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eclipse ti2 confocal microscope  (Nikon)


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    Structured Review

    Nikon eclipse ti2 confocal microscope
    Eclipse Ti2 Confocal Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 11952 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+ti2+confocal+microscope/ECLIPSE+Ti2/pmc12858362-119-8-12
    Average 99 stars, based on 11952 article reviews
    eclipse ti2 confocal microscope - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Fluorescence:

    Article Title: Colloid-patterned surfaces distinguish malignant mechanophenotypes
    Article Snippet: .. High-resolution fluorescence images were acquired using a Nikon ECLIPSE Ti2 confocal microscope (Nikon Corporation, Tokyo, Japan) equipped with an Orca FusionBT monochrome camera (Hamamatsu Photonics, Hamamatsu, Japan) and a CSU-W1 spinning disk unit with a 50 μm pinhole (Yokogawa Electric Corporation, Tokyo, Japan). .. The system was integrated with 405, 488, 561, and 638 nm LH + lasers and a CFI Plan Apochromat Lambda D 100 × oil immersion objective (numerical aperture 1.45, working distance 0.13 mm; Nikon Corporation, Tokyo, Japan).

    Article Title: Liquid-liquid phase separation of OsvWA36 fine-tunes brassinosteroid signaling and leaf angle in rice.
    Article Snippet: .. After 48–72 h of incubation under low light, fluorescence was imaged using a Nikon Eclipse Ti2 confocal microscope (excitation/emission: GFP 488 nm/500–550 nm; RFP 561 nm/570–620 nm) (Sparkes et al., 2006). ..

    Article Title: Aquaporin embedded suspended lipid bilayer on anodized alumina nanoporous substrates for studying stability and functionality: towards the development of a miniaturized water purifier
    Article Snippet: .. For detailed fluorescence analysis, lipid bilayers doped with Texas Red DHPE and proteins labelled with Alexa FluorTM 488 NHS ester (succinimidyl ester) were visualized using a Nikon Eclipse Ti2 confocal microscope. ..

    Microscopy:

    Article Title: Colloid-patterned surfaces distinguish malignant mechanophenotypes
    Article Snippet: .. High-resolution fluorescence images were acquired using a Nikon ECLIPSE Ti2 confocal microscope (Nikon Corporation, Tokyo, Japan) equipped with an Orca FusionBT monochrome camera (Hamamatsu Photonics, Hamamatsu, Japan) and a CSU-W1 spinning disk unit with a 50 μm pinhole (Yokogawa Electric Corporation, Tokyo, Japan). .. The system was integrated with 405, 488, 561, and 638 nm LH + lasers and a CFI Plan Apochromat Lambda D 100 × oil immersion objective (numerical aperture 1.45, working distance 0.13 mm; Nikon Corporation, Tokyo, Japan).

    Article Title: Projection targeting with phototagging to study the structure and function of retinal ganglion cells.
    Article Snippet: .. Retinas were examined using a Nikon Eclipse Ti2 confocal microscope, controlled by NIS-Elements AR software (Nikon Instruments Inc., Melville, NY, U.S.A.). ..

    Article Title: Anti-inflammatory and pro-proliferative effects of fasudil in human trisomy 21 neural progenitor cells
    Article Snippet: .. Cells were imaged at 20 X using a Nikon Eclipse Ti2 confocal microscope. ..

    Article Title: Liquid-liquid phase separation of OsvWA36 fine-tunes brassinosteroid signaling and leaf angle in rice.
    Article Snippet: .. After 48–72 h of incubation under low light, fluorescence was imaged using a Nikon Eclipse Ti2 confocal microscope (excitation/emission: GFP 488 nm/500–550 nm; RFP 561 nm/570–620 nm) (Sparkes et al., 2006). ..

    Article Title: Antibody recycling via FcRn drives atherosclerotic plaque vulnerability
    Article Snippet: For immunofluorescence, acetone-fixed cryosections were stained with fluorescent secondary antibodies for 60 minutes at room temperature, followed by 4′,6-diamidino-2-phenylindole nuclear staining (D1306, Invitrogen) and mounting in Fluorescent Mounting Medium (Dako). .. Images were acquired using a Nikon Eclipse Ti2 confocal microscope. .. For collagen quantification, deparaffinized sections were stained with 0.1% Picrosirius Red (Histolab) and rinsed in 0.5% acetic acid before air-drying.

    Article Title: Aquaporin embedded suspended lipid bilayer on anodized alumina nanoporous substrates for studying stability and functionality: towards the development of a miniaturized water purifier
    Article Snippet: .. For detailed fluorescence analysis, lipid bilayers doped with Texas Red DHPE and proteins labelled with Alexa FluorTM 488 NHS ester (succinimidyl ester) were visualized using a Nikon Eclipse Ti2 confocal microscope. ..

    Article Title: Heat shock protein 40 enhances axon regeneration in a mouse model of traumatic optic neuropathy
    Article Snippet: .. Cleared optic nerves were examined using a Nikon Eclipse Ti2 confocal microscope (Melville, NY, USA) by scanning through individual optical slices. .. Cleared optic nerves were examined using a Nikon Eclipse Ti2 confocal microscope (Melville, NY, USA) by scanning through individual optical slices.

    Article Title: Projection targeting with phototagging to study the structure and function of retinal ganglion cells
    Article Snippet: .. Retinas were examined using a Nikon Eclipse Ti2 confocal microscope, controlled by NIS-Elements AR software (Nikon Instruments Inc., Melville, NY, U.S.A.). ..

    Software:

    Article Title: Projection targeting with phototagging to study the structure and function of retinal ganglion cells.
    Article Snippet: .. Retinas were examined using a Nikon Eclipse Ti2 confocal microscope, controlled by NIS-Elements AR software (Nikon Instruments Inc., Melville, NY, U.S.A.). ..

    Article Title: Projection targeting with phototagging to study the structure and function of retinal ganglion cells
    Article Snippet: .. Retinas were examined using a Nikon Eclipse Ti2 confocal microscope, controlled by NIS-Elements AR software (Nikon Instruments Inc., Melville, NY, U.S.A.). ..

    Incubation:

    Article Title: Liquid-liquid phase separation of OsvWA36 fine-tunes brassinosteroid signaling and leaf angle in rice.
    Article Snippet: .. After 48–72 h of incubation under low light, fluorescence was imaged using a Nikon Eclipse Ti2 confocal microscope (excitation/emission: GFP 488 nm/500–550 nm; RFP 561 nm/570–620 nm) (Sparkes et al., 2006). ..



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    Image Search Results


    Preparation and characterization of ANCM@SHM. (a) Schematic diagram of NCM preparation. (b) Representative TEM images of native CM and NCM. Bar: 50 nm. (c–d) Zeta potential (n = 3), particle size (n = 3), and PDI (n = 3) of native CM and NCM measured by DLS. (e) Representative TEM images of Lipo, A-lipo, and ANCM. Bar: 50 nm. (f–g) Zeta potential (n = 3), particle size (n = 3), and PDI (n = 3) of Lipo, A-lipo, and ANCM measured by DLS. (h) Representative confocal fluorescence micrographs showing red fluorescently labeled A-lipo and green fluorescently labeled NCM fusing into gold fluorescent ANCM. Bar: 10 μm. (i) Quantification of NKG2D on the surface of CM, NCM, and ANCM nanoparticles by flow cytometry. (j–k) Encapsulation efficiency (EE) (n = 3) and loading efficiency (LE) (n = 3) of ABT263. (l) Representative SEM image of ANCM@SHM. Bar: 100 μm. (m) Representative fluorescence image of PKH67-ANCM@SHM captured by confocal microscope. Bar: 100 μm.

    Journal: Bioactive Materials

    Article Title: Injectable microgels carrying engineered biomimetic nanoparticles for osteoarthritis therapy via dual-targeted senescent chondrocyte clearance and endogenous repair promotion

    doi: 10.1016/j.bioactmat.2025.11.038

    Figure Lengend Snippet: Preparation and characterization of ANCM@SHM. (a) Schematic diagram of NCM preparation. (b) Representative TEM images of native CM and NCM. Bar: 50 nm. (c–d) Zeta potential (n = 3), particle size (n = 3), and PDI (n = 3) of native CM and NCM measured by DLS. (e) Representative TEM images of Lipo, A-lipo, and ANCM. Bar: 50 nm. (f–g) Zeta potential (n = 3), particle size (n = 3), and PDI (n = 3) of Lipo, A-lipo, and ANCM measured by DLS. (h) Representative confocal fluorescence micrographs showing red fluorescently labeled A-lipo and green fluorescently labeled NCM fusing into gold fluorescent ANCM. Bar: 10 μm. (i) Quantification of NKG2D on the surface of CM, NCM, and ANCM nanoparticles by flow cytometry. (j–k) Encapsulation efficiency (EE) (n = 3) and loading efficiency (LE) (n = 3) of ABT263. (l) Representative SEM image of ANCM@SHM. Bar: 100 μm. (m) Representative fluorescence image of PKH67-ANCM@SHM captured by confocal microscope. Bar: 100 μm.

    Article Snippet: Furthermore, for fluorescence imaging, cells were incubated with LysoTracker (Servicebio, China) for 30 min, fixed with 4 % paraformaldehyde, counterstained with phalloidine (Beyotime, China) and DAPI (Beyotime, China), and imaged using a confocal microscope (Nikon Eclipse Ti2, Japan).

    Techniques: Zeta Potential Analyzer, Fluorescence, Labeling, Flow Cytometry, Encapsulation, Microscopy