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inverted microscope nikon eclipse te2000–5  (Nikon)


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    Nikon inverted microscope nikon eclipse te2000–5
    Inverted Microscope Nikon Eclipse Te2000–5, 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/pmc11587867-90-2-3
    Average 90 stars, based on 1 article reviews
    inverted microscope nikon eclipse te2000–5 - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: SLC7A1 , SGK1 and HMGB2 are overexpressed in cervical cancer tissues and the miR-23b-3p/HMGB2 axis regulates cell migration and invasion
    Article Snippet: Images of invading cells were obtained with an inverted microscope (Eclipse TS2; Nikon Corporation) with 10X objective.

    Article Title: Transcriptomic signatures of neonatal acute respiratory distress syndrome in a prospective cohort of respiratory distress
    Article Snippet: Images were captured using a Nikon DS-U microscope (Tokyo, Japan).

    Article Title: A novel defined manganese metabolism-related gene signature for predicting the prognosis of pancreatic ductal adenocarcinoma
    Article Snippet: Wound closure was observed under a microscope (Nikon Eclipse Ts2; Nikon Corporation) and images were captured at 0, 24 and 48 h post-scratch.

    Article Title: Inhibition of gastric adenocarcinoma proliferation by WSGC@MS: Role of KEAP1/NRF2 signaling pathway and autophagy regulation
    Article Snippet: The TUNEL assay was performed using the TUNEL apoptosis detection kit (S7100, Sigma-Aldrich, USA) following the manufacturer's instructions to confirm in situ cell apoptosis on 5 μm-thick paraffin sections.

    Article Title: SLC7A1 , SGK1 and HMGB2 are overexpressed in cervical cancer tissues and the miR-23b-3p/HMGB2 axis regulates cell migration and invasion
    Article Snippet: The culture medium was replaced every 24 h. Images of wound closure were captured with an inverted microscope (Eclipse TS2; Nikon Corporation) at magnification, ×10 at 0, 12, 24, 24, 36 and 48 h after scratching.

    Article Title: Integrative machine learning reveals the biological function and prognostic significance of α-ketoglutarate in gastric cancer
    Article Snippet: The MitoTracker staining of both groups was assessed under a microscope (TI-S; Nikon Corporation), and the MitoTracker staining intensity of both groups was further analyzed using ImageJ software (V1.8.0; National Institutes of Health).

    Article Title: M Ⅱ -polyphosphate-based wax-like material with osteogenesis and blood occlusion
    Article Snippet: Mineralized particles were visualized using an inverted microscope (Nikon, Japan).

    Microscopy:

    Article Title: Sulfhydryl-functionalized anisotropic photonic crystal hydrogels for visual Hg 2+ detection and adsorption in cinnabar mine water area.
    Article Snippet: Emissions of mercury ions from human activities during mining and smelting processes cannot be overlooked due to their potential for environmental pollution.. Consequently, developing a material that offers both visual detection capability and efficient adsorption for Hg2+ is crucial.. Inspired by cephalopod skin, we have prepared a sulfhydryl-functionalized anisotropic photonic crystal hydrogel (PDGI/PAAm-SH).



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    (A) Representative <t>epifluorescence</t> 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/ .
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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