significance of rodent cerebellar glycogen Article Snippet: .. Epifluorescence images of coronal or sagittal sections were acquired using an |
![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.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_6069/pmc12616069/pmc12616069__gr2.jpg)