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zeiss primovert microscope  (Carl Zeiss)


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    Carl Zeiss zeiss primovert microscope
    Zeiss Primovert Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 1960 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/zeiss+inverted+microscope/Primovert+Compact+Inverted+Microscope/pm41832953-289-20-23
    Average 99 stars, based on 1960 article reviews
    zeiss primovert microscope - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Immortalized Rat Tendon-Derived Stem Cells for Tendon Tissue Engineering
    Article Snippet: .. Samples were observed and recorded using a Primovert inverted cell culture microscope (ZEISS, Jena, Germany) with Axiocam 208 color camera with bright-field imaging. ..

    Article Title: Immortalized Rat Tendon-Derived Stem Cells for Tendon Tissue Engineering
    Article Snippet: .. Samples were observed and recorded using a Primovert inverted cell culture microscope (ZEISS, Jena, Germany) with Axiocam 208 color camera with bright-field imaging. ..

    Microscopy:

    Article Title: Immortalized Rat Tendon-Derived Stem Cells for Tendon Tissue Engineering
    Article Snippet: .. Samples were observed and recorded using a Primovert inverted cell culture microscope (ZEISS, Jena, Germany) with Axiocam 208 color camera with bright-field imaging. ..

    Article Title: Establishment of an in vitro hairless guinea pig dermal model.
    Article Snippet: .. Cultures were imaged daily for 3 days on a Zeiss Primovert bright field microscope and viability was tracked during normal cell maintenance. .. HGP DF and Normal Human Dermal Fibroblasts (NHDF) (Lonza, CC-2511) were expanded for experiments comparing HDP DF to NHDF.

    Article Title: NK cells promote cardiac cell death and regulate myelopoiesis in myocardial infarction.
    Article Snippet: .. Nine days after their generation, the tissues were imaged at baseline using brightfield microscopy with a high-speed CCD camera (PLD672MU, Pixelink) mounted on Primovert microscope (Zeiss) at 10X magnification. ..

    Article Title: Establishment of an in vitro hairless guinea pig dermal model
    Article Snippet: .. Cultures were imaged daily for 3 days on a Zeiss Primovert bright field microscope and viability was tracked during normal cell maintenance. .. HGP DF and Normal Human Dermal Fibroblasts (NHDF) (Lonza, CC-2511) were expanded for experiments comparing HDP DF to NHDF.

    Article Title: Establishment of an in vitro hairless guinea pig dermal model
    Article Snippet: .. Brightfield images were captured on either a Keyence BZ-X800 in bright field or a Zeiss Primovert bright field microscope. .. Scale bars were added in Keyence software.

    Article Title: Establishment of an in vitro hairless guinea pig dermal model.
    Article Snippet: .. PLOS One | https://doi.org/10.1371/journal.pone.0344659 March 27, 2026 6 / 18 Brightfield images were captured on either a Keyence BZ-X800 in bright field or a Zeiss Primovert bright field microscope. .. Scale bars were added in Keyence software.

    Article Title: Immortalized Rat Tendon-Derived Stem Cells for Tendon Tissue Engineering
    Article Snippet: .. Samples were observed and recorded using a Primovert inverted cell culture microscope (ZEISS, Jena, Germany) with Axiocam 208 color camera with bright-field imaging. ..

    Imaging:

    Article Title: Immortalized Rat Tendon-Derived Stem Cells for Tendon Tissue Engineering
    Article Snippet: .. Samples were observed and recorded using a Primovert inverted cell culture microscope (ZEISS, Jena, Germany) with Axiocam 208 color camera with bright-field imaging. ..

    Article Title: Immortalized Rat Tendon-Derived Stem Cells for Tendon Tissue Engineering
    Article Snippet: .. Samples were observed and recorded using a Primovert inverted cell culture microscope (ZEISS, Jena, Germany) with Axiocam 208 color camera with bright-field imaging. ..

    Inverted Microscopy:

    Article Title: Protocol to enhance pre-sexual and sexual differentiation of Toxoplasma gondii using retinal cells and intestinal organoid-derived monolayers
    Article Snippet: 6 and 24-well plates , Corning , 3516 and 3524, respectively. .. Bright-field inverted microscope (20× 0.3 NA and 40× 0.8 NA objectives) , Zeiss , Primovert. .. 70 μm cell strainer , Corning , 431751.



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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