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eclipse te2000-5 fluorescence microscope  (Nikon)


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    Structured Review

    Nikon eclipse te2000-5 fluorescence microscope
    Eclipse Te2000 5 Fluorescence Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+te2000+5+microscope/eclipse+e600+microscope/pmc06205106-128-10-9
    Average 90 stars, based on 1 article reviews
    eclipse te2000-5 fluorescence microscope - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Microscopy:


    Article Title: Tectoridin alleviates caerulein-induced severe acute pancreatitis by targeting ERK2 to promote macrophage M2 polarization.
    Article Snippet: Severe acute pancreatitis (SAP) is an inflammatory disease of the pancreas with a high mortality rate.. Macrophages play a crucial role in the pathogenesis of pancreatitis.. Tectoridin (Tec) is a highly active isoflavone with anti-inflammatory pharmacological activity.

    Article Title: Mechano-Cas12a Assisted Tension Sensor (MCATS) for Massively Amplified Cell Traction Force Measurements
    Article Snippet: .. We used a Nikon Eclipse Ti microscope, operated by Nikon Elements software, and equipped with a 1.49 numerical aperture (NA) CFI Apo ×100 objective, perfect focus system, a TIRF laser launch, a Chroma quad cube (ET-405/488/561/640 nm Laser Quad Band) and an RICM (Nikon: 97270) cube for this work. ..

    Article Title: Reconfiguration and loss of peritubular capillaries in chronic kidney disease.
    Article Snippet: .. Photographs were taken using a DS-Qi2 digital camera (Nikon Instruments, Tokyo, Japan) attached to an Eclipse 80i microscope (Nikon Instruments) and an Intensilight C-HGFI illuminator (Nikon Instruments). .. Human 2D immunofluorescence imaging Confocal imaging of CD31-stained total human kidney biopsies was performed on a Zeiss Spinning Disc Axio Z1 live cell observer (Zeiss, Jena, Germany).

    Article Title: A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formation
    Article Snippet: .. The images were captured either via a Nikon ECLIPSE 80i microscope with a DS-Ri1 camera and processed with NIS-elements BR software or by an Olympus BX53 microscope (Olympus, Tokyo, Japan) equipped with an SC-180 camera and processed with Olympus cellSens software. ..

    Article Title: Step-wise evolution of azole resistance through copy number variation followed by KSR1 loss of heterozygosity in Candida albicans
    Article Snippet: .. 3-5μL of cell culture was deposited on a glass slide topped with 10 μL of low melt agar and imaged with a Nikon Ti Eclipse microscope using the Nikon Elements AR software, and Nikon Plan Apo x100 objective. ..

    Incubation:

    Article Title: Tectoridin alleviates caerulein-induced severe acute pancreatitis by targeting ERK2 to promote macrophage M2 polarization.
    Article Snippet: Severe acute pancreatitis (SAP) is an inflammatory disease of the pancreas with a high mortality rate.. Macrophages play a crucial role in the pathogenesis of pancreatitis.. Tectoridin (Tec) is a highly active isoflavone with anti-inflammatory pharmacological activity.

    Software:

    Article Title: Mechano-Cas12a Assisted Tension Sensor (MCATS) for Massively Amplified Cell Traction Force Measurements
    Article Snippet: .. We used a Nikon Eclipse Ti microscope, operated by Nikon Elements software, and equipped with a 1.49 numerical aperture (NA) CFI Apo ×100 objective, perfect focus system, a TIRF laser launch, a Chroma quad cube (ET-405/488/561/640 nm Laser Quad Band) and an RICM (Nikon: 97270) cube for this work. ..

    Article Title: A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formation
    Article Snippet: .. The images were captured either via a Nikon ECLIPSE 80i microscope with a DS-Ri1 camera and processed with NIS-elements BR software or by an Olympus BX53 microscope (Olympus, Tokyo, Japan) equipped with an SC-180 camera and processed with Olympus cellSens software. ..

    Article Title: Step-wise evolution of azole resistance through copy number variation followed by KSR1 loss of heterozygosity in Candida albicans
    Article Snippet: .. 3-5μL of cell culture was deposited on a glass slide topped with 10 μL of low melt agar and imaged with a Nikon Ti Eclipse microscope using the Nikon Elements AR software, and Nikon Plan Apo x100 objective. ..

    Inverted Microscopy:

    Article Title: Cartilage-derived mesenchymal cell lines
    Article Snippet: .. Images were taken using a Nikon Eclipse TE2000 inverted microscope at 20× magnification. ..

    Cell Culture:

    Article Title: Step-wise evolution of azole resistance through copy number variation followed by KSR1 loss of heterozygosity in Candida albicans
    Article Snippet: .. 3-5μL of cell culture was deposited on a glass slide topped with 10 μL of low melt agar and imaged with a Nikon Ti Eclipse microscope using the Nikon Elements AR software, and Nikon Plan Apo x100 objective. ..

    other:

    Article Title: Microglial low-affinity FcγR mediates the phagocytic elimination of dopaminergic neurons in Parkinson’s disease degeneration
    Article Snippet: A bright field microscope (Eclipse 80i microscope, Nikon; Tokyo, Japan) with a connected digital camera (DXM 1200F Digital Camera, Nikon, Tokyo, Japan) was also used for taking the required sampling.



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    Image Search Results


    (A) Representative epifluorescence images (20×) of L4 animals expressing Pins-3::GFP under basal conditions (20 °C on Nematode Growth Media plates seeded with OP50), under oxidative stress (1 mM FeSO 4, 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous tyramine (15 mM). Scale bar 50 µm. (B) Corresponding quantification of fluorescence levels per worm. Scatter dot plot with relative expression of Pins-3::GFP normalized to basal conditions of each independent experiment. Line at the median. n = 50−200 animals per condition (distributed across 3–4 independent experiments). One-way ANOVA and Dunn’s post hoc test vs. basal were used. * p < 0.05, **** p < 0.0001. (C) Log 2 fold-changes in ins-3 transcript levels in animals exposed to oxidative stress (1 mM FeSO 4 , 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous Tyramine (15 mM). Negative and positive values indicate down- and up-regulation of ins-3 , respectively. Fold change was calculated as ΔCt basal conditions/ΔCt test conditions. Results are shown as mean ± s.e.m. n = 4 independent experiments. The data underlying this figure can be found at https://osf.io/wfgvs/ .

    Journal: PLOS Biology

    Article Title: The neurohormone tyramine stimulates the secretion of an insulin-like peptide from the Caenorhabditis elegans intestine to modulate the systemic stress response

    doi: 10.1371/journal.pbio.3002997

    Figure Lengend Snippet: (A) Representative epifluorescence images (20×) of L4 animals expressing Pins-3::GFP under basal conditions (20 °C on Nematode Growth Media plates seeded with OP50), under oxidative stress (1 mM FeSO 4, 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous tyramine (15 mM). Scale bar 50 µm. (B) Corresponding quantification of fluorescence levels per worm. Scatter dot plot with relative expression of Pins-3::GFP normalized to basal conditions of each independent experiment. Line at the median. n = 50−200 animals per condition (distributed across 3–4 independent experiments). One-way ANOVA and Dunn’s post hoc test vs. basal were used. * p < 0.05, **** p < 0.0001. (C) Log 2 fold-changes in ins-3 transcript levels in animals exposed to oxidative stress (1 mM FeSO 4 , 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous Tyramine (15 mM). Negative and positive values indicate down- and up-regulation of ins-3 , respectively. Fold change was calculated as ΔCt basal conditions/ΔCt test conditions. Results are shown as mean ± s.e.m. n = 4 independent experiments. The data underlying this figure can be found at https://osf.io/wfgvs/ .

    Article Snippet: For ins-3 and ins-4 expression levels analysis, animals containing the corresponding transcriptional GFP reporter ( Pins-3::GFP and Pins-4:GFP , respectively) were imaged using an epifluorescence microscope (Nikon Eclipse TE2000-5) coupled to a CCD camera (Nikon DS-Qi2) with 20× objective.

    Techniques: Expressing, Fluorescence

    Representative epifluorescence images (40×) of young not gravid adults expressing Pges-1::INS-3::VENUS in wild-type and tyra-3 null mutant background, in the absence or presence of exogenous tyramine (15 mM). Scale bar 25 µm. Fluorescence is observed in the two posterior coelomocytes of worms (inset). Right. Corresponding quantification of fluorescence intensity on the coelomocytes (normalized to wild-type animals without tyramine exposure). Line at the median. n = 35–40 animals per condition distributed across three independent experiments. For conditions with tyramine, a two-tailed Student’s t test vs. the same strain without tyramine was used. * p < 0.05. The data underlying this figure can be found at https://osf.io/wfgvs/ .

    Journal: PLOS Biology

    Article Title: The neurohormone tyramine stimulates the secretion of an insulin-like peptide from the Caenorhabditis elegans intestine to modulate the systemic stress response

    doi: 10.1371/journal.pbio.3002997

    Figure Lengend Snippet: Representative epifluorescence images (40×) of young not gravid adults expressing Pges-1::INS-3::VENUS in wild-type and tyra-3 null mutant background, in the absence or presence of exogenous tyramine (15 mM). Scale bar 25 µm. Fluorescence is observed in the two posterior coelomocytes of worms (inset). Right. Corresponding quantification of fluorescence intensity on the coelomocytes (normalized to wild-type animals without tyramine exposure). Line at the median. n = 35–40 animals per condition distributed across three independent experiments. For conditions with tyramine, a two-tailed Student’s t test vs. the same strain without tyramine was used. * p < 0.05. The data underlying this figure can be found at https://osf.io/wfgvs/ .

    Article Snippet: For ins-3 and ins-4 expression levels analysis, animals containing the corresponding transcriptional GFP reporter ( Pins-3::GFP and Pins-4:GFP , respectively) were imaged using an epifluorescence microscope (Nikon Eclipse TE2000-5) coupled to a CCD camera (Nikon DS-Qi2) with 20× objective.

    Techniques: Expressing, Mutagenesis, Fluorescence, Two Tailed Test