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inverted fluorescence microscope  (Nikon)


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    Structured Review

    Nikon inverted fluorescence microscope
    Inverted Fluorescence 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/fluorescence+microscope+eclipse+ti2/ECLIPSE+Ti2/pmc12934279-126-14-17
    Average 99 stars, based on 11824 article reviews
    inverted fluorescence microscope - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    other:

    Article Title: Inhibition of EHMT1/2 rescues synaptic damage and motor impairment in a PD mouse model
    Article Snippet: Images were taken with a fluorescence microscope (ECLIPSE Ti2, Nikon) and then processed and counted with Photoshop software (Adobe) and Fiji software (National Institutes of Health).

    Article Title: Patient-Derived Organoids on a Microarray for Drug Resistance Study in Breast Cancer.
    Article Snippet: After washing with PBS, the cells were observed directly under the fluorescence microscope (ECLIPSE Ti2, Nikon, Japan).

    Article Title: Design, synthesis and biological evaluation of Nrf2 modulators for the treatment of glioblastoma multiforme.
    Article Snippet: Glioblastoma multiforme (GBM) is a prevalent primary brain tumor.. However, no specific therapeutic drug has been developed for it.. Nuclear factor erythroid 2related factor 2 (Nrf2) is a crucial transcription factor involved in the cellular response to oxidative stress.

    Article Title: Artificial Vascular with Pressure-Responsive Property based on Deformable Microfluidic Channels.
    Article Snippet: In vitro blood vessel models are significant for disease modeling, drug assays, and therapeutic development.. Microfluidic technologies allow creating physiologically relevant culture models reproducing the features of the in vivo vascular microenvironment.. However, current microfluidic technologies are limited by impractical rectangular cross-sections and single or nonsynchronous compound mechanical stimuli.

    Article Title: α-Mangostin suppresses ethanol-induced gastric ulceration by regulating the Nrf2/HO-1 and NF-κB/NLRP3/caspase-1 signaling pathways and gut microbiota
    Article Snippet: The cells were observed using a fluorescence microscope (ECLIPSE Ti2; Nikon, Japan).

    Article Title: Analysis of Haemonchus embryos at single cell resolution identifies two eukaryotic elongation factors as intervention target candidates
    Article Snippet: Subsequently, the pellet of nuclei was resuspended in 500 μl of ice-cold nuclei wash buffer with 10 μg/ml DAPI (4,6-diamidino-2-phenylindole; Sigma-Aldrich, USA) and an aliquot (5 μl) thereof examined at 300-times magnification using a fluorescence microscope (ECLIPSE Ti2 Nikon, Japan) to appraise the shape and size of the cell nuclei.

    Article Title: Lgr6-expressing functional nail stem-like cells differentiated from human-induced pluripotent stem cells.
    Article Snippet: After washing three times, fluorescent signals were observed using a fluorescence microscope (Eclipse Ti2, Nikon Instruments, Tokyo, Japan) controlled by the equipped software (NIS-Elements, Nikon Instruments).

    Fluorescence:

    Article Title: PCAF promotes R-loop resolution via histone acetylation.
    Article Snippet: Cells were then incubated with Alexa Fluor econdary antibody in 3% BSA / PBST for 1 h and mounted ith Vectashield mounting medium containing DAPI (Vector abs). .. Images were captured using a fluorescence microscope Eclipse Ti2, Nikon) or Fluoview FV 3000 confocal microcope (Olympus) and nucleoplasmic S9.6 signals were quanified using ImageJ. ..

    Microscopy:

    Article Title: PCAF promotes R-loop resolution via histone acetylation.
    Article Snippet: Cells were then incubated with Alexa Fluor econdary antibody in 3% BSA / PBST for 1 h and mounted ith Vectashield mounting medium containing DAPI (Vector abs). .. Images were captured using a fluorescence microscope Eclipse Ti2, Nikon) or Fluoview FV 3000 confocal microcope (Olympus) and nucleoplasmic S9.6 signals were quanified using ImageJ. ..



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    Nikon nikon inverted fluorescence microscope
    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 <t>microscope</t> 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 <t>fluorescence</t> 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.)
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    99
    Nikon fluorescence microscope
    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 <t>microscope</t> 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 <t>fluorescence</t> 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.)
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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