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zeta view basic nta (nanoparticle tracking video microscope  (Particle Metrix)

 
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    Particle Metrix zeta view basic nta (nanoparticle tracking video microscope
    Zeta View Basic Nta (Nanoparticle Tracking Video Microscope, 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/result/zeta view basic nta (nanoparticle tracking video microscope/product/Particle Metrix
    Average 90 stars, based on 1 article reviews
    zeta view basic nta (nanoparticle tracking video microscope - by Bioz Stars, 2026-05
    90/100 stars

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    Zeta View Basic Nta (Nanoparticle Tracking Video Microscope, 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
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    ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) <t>ZetaView</t> analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.
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    ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) <t>ZetaView</t> analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.
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    ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) <t>ZetaView</t> analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.
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    ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) <t>ZetaView</t> analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.
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    ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) <t>ZetaView</t> analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.
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    ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) <t>ZetaView</t> analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.
    Zetaview® Basic Nta – Nanoparticle Tracking Video Microscope 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
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    zetaview nanoparticle tracking analysis basic nta-nanoparticle tracking video microscope pmx-120  (Particle Metrix)
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    ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) <t>ZetaView</t> analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.
    Zetaview Nanoparticle Tracking Analysis Basic Nta Nanoparticle Tracking Video Microscope 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
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    nanoparticle tracking video microscope pmx-120  (Particle Metrix)
    90
    Particle Metrix nanoparticle tracking video microscope pmx-120
    ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) <t>ZetaView</t> analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.
    Nanoparticle Tracking Video Microscope 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/result/nanoparticle tracking video microscope pmx-120/product/Particle Metrix
    Average 90 stars, based on 1 article reviews
    nanoparticle tracking video microscope pmx-120 - by Bioz Stars, 2026-05
    90/100 stars
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    ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) ZetaView analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.

    Journal: Science Advances

    Article Title: Blood-derived APLP1 + extracellular vesicles are potential biomarkers for the early diagnosis of brain diseases

    doi: 10.1126/sciadv.ado6894

    Figure Lengend Snippet: ( A ) NTA-derived graphs showing size and concentration metrics of the brain tissue EVs. ( B ) Percentage-based size distributions of EVs, derived from the data presented in (A). ( C ) TEM images, at ×10,000 and ×20,000 magnifications, depicting EV morphology. Scale bars, 100 nm. Error bars in the figures delineate the SE of the mean (±SEM) from triplicate measurements of brain tissue EVs. ( D ) Western blot of APLP1 and EV markers in brain tissues and brain tissue EVs from five C57BL/6 mice. ( E ) ZetaView analysis of plasma-derived EVs in WT and Thy-1 GFP M line mice. Total EVs appear in light-scatter mode, GFP + EVs in 488-nm fluorescence mode, and APLP1 + EVs in 640-nm fluorescence mode. ( F and G ) EV size distribution in WT and Thy-1 GFP M line mice using ZetaView. ( H ) Average EV size ranges between 198 and 217.8 nm in both mouse types. ( I ) Immunostaining of APLP1 in plasma EVs from Thy-1 GFP M line mice, with white arrowheads highlighting APLP1 + GFP + EVs. Scale bars, 25 μm. All data were obtained from at least three mice.

    Article Snippet: EVs were diluted in PBS (1-ml final volume) and examined under a ZetaView Nanoparticle Tracking Video Microscope (Particle Metrix, Inning, Germany).

    Techniques: Derivative Assay, Concentration Assay, Western Blot, Clinical Proteomics, Fluorescence, Immunostaining