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multi channel scanning inverted fluorescence microscope  (Danaher Inc)


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    Danaher Inc multi channel scanning inverted fluorescence microscope
    Preparation and characterization of Lip-Exo/Pae. (A) <t>Fluorescence</t> inverted <t>microscope</t> pictures of liposome-exosome fusion (liposomes in red, exosomes in green, Lip-Exo/Pae in yellow). (B) Schematic diagram of liposome and exosome fusion. (C) Appearance of Lip-Exo/Pae solution. (D) Tyndall effect of Lip-Exo/Pae colloidal solution. (E) TEM Image of Lip-Exo/Pae. TEM Image of Lip-Exo/Pae. Scale bars represent 200 nm. (F) Particle size distribution map of Lip-Exo/Pae. (G) Zeta potential and PDI of Lip-Exo/Pae. (H) In vitro dialysis release curves of each formulation group. (I) The release curves were fitted to each formulation group using the Weibull mathematical model. (J) ABTS clearance results for each group of formulations at varying concentrations. (K) The scavenging results of hydroxyl radicals by different concentrations of each formulation group. (L) Blood compatibility test results of Lip-Exo/Pae. (M) Cell viability after 24-h incubation of HT22 cells with varying concentrations of Lip-Exo/Pae. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Multi Channel Scanning Inverted Fluorescence Microscope, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 8052 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/multi+channel+scanning+inverted+fluorescence+microscope/pmc12914197-106-21-28?v=Danaher+Inc
    Average 99 stars, based on 8052 article reviews
    multi channel scanning inverted fluorescence microscope - by Bioz Stars, 2026-08
    99/100 stars

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    1) Product Images from "Bionic design based on liposome-exosome hybrid nanoparticles for synergistic delivery of paeonol to achieve neuroprotection and improvement of motor function in Parkinson's disease model mice"

    Article Title: Bionic design based on liposome-exosome hybrid nanoparticles for synergistic delivery of paeonol to achieve neuroprotection and improvement of motor function in Parkinson's disease model mice

    Journal: Materials Today Bio

    doi: 10.1016/j.mtbio.2026.102847

    Preparation and characterization of Lip-Exo/Pae. (A) Fluorescence inverted microscope pictures of liposome-exosome fusion (liposomes in red, exosomes in green, Lip-Exo/Pae in yellow). (B) Schematic diagram of liposome and exosome fusion. (C) Appearance of Lip-Exo/Pae solution. (D) Tyndall effect of Lip-Exo/Pae colloidal solution. (E) TEM Image of Lip-Exo/Pae. TEM Image of Lip-Exo/Pae. Scale bars represent 200 nm. (F) Particle size distribution map of Lip-Exo/Pae. (G) Zeta potential and PDI of Lip-Exo/Pae. (H) In vitro dialysis release curves of each formulation group. (I) The release curves were fitted to each formulation group using the Weibull mathematical model. (J) ABTS clearance results for each group of formulations at varying concentrations. (K) The scavenging results of hydroxyl radicals by different concentrations of each formulation group. (L) Blood compatibility test results of Lip-Exo/Pae. (M) Cell viability after 24-h incubation of HT22 cells with varying concentrations of Lip-Exo/Pae. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Figure Legend Snippet: Preparation and characterization of Lip-Exo/Pae. (A) Fluorescence inverted microscope pictures of liposome-exosome fusion (liposomes in red, exosomes in green, Lip-Exo/Pae in yellow). (B) Schematic diagram of liposome and exosome fusion. (C) Appearance of Lip-Exo/Pae solution. (D) Tyndall effect of Lip-Exo/Pae colloidal solution. (E) TEM Image of Lip-Exo/Pae. TEM Image of Lip-Exo/Pae. Scale bars represent 200 nm. (F) Particle size distribution map of Lip-Exo/Pae. (G) Zeta potential and PDI of Lip-Exo/Pae. (H) In vitro dialysis release curves of each formulation group. (I) The release curves were fitted to each formulation group using the Weibull mathematical model. (J) ABTS clearance results for each group of formulations at varying concentrations. (K) The scavenging results of hydroxyl radicals by different concentrations of each formulation group. (L) Blood compatibility test results of Lip-Exo/Pae. (M) Cell viability after 24-h incubation of HT22 cells with varying concentrations of Lip-Exo/Pae. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Techniques Used: Fluorescence, Inverted Microscopy, Liposomes, Zeta Potential Analyzer, In Vitro, Formulation, Incubation



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    multi channel scanning inverted fluorescence microscope  (Danaher Inc)
    99
    Danaher Inc multi channel scanning inverted fluorescence microscope
    Preparation and characterization of Lip-Exo/Pae. (A) <t>Fluorescence</t> inverted <t>microscope</t> pictures of liposome-exosome fusion (liposomes in red, exosomes in green, Lip-Exo/Pae in yellow). (B) Schematic diagram of liposome and exosome fusion. (C) Appearance of Lip-Exo/Pae solution. (D) Tyndall effect of Lip-Exo/Pae colloidal solution. (E) TEM Image of Lip-Exo/Pae. TEM Image of Lip-Exo/Pae. Scale bars represent 200 nm. (F) Particle size distribution map of Lip-Exo/Pae. (G) Zeta potential and PDI of Lip-Exo/Pae. (H) In vitro dialysis release curves of each formulation group. (I) The release curves were fitted to each formulation group using the Weibull mathematical model. (J) ABTS clearance results for each group of formulations at varying concentrations. (K) The scavenging results of hydroxyl radicals by different concentrations of each formulation group. (L) Blood compatibility test results of Lip-Exo/Pae. (M) Cell viability after 24-h incubation of HT22 cells with varying concentrations of Lip-Exo/Pae. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Multi Channel Scanning Inverted Fluorescence Microscope, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/multi+channel+scanning+inverted+fluorescence+microscope/pmc12914197-106-21-28?v=Danaher+Inc
    Average 99 stars, based on 1 article reviews
    multi channel scanning inverted fluorescence microscope - by Bioz Stars, 2026-08
    99/100 stars
    		  Buy from Supplier

    Image Search Results


    Preparation and characterization of Lip-Exo/Pae. (A) Fluorescence inverted microscope pictures of liposome-exosome fusion (liposomes in red, exosomes in green, Lip-Exo/Pae in yellow). (B) Schematic diagram of liposome and exosome fusion. (C) Appearance of Lip-Exo/Pae solution. (D) Tyndall effect of Lip-Exo/Pae colloidal solution. (E) TEM Image of Lip-Exo/Pae. TEM Image of Lip-Exo/Pae. Scale bars represent 200 nm. (F) Particle size distribution map of Lip-Exo/Pae. (G) Zeta potential and PDI of Lip-Exo/Pae. (H) In vitro dialysis release curves of each formulation group. (I) The release curves were fitted to each formulation group using the Weibull mathematical model. (J) ABTS clearance results for each group of formulations at varying concentrations. (K) The scavenging results of hydroxyl radicals by different concentrations of each formulation group. (L) Blood compatibility test results of Lip-Exo/Pae. (M) Cell viability after 24-h incubation of HT22 cells with varying concentrations of Lip-Exo/Pae. (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: Bionic design based on liposome-exosome hybrid nanoparticles for synergistic delivery of paeonol to achieve neuroprotection and improvement of motor function in Parkinson's disease model mice

    doi: 10.1016/j.mtbio.2026.102847

    Figure Lengend Snippet: Preparation and characterization of Lip-Exo/Pae. (A) Fluorescence inverted microscope pictures of liposome-exosome fusion (liposomes in red, exosomes in green, Lip-Exo/Pae in yellow). (B) Schematic diagram of liposome and exosome fusion. (C) Appearance of Lip-Exo/Pae solution. (D) Tyndall effect of Lip-Exo/Pae colloidal solution. (E) TEM Image of Lip-Exo/Pae. TEM Image of Lip-Exo/Pae. Scale bars represent 200 nm. (F) Particle size distribution map of Lip-Exo/Pae. (G) Zeta potential and PDI of Lip-Exo/Pae. (H) In vitro dialysis release curves of each formulation group. (I) The release curves were fitted to each formulation group using the Weibull mathematical model. (J) ABTS clearance results for each group of formulations at varying concentrations. (K) The scavenging results of hydroxyl radicals by different concentrations of each formulation group. (L) Blood compatibility test results of Lip-Exo/Pae. (M) Cell viability after 24-h incubation of HT22 cells with varying concentrations of Lip-Exo/Pae. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Finally, 10 μL Lip-Exo/Pae samples prepared using both methods were mounted on microscope slides, and fluorescence colocalization was assessed using a multi-channel scanning inverted fluorescence microscope (DMI 8, Leica, Germany) to determine membrane fusion.

    Techniques: Fluorescence, Inverted Microscopy, Liposomes, Zeta Potential Analyzer, In Vitro, Formulation, Incubation