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zetaview nanoparticle tracking analyzer pmx-120  (Particle Metrix)

 
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    Particle Metrix zetaview nanoparticle tracking analyzer pmx-120
    Zetaview Nanoparticle Tracking Analyzer Pmx 120, 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+nanoparticle+tracking+analyzer+pmx-120/zetaview+pmx+110/pmc12183344-61-11-16
    Average 90 stars, based on 1 article reviews
    zetaview nanoparticle tracking analyzer pmx-120 - by Bioz Stars, 2026-10
    90/100 stars

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    other:

    Article Title: Multifaceted action of stem cell-derived extracellular vesicles for nonalcoholic steatohepatitis.
    Article Snippet: Nonalcoholic steatohepatitis (NASH) is a chronic liver disease associated with metabolic syndrome.. Extracellular vesicles (EVs) are essential signaling mediators containing functional biomolecules.. EVs are secreted from various cell types, and recent studies have shown that mesenchymal stem cell-derived EVs have therapeutic potential against immune and metabolic diseases.

    Article Title: Pan PPAR agonist stimulation of induced MSCs produces extracellular vesicles with enhanced renoprotective effect for acute kidney injury.
    Article Snippet: Measurements of the particle size distribution and concentration of iMSC-EVs and pan PPAR-iMSC-EVs were performed using a ZetaView Nanoparticle Tracking Analyzer PMX-120 instrument (Particle Metrix, Inning am Ammersee, Germany).

    Article Title: Extracellular Vesicles from Induced Mesenchymal Stem Cells Inhibit Acute Kidney Injury to Chronic Kidney Disease Transition.
    Article Snippet: The particle size distribution and concentration of iMSC-EVs were measured using a ZetaView Nanoparticle Tracking Analyzer PMX-120 instrument (Particle Metrix).

    Article Title: iMSC-Derived Extracellular Vesicles Improve Atopic Dermatitis by Augmenting Skin Barrier Integrity and Inhibiting Inflammation, Pruritus and Th2 Immune Responses.
    Article Snippet: Particle size distribution and concentration of IFN-γ-iMSC-EVs were assessed using the ZetaView Nanoparticle Tracking Analyzer PMX-120 (Particle Metrix, Inning amAmmersee, Germany) based on NTA.

    Article Title: iMSC‐Derived Extracellular Vesicles Improve Atopic Dermatitis by Augmenting Skin Barrier Integrity and Inhibiting Inflammation, Pruritus and Th2 Immune Responses
    Article Snippet: Particle size distribution and concentration of IFN‐γ‐iMSC‐EVs were assessed using the ZetaView Nanoparticle Tracking Analyzer PMX‐120 (Particle Metrix, Inning am Ammersee, Germany) based on NTA.

    Article Title: Extracellular vesicles from IFN-γ-primed mesenchymal stem cells repress atopic dermatitis in mice
    Article Snippet: Measurements of particle size distribution and concentration of IFN-γ-iMSC-EVs were performed using the ZetaView Nanoparticle Tracking Analyzer PMX-120 instrument (Particle Metrix, Inning am Ammersee, Germany) based on NTA.

    Article Title: Extracellular vesicles from induced pluripotent stem cell-derived mesenchymal stem cells enhance the recovery of acute kidney injury.
    Article Snippet: Background aims: To investigate whether the extracellular vesicles (EVs) from mesenchymal stem cell like cells derived from induced pluripotent stem cells (iMSC-EVs) can inhibit the progression of acute kidney injury (AKI).. Methods: The characteristics of iMSC-EVs were confirmed by immunoblotting, cryo-transmission electron microscopy, nanoparticle tracking analysis, and their localization in kidneys.. Using human renal epithelial cells, the potential of iMSC-EVs to stimulate the growth and survival of HK-2 cells undergoing cisplatininduced cell death was investigated.

    Concentration Assay:

    Article Title: Large‐scale heparin‐based bind‐and‐elute chromatography identifies two biologically distinct populations of extracellular vesicles
    Article Snippet: The membranes were imaged using a Li‐Cor Odyssey Imager (Li‐Cor 9120). .. ZetaView Nanoparticle Tracking Analyzer (Particle Metrix, PMX‐120) was used to determine particle concentration, size distribution, and zeta potential. .. The instrument was standardized using 100 nm Nanosphere beads (Thermo Scientific 3100A) per system requirement at the sensitivity of 65 and shutter of 100 (ZetaView 8.04.02).

    Zeta Potential Analyzer:

    Article Title: Large‐scale heparin‐based bind‐and‐elute chromatography identifies two biologically distinct populations of extracellular vesicles
    Article Snippet: The membranes were imaged using a Li‐Cor Odyssey Imager (Li‐Cor 9120). .. ZetaView Nanoparticle Tracking Analyzer (Particle Metrix, PMX‐120) was used to determine particle concentration, size distribution, and zeta potential. .. The instrument was standardized using 100 nm Nanosphere beads (Thermo Scientific 3100A) per system requirement at the sensitivity of 65 and shutter of 100 (ZetaView 8.04.02).



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    Characterization of E. coli Ag43 −ve and Ag43 +ve MVs. MVs isolated from ( A ) E. coli HEHA16 pBAD/MycHisA (Ag43 −ve ) and ( B ) E. coli HEHA16 pBAD/MycHisA:: agn43 (Ag43 +ve ) were visualized by transmission electron microscopy. Scale bar = 100 nm. Images are representative of three biological replicates. ( C ) The number of Ag43 −ve and Ag43 +ve MVs produced per 10 10 bacterial cells was determined by ZetaView <t>Nanoparticle</t> Tracking Analysis (NTA). Data are represented as the mean ± SEM of three biological replicates. * P < 0.05, unpaired t -test. ( D ) The number of viable Ag43 −ve and Ag43 +ve E. coli HEHA16 bacteria present in individual cultures from which MVs were isolated was determined by viable counts. Data show CFU/mL of individual cultures, and the mean ± SEM of three biological replicates. ns, not significant. ( E ) The size distribution of Ag43 −ve MVs and Ag43 +ve MVs was determined using ZetaView NTA. Data represent the mean of three biological replicates. ( F ) Quantification of the size distribution of Ag43 −ve MVs (squares; open bars) or Ag43 +ve MVs (circles; grey bars) by ZetaView NTA. Data are represented as the mean ± SEM of three biological replicates. * P < 0.05, unpaired t -test within each size range.
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    Characterization of E. coli Ag43 −ve and Ag43 +ve MVs. MVs isolated from ( A ) E. coli HEHA16 pBAD/MycHisA (Ag43 −ve ) and ( B ) E. coli HEHA16 pBAD/MycHisA:: agn43 (Ag43 +ve ) were visualized by transmission electron microscopy. Scale bar = 100 nm. Images are representative of three biological replicates. ( C ) The number of Ag43 −ve and Ag43 +ve MVs produced per 10 10 bacterial cells was determined by ZetaView Nanoparticle Tracking Analysis (NTA). Data are represented as the mean ± SEM of three biological replicates. * P < 0.05, unpaired t -test. ( D ) The number of viable Ag43 −ve and Ag43 +ve E. coli HEHA16 bacteria present in individual cultures from which MVs were isolated was determined by viable counts. Data show CFU/mL of individual cultures, and the mean ± SEM of three biological replicates. ns, not significant. ( E ) The size distribution of Ag43 −ve MVs and Ag43 +ve MVs was determined using ZetaView NTA. Data represent the mean of three biological replicates. ( F ) Quantification of the size distribution of Ag43 −ve MVs (squares; open bars) or Ag43 +ve MVs (circles; grey bars) by ZetaView NTA. Data are represented as the mean ± SEM of three biological replicates. * P < 0.05, unpaired t -test within each size range.

    Journal: Microbiology Spectrum

    Article Title: Antigen 43 associated with Escherichia coli membrane vesicles contributes to bacterial cell association and biofilm formation

    doi: 10.1128/spectrum.01890-24

    Figure Lengend Snippet: Characterization of E. coli Ag43 −ve and Ag43 +ve MVs. MVs isolated from ( A ) E. coli HEHA16 pBAD/MycHisA (Ag43 −ve ) and ( B ) E. coli HEHA16 pBAD/MycHisA:: agn43 (Ag43 +ve ) were visualized by transmission electron microscopy. Scale bar = 100 nm. Images are representative of three biological replicates. ( C ) The number of Ag43 −ve and Ag43 +ve MVs produced per 10 10 bacterial cells was determined by ZetaView Nanoparticle Tracking Analysis (NTA). Data are represented as the mean ± SEM of three biological replicates. * P < 0.05, unpaired t -test. ( D ) The number of viable Ag43 −ve and Ag43 +ve E. coli HEHA16 bacteria present in individual cultures from which MVs were isolated was determined by viable counts. Data show CFU/mL of individual cultures, and the mean ± SEM of three biological replicates. ns, not significant. ( E ) The size distribution of Ag43 −ve MVs and Ag43 +ve MVs was determined using ZetaView NTA. Data represent the mean of three biological replicates. ( F ) Quantification of the size distribution of Ag43 −ve MVs (squares; open bars) or Ag43 +ve MVs (circles; grey bars) by ZetaView NTA. Data are represented as the mean ± SEM of three biological replicates. * P < 0.05, unpaired t -test within each size range.

    Article Snippet: MV size and concentration were determined using the nanoparticle tracking analyzer ZetaView basic PMX-120 NTA (Particle Metrix, Germany), as previously ( ).

    Techniques: Isolation, Transmission Assay, Electron Microscopy, Produced, Bacteria