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cyflow space instrument  (Partec)

 
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    Structured Review

    Partec cyflow space instrument
    CWNPs characterization. ( A ) Representation of a CWNP obtained from A. infectoria mycelia cell wall, with negative zeta potential (mean ± SD) and approximately 200 nm diameter. ( B ) Image of ctCWNPs obtained using TEM (scale bar = 200 nm); the images obtained were used to observe the morphology and to quantify the diameter of the CWNPs. ( C ) Nanoparticles’ zeta potential, PDI, and area analyzed using Beckman Coulter DelsaTM Nano C Particle Analyser instrument; the diameter was quantified using TEM images. ( D ) Flow cytometry signatures of the CWNPs analyzed <t>on</t> <t>Partec</t> <t>Cyflow</t> with CWNPs labeled with fluorescein isothiocyanate (FITC). ctCWNPs, cell wall nanoparticles prepared from mycelia of A. infectoria grown under control conditions; casCWNPs, growth medium supplemented with caspofungin 1 µg/mL; nkCWNPs with nikkomycin Z 0.5 µg/mL; or pyrCWNPs, with pyroquilon 50 µg/mL.
    Cyflow Space Instrument, supplied by Partec, 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/result/cyflow space instrument/product/Partec
    Average 90 stars, based on 1 article reviews
    cyflow space instrument - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "Cell wall nanoparticles from hyphae of Alternaria infectoria grown with caspofungin, nikkomycin, or pyroquilon trigger different activation profiles in macrophages"

    Article Title: Cell wall nanoparticles from hyphae of Alternaria infectoria grown with caspofungin, nikkomycin, or pyroquilon trigger different activation profiles in macrophages

    Journal: Microbiology Spectrum

    doi: 10.1128/spectrum.00645-24

    CWNPs characterization. ( A ) Representation of a CWNP obtained from A. infectoria mycelia cell wall, with negative zeta potential (mean ± SD) and approximately 200 nm diameter. ( B ) Image of ctCWNPs obtained using TEM (scale bar = 200 nm); the images obtained were used to observe the morphology and to quantify the diameter of the CWNPs. ( C ) Nanoparticles’ zeta potential, PDI, and area analyzed using Beckman Coulter DelsaTM Nano C Particle Analyser instrument; the diameter was quantified using TEM images. ( D ) Flow cytometry signatures of the CWNPs analyzed on Partec Cyflow with CWNPs labeled with fluorescein isothiocyanate (FITC). ctCWNPs, cell wall nanoparticles prepared from mycelia of A. infectoria grown under control conditions; casCWNPs, growth medium supplemented with caspofungin 1 µg/mL; nkCWNPs with nikkomycin Z 0.5 µg/mL; or pyrCWNPs, with pyroquilon 50 µg/mL.
    Figure Legend Snippet: CWNPs characterization. ( A ) Representation of a CWNP obtained from A. infectoria mycelia cell wall, with negative zeta potential (mean ± SD) and approximately 200 nm diameter. ( B ) Image of ctCWNPs obtained using TEM (scale bar = 200 nm); the images obtained were used to observe the morphology and to quantify the diameter of the CWNPs. ( C ) Nanoparticles’ zeta potential, PDI, and area analyzed using Beckman Coulter DelsaTM Nano C Particle Analyser instrument; the diameter was quantified using TEM images. ( D ) Flow cytometry signatures of the CWNPs analyzed on Partec Cyflow with CWNPs labeled with fluorescein isothiocyanate (FITC). ctCWNPs, cell wall nanoparticles prepared from mycelia of A. infectoria grown under control conditions; casCWNPs, growth medium supplemented with caspofungin 1 µg/mL; nkCWNPs with nikkomycin Z 0.5 µg/mL; or pyrCWNPs, with pyroquilon 50 µg/mL.

    Techniques Used: Zeta Potential Analyzer, Flow Cytometry, Labeling, Control



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    CWNPs characterization. ( A ) Representation of a CWNP obtained from A. infectoria mycelia cell wall, with negative zeta potential (mean ± SD) and approximately 200 nm diameter. ( B ) Image of ctCWNPs obtained using TEM (scale bar = 200 nm); the images obtained were used to observe the morphology and to quantify the diameter of the CWNPs. ( C ) Nanoparticles’ zeta potential, PDI, and area analyzed using Beckman Coulter DelsaTM Nano C Particle Analyser instrument; the diameter was quantified using TEM images. ( D ) Flow cytometry signatures of the CWNPs analyzed <t>on</t> <t>Partec</t> <t>Cyflow</t> with CWNPs labeled with fluorescein isothiocyanate (FITC). ctCWNPs, cell wall nanoparticles prepared from mycelia of A. infectoria grown under control conditions; casCWNPs, growth medium supplemented with caspofungin 1 µg/mL; nkCWNPs with nikkomycin Z 0.5 µg/mL; or pyrCWNPs, with pyroquilon 50 µg/mL.
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    CWNPs characterization. ( A ) Representation of a CWNP obtained from A. infectoria mycelia cell wall, with negative zeta potential (mean ± SD) and approximately 200 nm diameter. ( B ) Image of ctCWNPs obtained using TEM (scale bar = 200 nm); the images obtained were used to observe the morphology and to quantify the diameter of the CWNPs. ( C ) Nanoparticles’ zeta potential, PDI, and area analyzed using Beckman Coulter DelsaTM Nano C Particle Analyser instrument; the diameter was quantified using TEM images. ( D ) Flow cytometry signatures of the CWNPs analyzed <t>on</t> <t>Partec</t> <t>Cyflow</t> with CWNPs labeled with fluorescein isothiocyanate (FITC). ctCWNPs, cell wall nanoparticles prepared from mycelia of A. infectoria grown under control conditions; casCWNPs, growth medium supplemented with caspofungin 1 µg/mL; nkCWNPs with nikkomycin Z 0.5 µg/mL; or pyrCWNPs, with pyroquilon 50 µg/mL.
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    CWNPs characterization. ( A ) Representation of a CWNP obtained from A. infectoria mycelia cell wall, with negative zeta potential (mean ± SD) and approximately 200 nm diameter. ( B ) Image of ctCWNPs obtained using TEM (scale bar = 200 nm); the images obtained were used to observe the morphology and to quantify the diameter of the CWNPs. ( C ) Nanoparticles’ zeta potential, PDI, and area analyzed using Beckman Coulter DelsaTM Nano C Particle Analyser instrument; the diameter was quantified using TEM images. ( D ) Flow cytometry signatures of the CWNPs analyzed <t>on</t> <t>Partec</t> <t>Cyflow</t> with CWNPs labeled with fluorescein isothiocyanate (FITC). ctCWNPs, cell wall nanoparticles prepared from mycelia of A. infectoria grown under control conditions; casCWNPs, growth medium supplemented with caspofungin 1 µg/mL; nkCWNPs with nikkomycin Z 0.5 µg/mL; or pyrCWNPs, with pyroquilon 50 µg/mL.
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    CWNPs characterization. ( A ) Representation of a CWNP obtained from A. infectoria mycelia cell wall, with negative zeta potential (mean ± SD) and approximately 200 nm diameter. ( B ) Image of ctCWNPs obtained using TEM (scale bar = 200 nm); the images obtained were used to observe the morphology and to quantify the diameter of the CWNPs. ( C ) Nanoparticles’ zeta potential, PDI, and area analyzed using Beckman Coulter DelsaTM Nano C Particle Analyser instrument; the diameter was quantified using TEM images. ( D ) Flow cytometry signatures of the CWNPs analyzed <t>on</t> <t>Partec</t> <t>Cyflow</t> with CWNPs labeled with fluorescein isothiocyanate (FITC). ctCWNPs, cell wall nanoparticles prepared from mycelia of A. infectoria grown under control conditions; casCWNPs, growth medium supplemented with caspofungin 1 µg/mL; nkCWNPs with nikkomycin Z 0.5 µg/mL; or pyrCWNPs, with pyroquilon 50 µg/mL.
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    Image Search Results


    CWNPs characterization. ( A ) Representation of a CWNP obtained from A. infectoria mycelia cell wall, with negative zeta potential (mean ± SD) and approximately 200 nm diameter. ( B ) Image of ctCWNPs obtained using TEM (scale bar = 200 nm); the images obtained were used to observe the morphology and to quantify the diameter of the CWNPs. ( C ) Nanoparticles’ zeta potential, PDI, and area analyzed using Beckman Coulter DelsaTM Nano C Particle Analyser instrument; the diameter was quantified using TEM images. ( D ) Flow cytometry signatures of the CWNPs analyzed on Partec Cyflow with CWNPs labeled with fluorescein isothiocyanate (FITC). ctCWNPs, cell wall nanoparticles prepared from mycelia of A. infectoria grown under control conditions; casCWNPs, growth medium supplemented with caspofungin 1 µg/mL; nkCWNPs with nikkomycin Z 0.5 µg/mL; or pyrCWNPs, with pyroquilon 50 µg/mL.

    Journal: Microbiology Spectrum

    Article Title: Cell wall nanoparticles from hyphae of Alternaria infectoria grown with caspofungin, nikkomycin, or pyroquilon trigger different activation profiles in macrophages

    doi: 10.1128/spectrum.00645-24

    Figure Lengend Snippet: CWNPs characterization. ( A ) Representation of a CWNP obtained from A. infectoria mycelia cell wall, with negative zeta potential (mean ± SD) and approximately 200 nm diameter. ( B ) Image of ctCWNPs obtained using TEM (scale bar = 200 nm); the images obtained were used to observe the morphology and to quantify the diameter of the CWNPs. ( C ) Nanoparticles’ zeta potential, PDI, and area analyzed using Beckman Coulter DelsaTM Nano C Particle Analyser instrument; the diameter was quantified using TEM images. ( D ) Flow cytometry signatures of the CWNPs analyzed on Partec Cyflow with CWNPs labeled with fluorescein isothiocyanate (FITC). ctCWNPs, cell wall nanoparticles prepared from mycelia of A. infectoria grown under control conditions; casCWNPs, growth medium supplemented with caspofungin 1 µg/mL; nkCWNPs with nikkomycin Z 0.5 µg/mL; or pyrCWNPs, with pyroquilon 50 µg/mL.

    Article Snippet: It was performed on Partec CyFlow space instrument.

    Techniques: Zeta Potential Analyzer, Flow Cytometry, Labeling, Control