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digital nikon ds ri2 camera  (Nikon)


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    Nikon digital nikon ds ri2 camera
    Digital Nikon Ds Ri2 Camera, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+te2000+5+microscope/DS-Ri2/pmc09414317-92-19-20
    Average 99 stars, based on 1 article reviews
    digital nikon ds ri2 camera - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Microscopy:

    Article Title: Complete biosynthesis of psychedelic tryptamines from three kingdoms in plants.
    Article Snippet: Absolute quantification of psilocin 16 and psilocybin 19 was performed in the laboratory of D. Meiri using an ultrahigh performance liquid chromatograph (UltiMate 3000) coupled to a Q Exactive Focus Hybrid Quadrupole- Orbitrap MS (Thermo Fisher Scientific, Bremen, Germany). .. Sections were imaged with a Nikon DS- Ri2 microscope. .. MALDI imaging was performed using a 7 T Solarix FT- ICR (Fourier transform ion cyclotron resonance) mass spectrometer (Bruker Daltonics).

    Article Title: Querciphoma Phyllanthi-Emblicae , a Novel Leaf Endophyte in Amla ( Phyllanthus Emblica L.) from Yunnan, China
    Article Snippet: .. Micromorphological features, viz . conidiomata, conidiogenous cells, and conidia, were examined and photo-captured by a Nikon compound microscope (model ECLIPSE N i -U, Japan) connected with a Nikon DS-Ri2 camera (Tokyo, Japan) using DIC microscopy. ..

    Article Title: Abrupt eruptive instability of ice adhered to solid surfaces.
    Article Snippet: .. The fracture dynamics of the ice plate was observed with a polarized microscope (LVDIA- N, Nikon) in conjunction with a high- speed camera (Phantom v7.3) and a digital camera (DS- Ri2, Nikon). ..

    Article Title: Complete biosynthesis of psychedelic tryptamines from three kingdoms in plants
    Article Snippet: .. Sections were imaged with a Nikon DS-Ri2 microscope. .. MALDI imaging was performed using a 7 T Solarix FT-ICR (Fourier transform ion cyclotron resonance) mass spectrometer (Bruker Daltonics).

    Article Title: Abrupt eruptive instability of ice adhered to solid surfaces
    Article Snippet: .. The fracture dynamics of the ice plate was observed with a polarized microscope (LVDIA-N, Nikon) in conjunction with a high-speed camera (Phantom v7.3) and a digital camera (DS-Ri2, Nikon). ..

    other:


    Light Microscopy:

    Article Title: Complement-inflammation inhibition via stealth nanomedicine for mild thermo-responsive postoperative on-demand pain management
    Article Snippet: .. Light microscopy images (Nikon DS-Ri2) and temperature changes (FLUKE TIS20+ infrared camera) were recorded simultaneously. ..



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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