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acquisition software zen  (Carl Zeiss)


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    Carl Zeiss acquisition software zen
    Acquisition Software Zen, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 94/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/position+module/ZEN+Module+Tiles+%26+Positions/pmc13672362-542-10-13
    Average 94 stars, based on 24 article reviews
    acquisition software zen - by Bioz Stars, 2026-11
    94/100 stars

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    Related Articles

    Immunofluorescence:

    Article Title: Hyperoxia shows duration-dependent effects on the lengths of cell cycle phases in fetal cortical neural stem cells
    Article Snippet: NSCs were continuously monitored by standard microscopy and bright-field images were taken using an Axio Imager.A1 (Carl Zeiss, Oberkochen, Germany) with ×10 objective after 7 days of cultivation within the respective oxygen condition. .. Immunofluorescence images were taken with an Axio Observer.Z1 microscope using a ×20 objective and ZEN blue software with the Tiles and Position module (Carl Zeiss). ..

    Microscopy:

    Article Title: Hyperoxia shows duration-dependent effects on the lengths of cell cycle phases in fetal cortical neural stem cells
    Article Snippet: NSCs were continuously monitored by standard microscopy and bright-field images were taken using an Axio Imager.A1 (Carl Zeiss, Oberkochen, Germany) with ×10 objective after 7 days of cultivation within the respective oxygen condition. .. Immunofluorescence images were taken with an Axio Observer.Z1 microscope using a ×20 objective and ZEN blue software with the Tiles and Position module (Carl Zeiss). ..

    Software:

    Article Title: Hyperoxia shows duration-dependent effects on the lengths of cell cycle phases in fetal cortical neural stem cells
    Article Snippet: NSCs were continuously monitored by standard microscopy and bright-field images were taken using an Axio Imager.A1 (Carl Zeiss, Oberkochen, Germany) with ×10 objective after 7 days of cultivation within the respective oxygen condition. .. Immunofluorescence images were taken with an Axio Observer.Z1 microscope using a ×20 objective and ZEN blue software with the Tiles and Position module (Carl Zeiss). ..



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    Image Search Results


    Potentiating SK channels restores normal NMDAR integration in Grin1 Y647S +/− mice (A) Schematic of potential mechanism showing impaired negative feedback in Y647S +/− neurons due to insufficient Ca 2+ influx compared to WT and the effect of NS309 in boosting SK channel Ca 2+ sensitivity, thereby restoring negative feedback in Y647S +/− neurons. (B) Average NMDAR plateau potential in Y647S +/− neurons at 70 μA with extended tail indicated by red arrow. Application of 10 μM NS309 to the slice restores normal duration and terminates the NMDAR plateau potential in Y647S +/− (Y647S +/− + NS309). (Inset) Restoration of plateau potential duration by NS309 at increasing stimulus intensities in a Y647S +/− neuron. (C) Total width of the NMDAR plateau potential in WT, Y647S +/− , and Y647S +/− + NS309 neurons (∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 10 −4 , Tukey’s post hoc. Black stars: WT vs. Y647S +/− , purple stars: Y647S +/− vs. Y647S +/− + NS309). (D) SK2 channel blocker (Leidab7, 100 nM) prevents NS309 from reducing plateau potential duration in Y647S +/− neurons. (E) Normalized NMDAR plateau width in Y647S +/− neurons with the addition of NS309 and NS309+SK2 blockers (∗ p < 0.05, Sidak’s post hoc).

    Journal: iScience

    Article Title: Context-dependent NMDA receptor dysfunction predicts seizure treatment in mice with human GluN1 variant

    doi: 10.1016/j.isci.2025.114301

    Figure Lengend Snippet: Potentiating SK channels restores normal NMDAR integration in Grin1 Y647S +/− mice (A) Schematic of potential mechanism showing impaired negative feedback in Y647S +/− neurons due to insufficient Ca 2+ influx compared to WT and the effect of NS309 in boosting SK channel Ca 2+ sensitivity, thereby restoring negative feedback in Y647S +/− neurons. (B) Average NMDAR plateau potential in Y647S +/− neurons at 70 μA with extended tail indicated by red arrow. Application of 10 μM NS309 to the slice restores normal duration and terminates the NMDAR plateau potential in Y647S +/− (Y647S +/− + NS309). (Inset) Restoration of plateau potential duration by NS309 at increasing stimulus intensities in a Y647S +/− neuron. (C) Total width of the NMDAR plateau potential in WT, Y647S +/− , and Y647S +/− + NS309 neurons (∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 10 −4 , Tukey’s post hoc. Black stars: WT vs. Y647S +/− , purple stars: Y647S +/− vs. Y647S +/− + NS309). (D) SK2 channel blocker (Leidab7, 100 nM) prevents NS309 from reducing plateau potential duration in Y647S +/− neurons. (E) Normalized NMDAR plateau width in Y647S +/− neurons with the addition of NS309 and NS309+SK2 blockers (∗ p < 0.05, Sidak’s post hoc).

    Article Snippet: SK channel positive allosteric modulator NS309 (10 μM, Tocris ) was included in a subset of experiments to restore appropriate duration of dendritic integration in Y647S +/− mice.

    Techniques: