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tem  (Hitachi Ltd)


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    Hitachi Ltd tem
    Tem, supplied by Hitachi Ltd, used in various techniques. Bioz Stars score: 99/100, based on 45403 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/tem/product/Hitachi Ltd
    Average 99 stars, based on 45403 article reviews
    tem - by Bioz Stars, 2026-05
    99/100 stars

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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Image Search Results


    Characterization of CAMs. (a) TEM images of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.

    Journal: Bioactive Materials

    Article Title: Artificial mitochondria ameliorates osteoarthritis through restoring cellular energy metabolism homeostasis

    doi: 10.1016/j.bioactmat.2026.02.028

    Figure Lengend Snippet: Characterization of CAMs. (a) TEM images of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.

    Article Snippet: The TEM images of the samples were captured using a JEOL JEM-2100 transmission electron microscope.

    Techniques: Control, Zeta Potential Analyzer