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multiple—laser zetaview ® f-nta nanoparticle tracking analyzers system  (Particle Metrix)

 
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    Structured Review

    Particle Metrix multiple—laser zetaview ® f-nta nanoparticle tracking analyzers system
    Extracellular vesicles (EVs) were isolated from horse bronchoalveolar lavage fluid (BALF) (n = 3 horses) following sample processing via centrifugation (gray boxes in “Sample Processing” panel) using four different EV isolation methods, resulting in a total of 12 samples. EVs were evaluated and characterized through <t>nanoparticle</t> tracking analysis (NTA), micro bicinchoninic acid (microBCA) protein assay, proteomics, and transmission electron microscopy (TEM). Figure created with biorender.com.
    Multiple—Laser Zetaview ® F Nta Nanoparticle Tracking Analyzers System, supplied by Particle Metrix, 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/zetaview+f-nta+nanoparticle+tracking+analyzer/pmc11760557-81-14-22?v=Particle+Metrix
    Average 90 stars, based on 1 article reviews
    multiple—laser zetaview ® f-nta nanoparticle tracking analyzers system - by Bioz Stars, 2026-08
    90/100 stars

    Images

    1) Product Images from "Respiratory extracellular vesicle isolation optimization through proteomic profiling of equine samples and identification of candidates for cell-of-origin studies"

    Article Title: Respiratory extracellular vesicle isolation optimization through proteomic profiling of equine samples and identification of candidates for cell-of-origin studies

    Journal: PLOS ONE

    doi: 10.1371/journal.pone.0315743

    Extracellular vesicles (EVs) were isolated from horse bronchoalveolar lavage fluid (BALF) (n = 3 horses) following sample processing via centrifugation (gray boxes in “Sample Processing” panel) using four different EV isolation methods, resulting in a total of 12 samples. EVs were evaluated and characterized through nanoparticle tracking analysis (NTA), micro bicinchoninic acid (microBCA) protein assay, proteomics, and transmission electron microscopy (TEM). Figure created with biorender.com.
    Figure Legend Snippet: Extracellular vesicles (EVs) were isolated from horse bronchoalveolar lavage fluid (BALF) (n = 3 horses) following sample processing via centrifugation (gray boxes in “Sample Processing” panel) using four different EV isolation methods, resulting in a total of 12 samples. EVs were evaluated and characterized through nanoparticle tracking analysis (NTA), micro bicinchoninic acid (microBCA) protein assay, proteomics, and transmission electron microscopy (TEM). Figure created with biorender.com.

    Techniques Used: Isolation, Centrifugation, Transmission Assay, Electron Microscopy



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    Particle Metrix multiple—laser zetaview ® f-nta nanoparticle tracking analyzers system
    Extracellular vesicles (EVs) were isolated from horse bronchoalveolar lavage fluid (BALF) (n = 3 horses) following sample processing via centrifugation (gray boxes in “Sample Processing” panel) using four different EV isolation methods, resulting in a total of 12 samples. EVs were evaluated and characterized through <t>nanoparticle</t> tracking analysis (NTA), micro bicinchoninic acid (microBCA) protein assay, proteomics, and transmission electron microscopy (TEM). Figure created with biorender.com.
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    Extracellular vesicles (EVs) were isolated from horse bronchoalveolar lavage fluid (BALF) (n = 3 horses) following sample processing via centrifugation (gray boxes in “Sample Processing” panel) using four different EV isolation methods, resulting in a total of 12 samples. EVs were evaluated and characterized through <t>nanoparticle</t> tracking analysis (NTA), micro bicinchoninic acid (microBCA) protein assay, proteomics, and transmission electron microscopy (TEM). Figure created with biorender.com.
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    Extracellular vesicles (EVs) were isolated from horse bronchoalveolar lavage fluid (BALF) (n = 3 horses) following sample processing via centrifugation (gray boxes in “Sample Processing” panel) using four different EV isolation methods, resulting in a total of 12 samples. EVs were evaluated and characterized through <t>nanoparticle</t> tracking analysis (NTA), micro bicinchoninic acid (microBCA) protein assay, proteomics, and transmission electron microscopy (TEM). Figure created with biorender.com.
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    Particle Metrix multiple-laser zetaview® f-nta nanoparticle tracking analyzers

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    Particle Metrix multiple-laser zetaview ® f-nta nanoparticle tracking analyzers
    Isolation and characterization of serum exosomes. (A) Schematic representation of serum exosomes (Con-exo) isolated from rats. (B) Con-exo was photographed by transmission electron microscopy (TEM). Scale bar = 50 nm. (C) Representative immunoblotting images of exosomal markers such as CD9 and TSG101 in Con-exo. (D) Particle size of Con-exo was measured by <t>nanoparticle</t> tracing analysis.
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    Image Search Results


    Extracellular vesicles (EVs) were isolated from horse bronchoalveolar lavage fluid (BALF) (n = 3 horses) following sample processing via centrifugation (gray boxes in “Sample Processing” panel) using four different EV isolation methods, resulting in a total of 12 samples. EVs were evaluated and characterized through nanoparticle tracking analysis (NTA), micro bicinchoninic acid (microBCA) protein assay, proteomics, and transmission electron microscopy (TEM). Figure created with biorender.com.

    Journal: PLOS ONE

    Article Title: Respiratory extracellular vesicle isolation optimization through proteomic profiling of equine samples and identification of candidates for cell-of-origin studies

    doi: 10.1371/journal.pone.0315743

    Figure Lengend Snippet: Extracellular vesicles (EVs) were isolated from horse bronchoalveolar lavage fluid (BALF) (n = 3 horses) following sample processing via centrifugation (gray boxes in “Sample Processing” panel) using four different EV isolation methods, resulting in a total of 12 samples. EVs were evaluated and characterized through nanoparticle tracking analysis (NTA), micro bicinchoninic acid (microBCA) protein assay, proteomics, and transmission electron microscopy (TEM). Figure created with biorender.com.

    Article Snippet: EV samples from N = 3 horses per isolation method were evaluated using the Multiple—Laser ZetaView ® f-NTA Nanoparticle Tracking Analyzers System (Particle Metrix), including nine fractions per horse for each of the two size exclusion chromatography columns.

    Techniques: Isolation, Centrifugation, Transmission Assay, Electron Microscopy

    Journal: bioRxiv

    Article Title: Effect of homotypic vs . heterotypic interactions on the cellular uptake of extracellular vesicles

    doi: 10.1101/2023.10.23.563628

    Figure Lengend Snippet:

    Article Snippet: EV particle concentrations were determined on a multiple-laser ZetaView f-NTA Nanoparticle Tracking Analyzer (Particle Metrix Inc., Mebane, NC).

    Techniques: Concentration Assay, Standard Deviation

    Isolation and characterization of serum exosomes. (A) Schematic representation of serum exosomes (Con-exo) isolated from rats. (B) Con-exo was photographed by transmission electron microscopy (TEM). Scale bar = 50 nm. (C) Representative immunoblotting images of exosomal markers such as CD9 and TSG101 in Con-exo. (D) Particle size of Con-exo was measured by nanoparticle tracing analysis.

    Journal: Frontiers in Cellular Neuroscience

    Article Title: Healthy Serum-Derived Exosomes Improve Neurological Outcomes and Protect Blood–Brain Barrier by Inhibiting Endothelial Cell Apoptosis and Reversing Autophagy-Mediated Tight Junction Protein Reduction in Rat Stroke Model

    doi: 10.3389/fncel.2022.841544

    Figure Lengend Snippet: Isolation and characterization of serum exosomes. (A) Schematic representation of serum exosomes (Con-exo) isolated from rats. (B) Con-exo was photographed by transmission electron microscopy (TEM). Scale bar = 50 nm. (C) Representative immunoblotting images of exosomal markers such as CD9 and TSG101 in Con-exo. (D) Particle size of Con-exo was measured by nanoparticle tracing analysis.

    Article Snippet: The size and concentration distribution profile of serum exosomes were analyzed using a Multiple-Laser ZetaView ® f-NTA Nanoparticle Tracking Analyzers (Particle Metrix, Germany).

    Techniques: Isolation, Transmission Assay, Electron Microscopy, Western Blot