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high resolution optical microscope zeiss axiotech 100hd  (Carl Zeiss)


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    Carl Zeiss high resolution optical microscope zeiss axiotech 100hd
    High Resolution Optical Microscope Zeiss Axiotech 100hd, supplied by Carl Zeiss, 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/axiotech+microscope/auriga+electron+microscope+scanning+zeiss/us12344921-2707-10-13
    Average 90 stars, based on 1 article reviews
    high resolution optical microscope zeiss axiotech 100hd - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Microscopy:

    Article Title: Temporo-Spectral Imaging of Intrinsic Optical Signals during Hypoxia-Induced Spreading Depression-Like Depolarization
    Article Snippet: .. With an 100 ms delay implemented in between the single wavelength exposures, an illumination spectrum was acquired within ∼2.4 s. Slices were illuminated at an angle of 45° and illumination spectra were recorded every 15 s. Slices were viewed with a 5x, 0.13NA objective (Epiplan, Zeiss) and an Axiotech microscope (Zeiss). ..

    Article Title: Generation of Connective Tissue-Free Microvascular Fragment Isolates from Subcutaneous Fat Tissue of Obese Mice.
    Article Snippet: For this purpose, 0.1 mL of the blood plasma marker 5% fluorescein isothiocyanate (FITC)-labeled dextran (150,000 Da; Sigma-Aldrich) was injected into the retrobulbar venous plexus of the anesthetized animals for contrast enhancement. .. The observation window of the dorsal skinfold chamber was placed under a Zeiss Axiotech microscope (Zeiss, Oberkochen, Germany) and the microscopic images were recorded by a charge-coupled device video camera (FK6990; Pieper, Schwerte, Germany) and a DVD system. ..

    Article Title: Real-Time Nitric Oxide and Inflammation Sensing in 2D Osteoarthritis Models: Microsensor Design and Application
    Article Snippet: Nitric oxide (NO), a key metabolite released during inflammation, can be a reliable biomarker for conditions such as trauma, infection or during inflammation.. Standard NO detection methods, including electron paramagnetic resonance (EPR) and indirect detection of nitrites as NO derivatives, using Griess assay, are limited in their ability to provide real-time monitoring, a critical feature for studying drug responses and enabling clinical applications.. Electrochemical sensors can be used for continuous real-time NO measurement but require careful design to ensure selectivity in complex biological environments.

    Article Title: Seaweed Extracts as an Effective Gateway in the Search for Novel Antibiofilm Agents against Staphylococcus aureus .
    Article Snippet: Six mL of SDW were then added supplemented with 1.0 μL of Syto9 stain (5 mM, InvitrogenTM, ThermoFisher Scientific, llkirch, France) for cell visualization. .. Microscopic observations were made with Zeiss—Axiotech microscope using a 20 ×/0.50 (Zeiss, EC Plan-Neofluar) objective and equipped with an HXP 120 C light source. .. Images were acquired with a digital camera (Zeiss AxioCam ICm 1) and then the set of photos was processed with ZEN software.

    Article Title: Coaxial electrospun nanofibers as drug delivery system for local treatment of periodontitis.
    Article Snippet: .. Green and red fluorescence of the cells, respectively, was monitored using an Axiotech microscope (Carl Zeiss, Jena, Germany) equipped with filter sets 09 and 14. ..

    Article Title: A preclinical platform for assessing long-term drug efficacy exploiting mechanically tunable scaffolds colonized by a three-dimensional tumor microenvironment
    Article Snippet: If scaffolds were used for fluorescent or confocal imaging, CAF were stained with IncuCyte® Nuclight Rapid Red Cell Labeling (4717, Sartorius). .. Optical microscopic images of printed scaffolds were obtained using an Axiotech microscope (Zeiss) using top down illumination in combination with an Axiocam for image acquisition. ..

    Article Title: A preclinical platform for assessing long-term drug efficacy exploiting mechanically tunable scaffolds colonized by a three-dimensional tumor microenvironment.
    Article Snippet: If scaffolds were used for fluorescent or confocal imaging, CAF were stained with IncuCyte® Nuclight Rapid Red Cell Labeling (4717, Sartorius). .. Optical microscopic images of printed scaffolds were obtained using an Axiotech microscope (Zeiss) using top down illumination in combination with an Axiocam for image acquisition. ..

    other:

    Article Title: Mesenchymal stem cells inhibit multiple myeloma cells via the Fas/Fas ligand pathway
    Article Snippet: The other cells were blocked with 10% normal goat serum for 30 minutes at 37°C and incubated overnight at 4°C with anti-Fas (1:100; Chemicon International Inc. Temecula, CA, USA) or anti-Fas-L (1:100; Chemicon International Inc.) antibodies.

    Light Microscopy:

    Article Title: Real-Time Nitric Oxide and Inflammation Sensing in 2D Osteoarthritis Models: Microsensor Design and Application
    Article Snippet: Nitric oxide (NO), a key metabolite released during inflammation, can be a reliable biomarker for conditions such as trauma, infection or during inflammation.. Standard NO detection methods, including electron paramagnetic resonance (EPR) and indirect detection of nitrites as NO derivatives, using Griess assay, are limited in their ability to provide real-time monitoring, a critical feature for studying drug responses and enabling clinical applications.. Electrochemical sensors can be used for continuous real-time NO measurement but require careful design to ensure selectivity in complex biological environments.

    Fluorescence:

    Article Title: Coaxial electrospun nanofibers as drug delivery system for local treatment of periodontitis.
    Article Snippet: .. Green and red fluorescence of the cells, respectively, was monitored using an Axiotech microscope (Carl Zeiss, Jena, Germany) equipped with filter sets 09 and 14. ..



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    Carl Zeiss zeiss-axiotech epifluorescence microscope
    Study of the adhesion and viability of P. aeruginosa PAO1-Tn 7-gfp on SiO 2 -samples and AgNPs-based biomaterials. Cultivable planktonic and adhered bacteria were quantified after 30 and 90 min of contact under static conditions. Results are expressed as means log CFU/cm 2 ± Standard Deviation (SD) from three independent experiments. In accordance with the applied methodology for counting the planktonic cells log CFU/cm 2 = log CFU/mL. Statistically significant differences are determined by two-way ANOVA with Tukey’ test for multiple comparisons (∗∗, p- value <0.01, ∗∗∗∗, p- value <0.0001), ns: not significant, nd: not detected. <t>Epifluorescence</t> microscopic images are presented in Supplementary Materials, .
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    Study of the adhesion and viability of P. aeruginosa PAO1-Tn 7-gfp on SiO 2 -samples and AgNPs-based biomaterials. Cultivable planktonic and adhered bacteria were quantified after 30 and 90 min of contact under static conditions. Results are expressed as means log CFU/cm 2 ± Standard Deviation (SD) from three independent experiments. In accordance with the applied methodology for counting the planktonic cells log CFU/cm 2 = log CFU/mL. Statistically significant differences are determined by two-way ANOVA with Tukey’ test for multiple comparisons (∗∗, p- value <0.01, ∗∗∗∗, p- value <0.0001), ns: not significant, nd: not detected. <t>Epifluorescence</t> microscopic images are presented in Supplementary Materials, .
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    Image Search Results


    Study of the adhesion and viability of P. aeruginosa PAO1-Tn 7-gfp on SiO 2 -samples and AgNPs-based biomaterials. Cultivable planktonic and adhered bacteria were quantified after 30 and 90 min of contact under static conditions. Results are expressed as means log CFU/cm 2 ± Standard Deviation (SD) from three independent experiments. In accordance with the applied methodology for counting the planktonic cells log CFU/cm 2 = log CFU/mL. Statistically significant differences are determined by two-way ANOVA with Tukey’ test for multiple comparisons (∗∗, p- value <0.01, ∗∗∗∗, p- value <0.0001), ns: not significant, nd: not detected. Epifluorescence microscopic images are presented in Supplementary Materials, .

    Journal: Biofilm

    Article Title: From adhesion to biofilms formation and resilience: Exploring the impact of silver nanoparticles-based biomaterials on Pseudomonas aeruginosa

    doi: 10.1016/j.bioflm.2025.100267

    Figure Lengend Snippet: Study of the adhesion and viability of P. aeruginosa PAO1-Tn 7-gfp on SiO 2 -samples and AgNPs-based biomaterials. Cultivable planktonic and adhered bacteria were quantified after 30 and 90 min of contact under static conditions. Results are expressed as means log CFU/cm 2 ± Standard Deviation (SD) from three independent experiments. In accordance with the applied methodology for counting the planktonic cells log CFU/cm 2 = log CFU/mL. Statistically significant differences are determined by two-way ANOVA with Tukey’ test for multiple comparisons (∗∗, p- value <0.01, ∗∗∗∗, p- value <0.0001), ns: not significant, nd: not detected. Epifluorescence microscopic images are presented in Supplementary Materials, .

    Article Snippet: The observations were conducted using a Zeiss-Axiotech epifluorescence microscope with a 20X (Zeiss, EC Plan-Neofluar) objective, equipped with an HXP 120 C light source, a digital camera (Zeiss AxioCam ICm 1), coupled to the ZEN software.

    Techniques: Bacteria, Standard Deviation

    Epifluorescence microscopy images of P. aeruginosa PAO1-Tn 7- gfp 72h-old biofilms formed on SiO 2 -samples (a), after application of low (0.3 Pa), medium (4.3 Pa) and very high (16.7 Pa) wall shear-stresses. Shear-flow induced detachment profiles of live and dead bacteria on SiO 2 -samples (b). The same sequence but for AgNPs-based biomaterials: epifluorescence microscopy images of P. aeruginosa PAO1-Tn 7- gfp 72h-old biofilms (c) and wall shear-stress induced detachment profiles of live and dead bacteria (d).

    Journal: Biofilm

    Article Title: From adhesion to biofilms formation and resilience: Exploring the impact of silver nanoparticles-based biomaterials on Pseudomonas aeruginosa

    doi: 10.1016/j.bioflm.2025.100267

    Figure Lengend Snippet: Epifluorescence microscopy images of P. aeruginosa PAO1-Tn 7- gfp 72h-old biofilms formed on SiO 2 -samples (a), after application of low (0.3 Pa), medium (4.3 Pa) and very high (16.7 Pa) wall shear-stresses. Shear-flow induced detachment profiles of live and dead bacteria on SiO 2 -samples (b). The same sequence but for AgNPs-based biomaterials: epifluorescence microscopy images of P. aeruginosa PAO1-Tn 7- gfp 72h-old biofilms (c) and wall shear-stress induced detachment profiles of live and dead bacteria (d).

    Article Snippet: The observations were conducted using a Zeiss-Axiotech epifluorescence microscope with a 20X (Zeiss, EC Plan-Neofluar) objective, equipped with an HXP 120 C light source, a digital camera (Zeiss AxioCam ICm 1), coupled to the ZEN software.

    Techniques: Epifluorescence Microscopy, Shear, Bacteria, Sequencing