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nikon eclipse ti2 microscope  (Nikon)


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    Structured Review

    Nikon nikon eclipse ti2 microscope
    Nikon Eclipse Ti2 Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 11824 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+microscope+nikon/ECLIPSE+Ti2/pmc12989073-261-5-5
    Average 99 stars, based on 11824 article reviews
    nikon eclipse ti2 microscope - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Microscopy:

    Article Title: One step generation of single-core double emulsions from polymer-osmose-induced aqueous phase separation in polar oil droplets.
    Article Snippet: Water-in-oil-in-water emulsions (W/O/W) are aqueous droplet(s) embedded within oil droplets dispersed in a continuous water phase.. They are attracting interest due to their possible applications from cosmetic to food science since both hydrosoluble and liposoluble cargos can be encapsulated within.. They are generally prepared using a one-step or a two-step method, phase inversion and also via spontaneous emulsification.

    Article Title: Compressive stress inhibits proliferation in tumor spheroids through a volume limitation.
    Article Snippet: .. Fluorescent images are recorded on an Eclipse microscope (Nikon, Melville, NY), with a Luca S camera (ANDOR Technology, Belfast, UK). .. Image analysis are performed with a home-made software employing MATLAB (The MathWorks, Natick, MA).

    Article Title: The endothelial dysfunction blocker CU06-1004 ameliorates choline-deficient L-amino acid diet-induced non-alcoholic steatohepatitis in mice
    Article Snippet: For immunohistochemistry, paraffin-embedded sections were stained with antibodies against F4/80 (1:60; AbD Serotec, Oxford, UK, #MCA497GA), α-smooth muscle actin (α-SMA, 1:300, Abcam, #ab7817), ICAM-1 (1:200; Santa Cruz, CA, USA, #sc8439), and CD31 (1:200, R&D System, MN, USA, #AF3628). .. Images were using an eclipse microscope (Nikon, Tokyo, Japan), and the Sirius Red, F4/80, α-SMA, ICAM-1, and CD31-positive areas were quantified using Image J. ..

    Article Title: piragua encodes a zinc finger protein required for development in Drosophila.
    Article Snippet: We mounted embryos in Hoyer’s or PVA-Lactic Acid (BioQuip Products, Inc.) mounting mediums. .. Embryos were viewed and digitized on an Eclipse microscope (Nikon) equipped with a Photonics camera. ..

    Article Title: CU06-1004 alleviates oxidative stress and inflammation on folic acid-induced acute kidney injury in mice.
    Article Snippet: For immunohistochemical analyses, samples were incubated with primary antibodies against F4/80 (Bio-Rad, Hercules, CA, USA), kidney injury molecule-1 (KIM-1) (NBP1-76701, NOVUS, Abingdon, UK), and 4-hydroxynonenal (4-HNE) (R&D Systems, MAB3249). .. Images were captured using an eclipse microscope (Nikon, Tokyo, Japan), and the F4/80-, KIM-1-, and 4-HNE-positive areas were quantified using ImageJ software (National Institutes of Health, Bethesda, Maryland, USA). .. For protein extraction, the renal samples were homogenized in radioimmunoprecipitation assay buffer (0.5 % NP-40 buffer, 50 mM β-glycerophosphate, 0.5 % NaF, 50 mM Na3VO4, 1 % Triton X-100, 0.5 % sodium deoxycholate, 1 M Tris-HCl, 50 mM NaCl, and 5 mM EDTA) containing a protease and phosphatase inhibitor cocktail (Thermo Scientific, Waltham, MA, USA).

    Article Title: Single-cell genetic analysis validates cytopathological identification of circulating cancer cells in patients with clear cell renal cell carcinoma
    Article Snippet: .. Laser microdissection of each individual cell selected was performed using an Eclipse microscope (Nikon, Japan) equipped with the Cell Cut System (Molecular Machines and Industries, Germany). ..

    Article Title: CU06-1004 modulates the adenosine monophosphate (AMP)-associated protein kinase (AMPK) signaling pathway and inhibits lipogenesis in 3T3-L1 adipocytes and high-fat diet-induced obese mice.
    Article Snippet: Aims: The endothelial dysfunction blocker CU06-1004 exhibits anti-inflammatory effects in chronic diseases.. Obesity is a major cause of chronic inflammation, and the effect of CU06-1004 on obesity has not been studied yet.. Therefore, in this study, we investigated the anti-obesity properties of CU06-1004 in 3T3-L1 adipocytes and high-fat diet-induced obese mice.

    Article Title: Biological effect of ribosomal protein L32 on human breast cancer cell behavior.
    Article Snippet: .. The stained tissue microarray samples were assessed using an ecliPSe microscope (nikon corporation) and scored with a semi-quantitative scale by two independent blinded investigators. ..

    Laser Capture Microdissection:

    Article Title: Single-cell genetic analysis validates cytopathological identification of circulating cancer cells in patients with clear cell renal cell carcinoma
    Article Snippet: .. Laser microdissection of each individual cell selected was performed using an Eclipse microscope (Nikon, Japan) equipped with the Cell Cut System (Molecular Machines and Industries, Germany). ..

    Staining:

    Article Title: Biological effect of ribosomal protein L32 on human breast cancer cell behavior.
    Article Snippet: .. The stained tissue microarray samples were assessed using an ecliPSe microscope (nikon corporation) and scored with a semi-quantitative scale by two independent blinded investigators. ..

    Microarray:

    Article Title: Biological effect of ribosomal protein L32 on human breast cancer cell behavior.
    Article Snippet: .. The stained tissue microarray samples were assessed using an ecliPSe microscope (nikon corporation) and scored with a semi-quantitative scale by two independent blinded investigators. ..



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    Image Search Results


    Synthesis and characterization of BA-HPCS@CGRP microspheres based on microfluidic fabrication. A. Fourier transform infrared spectroscopy spectra of the HPCS, 3-Carboxyphenylboronic acid (BA), and BA-HPCS. B. The hydrogel precursors appear as a liquid macroscopically before gelation. C. The hydrogels appear milky white after photo-crosslinking. D. The imaging of BA-HPCS@CGRP microspheres based on microfluidic chips: macroscopic and microscopic observations. E. Particle size distribution of BA-HPCS@CGRP microspheres. F and G. Representative scanning electron microscope images of BA-HPCS@CGRP microspheres. H. The pore size distribution of lyophilized BA-HPCS@CGRP microspheres. I. The releasing of CGRP from BA-HPCS@CGRP in PBS and different glucose conditions (100 mg/dL, 400 mg/dL). J. Representative live/dead fluorescence images of L929 cells after co-culture with microspheres (green calcein-AM for live cells, red propidium iodide for dead cells). K. The quantitative analysis of L929 cell viability co-cultured with microspheres. ns, no significance. ∗∗∗ p < 0.001; ∗∗ p < 0.01; ∗ p < 0.05; ns, no significance. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Materials Today Bio

    Article Title: Sustained-release CGRP microspheres accelerate diabetic wound healing by synergistically promoting neurovascular regeneration through modulation of macrophage and endothelial cell functions

    doi: 10.1016/j.mtbio.2026.103015

    Figure Lengend Snippet: Synthesis and characterization of BA-HPCS@CGRP microspheres based on microfluidic fabrication. A. Fourier transform infrared spectroscopy spectra of the HPCS, 3-Carboxyphenylboronic acid (BA), and BA-HPCS. B. The hydrogel precursors appear as a liquid macroscopically before gelation. C. The hydrogels appear milky white after photo-crosslinking. D. The imaging of BA-HPCS@CGRP microspheres based on microfluidic chips: macroscopic and microscopic observations. E. Particle size distribution of BA-HPCS@CGRP microspheres. F and G. Representative scanning electron microscope images of BA-HPCS@CGRP microspheres. H. The pore size distribution of lyophilized BA-HPCS@CGRP microspheres. I. The releasing of CGRP from BA-HPCS@CGRP in PBS and different glucose conditions (100 mg/dL, 400 mg/dL). J. Representative live/dead fluorescence images of L929 cells after co-culture with microspheres (green calcein-AM for live cells, red propidium iodide for dead cells). K. The quantitative analysis of L929 cell viability co-cultured with microspheres. ns, no significance. ∗∗∗ p < 0.001; ∗∗ p < 0.01; ∗ p < 0.05; ns, no significance. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Following the incubation, fluorescence images were captured using a Nikon inverted fluorescence microscope (Nikon, Japan, Modle: Eclipse Ti2-E).

    Techniques: Fourier Transform Infrared Spectroscopy, Spectroscopy, Imaging, Microscopy, Pore Size, Fluorescence, Co-Culture Assay, Cell Culture