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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 978 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/axio+observer+inverted+microscope/Inverted+microscope+Axio+Observer+7/pmc12951291-10-7-80
    Average 98 stars, based on 978 article reviews
    axio observer 7 - by Bioz Stars, 2026-09
    98/100 stars

    Images

    Related Articles

    Inverted Microscopy:

    Article Title: Sex differences in arterial stiffness in a rat model of type 1 diabetes
    Article Snippet: In brief, force-indentation curves were obtained in aortic cryosections (10 μm thickness) using the JPK ForceRobot 300 AFM instrument (Bruker, Billerica, MA, USA) coupled with the Bruker Scanasyst-Fluid probes (tip radius: 20 nm, spring constant: 0.7 N/m, resonance frequency: 150 kHz). .. The scanning location was determined with the ZEISS Axio Observer inverted microscope (Dublin, CA, USA). ..

    Article Title: Galectin-1/ galectin-3 chimeras and multivalent proteins
    Article Snippet: .. To evaluate agglutination, cells were incubated with G1, G1-PEG-G1, G1/G3 or G1/G3 Dimer (final [G3]=5 μM or 0.5 μM) and then imaged at 4 hours using a Zeiss Axio Observer inverted microscope. .. Following imaging, cells were harvested from the wells and washed with 10 mL of cold 100 mM (3-lactose to remove bound galectins followed by centrifugation at 413×g for 7 min on a Centrifuge 5804R (Eppendorf).

    Article Title: Galectin-1/ galectin-3 chimeras and multivalent proteins
    Article Snippet: .. Brightfield images of samples allowed to settle for 15 minutes were then collected using a Zeiss Axio Observer inverted microscope. .. To determine if turbidity changes were due to specific glycoprotein-galectin interactions, 50 μL PBS with or without 10 μM G1/G3 dimer was mixed 50 μL of either serum-free complete media or complete media and incubated for 10 minutes.

    Article Title: Protocol for monitoring cytoplasmic Ca 2+ dynamics using Fura Red-AM on a Zeiss Axio Observer microscope.
    Article Snippet: .. Here, we present a protocol for live-cell calcium imaging in HEK, HeLa, fibroblast, and myoblast cells using Fura Red-AM and a Zeiss Axio Observer inverted microscope. ..

    Article Title: Magnetosome organelles are organized through interactions between McaA and McaB that alter the dynamics of the bacterial actin-like protein MamK.
    Article Snippet: .. Imaging was done on a Zeiss Axio Observer Inverted microscope with Zen software (Zeiss), and images were handled using Fiji. ..

    Article Title: Graded BMP signals modulate yellow and red color in fishes, impacting adult pigment patterns and conspecific shoaling behavior.
    Article Snippet: For the whole fish imaging, fish were euthanized and captured on a Nikon D-810 digital single lens reflex camera with MicroNikkor 105 mm macro lens. .. Anal fin details were imaged using a Zeiss Axio Observer inverted microscope or Zeiss AxioZoom stereomicroscope equipped with Zeiss Axiocam cameras. .. Carotenoid autofluorescence was imaged using a Zeiss LSM880 inverted laser confocal microscope in Airyscan SR mode.

    Article Title: Rad6-mediated ubiquitination regulates the formation of Sam1-containing stress granules during nutrient stress in budding yeast.
    Article Snippet: Stress granules (SGs) are dynamic cytoplasmic structures that form in response to environmental stress and contribute to cellular adaptation.. Recent studies have shown that metabolic enzymes localize to SGs under nutrient stress; however, the molecular mechanisms regulating the assembly and organization of metabolic enzyme–containing SGs remain poorly understood.. In this study, we examined the role of ubiquitination in the regulation of SGs containing the S-adenosylmethionine synthase Sam1 in budding yeast.

    Agglutination:

    Article Title: Galectin-1/ galectin-3 chimeras and multivalent proteins
    Article Snippet: .. To evaluate agglutination, cells were incubated with G1, G1-PEG-G1, G1/G3 or G1/G3 Dimer (final [G3]=5 μM or 0.5 μM) and then imaged at 4 hours using a Zeiss Axio Observer inverted microscope. .. Following imaging, cells were harvested from the wells and washed with 10 mL of cold 100 mM (3-lactose to remove bound galectins followed by centrifugation at 413×g for 7 min on a Centrifuge 5804R (Eppendorf).

    Incubation:

    Article Title: Galectin-1/ galectin-3 chimeras and multivalent proteins
    Article Snippet: .. To evaluate agglutination, cells were incubated with G1, G1-PEG-G1, G1/G3 or G1/G3 Dimer (final [G3]=5 μM or 0.5 μM) and then imaged at 4 hours using a Zeiss Axio Observer inverted microscope. .. Following imaging, cells were harvested from the wells and washed with 10 mL of cold 100 mM (3-lactose to remove bound galectins followed by centrifugation at 413×g for 7 min on a Centrifuge 5804R (Eppendorf).

    Imaging:

    Article Title: Protocol for monitoring cytoplasmic Ca 2+ dynamics using Fura Red-AM on a Zeiss Axio Observer microscope.
    Article Snippet: .. Here, we present a protocol for live-cell calcium imaging in HEK, HeLa, fibroblast, and myoblast cells using Fura Red-AM and a Zeiss Axio Observer inverted microscope. ..

    Article Title: Magnetosome organelles are organized through interactions between McaA and McaB that alter the dynamics of the bacterial actin-like protein MamK.
    Article Snippet: .. Imaging was done on a Zeiss Axio Observer Inverted microscope with Zen software (Zeiss), and images were handled using Fiji. ..

    Software:

    Article Title: Magnetosome organelles are organized through interactions between McaA and McaB that alter the dynamics of the bacterial actin-like protein MamK.
    Article Snippet: .. Imaging was done on a Zeiss Axio Observer Inverted microscope with Zen software (Zeiss), and images were handled using Fiji. ..

    Microscopy:

    Article Title: Rad6-mediated ubiquitination regulates the formation of Sam1-containing stress granules during nutrient stress in budding yeast.
    Article Snippet: Stress granules (SGs) are dynamic cytoplasmic structures that form in response to environmental stress and contribute to cellular adaptation.. Recent studies have shown that metabolic enzymes localize to SGs under nutrient stress; however, the molecular mechanisms regulating the assembly and organization of metabolic enzyme–containing SGs remain poorly understood.. In this study, we examined the role of ubiquitination in the regulation of SGs containing the S-adenosylmethionine synthase Sam1 in budding yeast.



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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