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axio observer 7  (Carl Zeiss)


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    Structured Review

    Carl Zeiss axio observer 7
    Axio Observer 7, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 98/100, based on 982 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/axio+observer+7+inverted+microscope/Inverted+microscope+Axio+Observer+7/pmc12951291-10-7-80
    Average 98 stars, based on 982 article reviews
    axio observer 7 - by Bioz Stars, 2026-09
    98/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Visual Function Correlates More Strongly with Glial Coverage than Axon Count Across Multiple Mouse Strains
    Article Snippet: .. One-micron thick cross-sections were cut and stained with p-phenylenediamine (PPD) to visualize myelin sheaths and degenerating axons under bright-field microscopy using a ZEISS Axio observer 7 inverted microscope (Carl Zeiss, Jena, Germany). ..

    Microscopy:

    Article Title: Visual Function Correlates More Strongly with Glial Coverage than Axon Count Across Multiple Mouse Strains
    Article Snippet: .. One-micron thick cross-sections were cut and stained with p-phenylenediamine (PPD) to visualize myelin sheaths and degenerating axons under bright-field microscopy using a ZEISS Axio observer 7 inverted microscope (Carl Zeiss, Jena, Germany). ..

    Article Title: Chemotaxis and selective interactions of Trichomonas vaginalis with the vaginal bacteria
    Article Snippet: .. Fixed samples were mounted using FluoromountTM and examined by fluorescence microscopy using a Zeiss Axio Observer 7 inverted microscope (Zeiss). ..

    Inverted Microscopy:

    Article Title: Visual Function Correlates More Strongly with Glial Coverage than Axon Count Across Multiple Mouse Strains
    Article Snippet: .. One-micron thick cross-sections were cut and stained with p-phenylenediamine (PPD) to visualize myelin sheaths and degenerating axons under bright-field microscopy using a ZEISS Axio observer 7 inverted microscope (Carl Zeiss, Jena, Germany). ..

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes.
    Article Snippet: .. The Zeiss Axio Observer 7 inverted microscope (Zeiss Group, Germany) was used for live cell imaging to capture the migratory paths of the PBMCs. ..

    Article Title: Local RhoA activation induces anillin-independent septin recruitment in interphase cells
    Article Snippet: The regulation of the actin cytoskeleton is key for controlling cell shape and structure.. While the Rho GTPase RhoA is well known to regulate the actomyosin cytoskeleton, its function in controlling the septin cytoskeleton remains unclear.. As RhoA interactions can vary in both time and space, they can be challenging to discern from traditional bulk biochemical assays.

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes
    Article Snippet: .. The Zeiss Axio Observer 7 inverted microscope (Zeiss Group, Germany) was used for live cell imaging to capture the migratory paths of the PBMCs. ..

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes
    Article Snippet: .. Imaging was performed using the Zeiss Axio Observer 7 inverted microscope (Zeiss Group, Germany) at 40× magnification using the green, fluorescent channel/FITC channel (excitation 494 nm/emission 506 nm). ..

    Article Title: 5′untranslated regions provide a versatile toolkit for tunable exogenous protein expression
    Article Snippet: After adhering to the glass slide for 1 h, cells were loaded with 10 μg/ml Fura 2-AM (ION Biosciences) in physiological Ringer's solution (in mM: 120 NaCl, 5 KCl, 2 CaCl 2 , 25 NaHCO 3 , 1 MgCl 2 , 5.5 HEPES, 1 D-glucose, pH 7.4; Boston BioProducts) with 0.025% Pluronic F-127 (Sigma) and 1% DMSO, and incubated for 45 min at 37°C, then rinsed twice with Ringer's solution. .. Ratiometric Ca 2+ imaging was performed using a Zeiss Axio Observer 7 inverted microscope with a Hamamatsu Flash sCMOS camera at a 20× objective. ..

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes.
    Article Snippet: .. Imaging was performed using the Zeiss Axio Observer 7 inverted microscope (Zeiss Group, Germany) at 40× magnification using the green, fluorescent channel/FITC channel (excitation 494 nm/emission 506 nm). ..

    Live Cell Imaging:

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes.
    Article Snippet: .. The Zeiss Axio Observer 7 inverted microscope (Zeiss Group, Germany) was used for live cell imaging to capture the migratory paths of the PBMCs. ..

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes
    Article Snippet: .. The Zeiss Axio Observer 7 inverted microscope (Zeiss Group, Germany) was used for live cell imaging to capture the migratory paths of the PBMCs. ..

    Imaging:

    Article Title: Local RhoA activation induces anillin-independent septin recruitment in interphase cells
    Article Snippet: The regulation of the actin cytoskeleton is key for controlling cell shape and structure.. While the Rho GTPase RhoA is well known to regulate the actomyosin cytoskeleton, its function in controlling the septin cytoskeleton remains unclear.. As RhoA interactions can vary in both time and space, they can be challenging to discern from traditional bulk biochemical assays.

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes
    Article Snippet: .. Imaging was performed using the Zeiss Axio Observer 7 inverted microscope (Zeiss Group, Germany) at 40× magnification using the green, fluorescent channel/FITC channel (excitation 494 nm/emission 506 nm). ..

    Article Title: 5′untranslated regions provide a versatile toolkit for tunable exogenous protein expression
    Article Snippet: After adhering to the glass slide for 1 h, cells were loaded with 10 μg/ml Fura 2-AM (ION Biosciences) in physiological Ringer's solution (in mM: 120 NaCl, 5 KCl, 2 CaCl 2 , 25 NaHCO 3 , 1 MgCl 2 , 5.5 HEPES, 1 D-glucose, pH 7.4; Boston BioProducts) with 0.025% Pluronic F-127 (Sigma) and 1% DMSO, and incubated for 45 min at 37°C, then rinsed twice with Ringer's solution. .. Ratiometric Ca 2+ imaging was performed using a Zeiss Axio Observer 7 inverted microscope with a Hamamatsu Flash sCMOS camera at a 20× objective. ..

    Article Title: Autologous Blood Clot Therapy for Wounds: Investigating the Chemotactic Effect on PBMCs and Fibroblasts in Diabetes.
    Article Snippet: .. Imaging was performed using the Zeiss Axio Observer 7 inverted microscope (Zeiss Group, Germany) at 40× magnification using the green, fluorescent channel/FITC channel (excitation 494 nm/emission 506 nm). ..

    Fluorescence:

    Article Title: Chemotaxis and selective interactions of Trichomonas vaginalis with the vaginal bacteria
    Article Snippet: .. Fixed samples were mounted using FluoromountTM and examined by fluorescence microscopy using a Zeiss Axio Observer 7 inverted microscope (Zeiss). ..



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    Synthesis and characterization of BA-HPCS@CGRP microspheres based on microfluidic fabrication. A. Fourier transform infrared spectroscopy spectra of the HPCS, 3-Carboxyphenylboronic acid (BA), and BA-HPCS. B. The hydrogel precursors appear as a liquid macroscopically before gelation. C. The hydrogels appear milky white after photo-crosslinking. D. The imaging of BA-HPCS@CGRP microspheres based on microfluidic chips: macroscopic and microscopic observations. E. Particle size distribution of BA-HPCS@CGRP microspheres. F and G. Representative scanning electron <t>microscope</t> images of BA-HPCS@CGRP microspheres. H. The pore size distribution of lyophilized BA-HPCS@CGRP microspheres. I. The releasing of CGRP from BA-HPCS@CGRP in PBS and different glucose conditions (100 mg/dL, 400 mg/dL). J. Representative live/dead <t>fluorescence</t> images of L929 cells after co-culture with microspheres (green calcein-AM for live cells, red propidium iodide for dead cells). K. The quantitative analysis of L929 cell viability co-cultured with microspheres. ns, no significance. ∗∗∗ p < 0.001; ∗∗ p < 0.01; ∗ p < 0.05; ns, no significance. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Image Search Results


    Synthesis and characterization of BA-HPCS@CGRP microspheres based on microfluidic fabrication. A. Fourier transform infrared spectroscopy spectra of the HPCS, 3-Carboxyphenylboronic acid (BA), and BA-HPCS. B. The hydrogel precursors appear as a liquid macroscopically before gelation. C. The hydrogels appear milky white after photo-crosslinking. D. The imaging of BA-HPCS@CGRP microspheres based on microfluidic chips: macroscopic and microscopic observations. E. Particle size distribution of BA-HPCS@CGRP microspheres. F and G. Representative scanning electron microscope images of BA-HPCS@CGRP microspheres. H. The pore size distribution of lyophilized BA-HPCS@CGRP microspheres. I. The releasing of CGRP from BA-HPCS@CGRP in PBS and different glucose conditions (100 mg/dL, 400 mg/dL). J. Representative live/dead fluorescence images of L929 cells after co-culture with microspheres (green calcein-AM for live cells, red propidium iodide for dead cells). K. The quantitative analysis of L929 cell viability co-cultured with microspheres. ns, no significance. ∗∗∗ p < 0.001; ∗∗ p < 0.01; ∗ p < 0.05; ns, no significance. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Materials Today Bio

    Article Title: Sustained-release CGRP microspheres accelerate diabetic wound healing by synergistically promoting neurovascular regeneration through modulation of macrophage and endothelial cell functions

    doi: 10.1016/j.mtbio.2026.103015

    Figure Lengend Snippet: Synthesis and characterization of BA-HPCS@CGRP microspheres based on microfluidic fabrication. A. Fourier transform infrared spectroscopy spectra of the HPCS, 3-Carboxyphenylboronic acid (BA), and BA-HPCS. B. The hydrogel precursors appear as a liquid macroscopically before gelation. C. The hydrogels appear milky white after photo-crosslinking. D. The imaging of BA-HPCS@CGRP microspheres based on microfluidic chips: macroscopic and microscopic observations. E. Particle size distribution of BA-HPCS@CGRP microspheres. F and G. Representative scanning electron microscope images of BA-HPCS@CGRP microspheres. H. The pore size distribution of lyophilized BA-HPCS@CGRP microspheres. I. The releasing of CGRP from BA-HPCS@CGRP in PBS and different glucose conditions (100 mg/dL, 400 mg/dL). J. Representative live/dead fluorescence images of L929 cells after co-culture with microspheres (green calcein-AM for live cells, red propidium iodide for dead cells). K. The quantitative analysis of L929 cell viability co-cultured with microspheres. ns, no significance. ∗∗∗ p < 0.001; ∗∗ p < 0.01; ∗ p < 0.05; ns, no significance. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Following the 30 - min incubation in the dark, images were collected with the ZEISS inverted fluorescence microscope (Carl Zeiss AG, Oberkochen, Germany; Model: Axio Observer 7).

    Techniques: Fourier Transform Infrared Spectroscopy, Spectroscopy, Imaging, Microscopy, Pore Size, Fluorescence, Co-Culture Assay, Cell Culture