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transmission electron microscope tem images  (JEOL)
99
JEOL transmission electron microscope tem images
Transmission Electron Microscope Tem Images, supplied by JEOL, 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/microscope+images/JEM-1400Flash+Transmission+Electron+Microscope/pm41747576-210-0-11
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transmission electron microscope tem images - by Bioz Stars, 2026-09
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tem images  (JEOL)
99
JEOL tem images
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.
Tem Images, supplied by JEOL, 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/microscope+images/JEM-2100+Transmission+Electron+Microscope/pmc12972744-522-1-10
Average 99 stars, based on 1 article reviews
tem images - by Bioz Stars, 2026-09
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scanning electron microscopy sem imaging  (JEOL)
99
JEOL scanning electron microscopy sem imaging
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.
Scanning Electron Microscopy Sem Imaging, supplied by JEOL, 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/microscope+images/JSM-7800F+Scanning+Electron+Microscope/pmc12964231-104-0-9
Average 99 stars, based on 1 article reviews
scanning electron microscopy sem imaging - by Bioz Stars, 2026-09
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atomic force microscope afm images  (Veeco)
86
Veeco atomic force microscope afm images
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.
Atomic Force Microscope Afm Images, supplied by Veeco, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/microscope+images/atomic+force+microscopy/pmc13282994-57-0-15
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atomic force microscope afm images - by Bioz Stars, 2026-09
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eclipse ti2 high content imaging microscope  (Nikon)
99
Nikon eclipse ti2 high content imaging microscope
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.
Eclipse Ti2 High Content Imaging Microscope, supplied by Nikon, 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/microscope+images/ECLIPSE+Ti2/pmc12887268-306-7-6
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eclipse ti2 high content imaging microscope - by Bioz Stars, 2026-09
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scanning electron microscope sem images  (JEOL)
99
JEOL scanning electron microscope sem images
Synthesis and characterization of aCD47-CATE nanoplatform. (A) The preparation of aCD47-CATE nanoplatform. (B) UV-Vis absorption spectra of Croc under different pH. (C) The morphology of the aCD47-CATE nanostructure as visualized by transmission electron microscopy (TEM), scale bar = 100 nm (up) and scanning electron <t>microscope</t> <t>(SEM),</t> scale bar = 200 nm (down). (D) Changes in the zeta potential that occurred during the synthesis steps for both CATE and aCD47-CATE nanoplatform. Data are presented as mean ± SD (n = 3). (E) A characteristic high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) micrograph, presented alongside the associated elemental distribution maps for the aCD47-CATE nanoplatform. (F) NIR-II thermal images of the aCD47-CATE nanoplatform in a phantom under 1064 nm laser irradiation at different power densities (0.5, 1.0, 1.5, 2.0 W/cm 2 ) for 360 s. (G) Graphs depicting the temperature rise for the aCD47-CATE NPs under different laser power at 1064 nm laser irradiation. (H) Multiple heating cycles of aCD47-CATE nanoplatform under 1.0 W/cm 2 at 1064 nm laser irradiation.
Scanning Electron Microscope Sem Images, supplied by JEOL, 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/microscope+images/JEM-2100+Transmission+Electron+Microscope/pmc13054091-276-12-21
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scanning electron microscope sem images - by Bioz Stars, 2026-09
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digital image analysis system  (Olympus)
98
Olympus digital image analysis system
Synthesis and characterization of aCD47-CATE nanoplatform. (A) The preparation of aCD47-CATE nanoplatform. (B) UV-Vis absorption spectra of Croc under different pH. (C) The morphology of the aCD47-CATE nanostructure as visualized by transmission electron microscopy (TEM), scale bar = 100 nm (up) and scanning electron <t>microscope</t> <t>(SEM),</t> scale bar = 200 nm (down). (D) Changes in the zeta potential that occurred during the synthesis steps for both CATE and aCD47-CATE nanoplatform. Data are presented as mean ± SD (n = 3). (E) A characteristic high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) micrograph, presented alongside the associated elemental distribution maps for the aCD47-CATE nanoplatform. (F) NIR-II thermal images of the aCD47-CATE nanoplatform in a phantom under 1064 nm laser irradiation at different power densities (0.5, 1.0, 1.5, 2.0 W/cm 2 ) for 360 s. (G) Graphs depicting the temperature rise for the aCD47-CATE NPs under different laser power at 1064 nm laser irradiation. (H) Multiple heating cycles of aCD47-CATE nanoplatform under 1.0 W/cm 2 at 1064 nm laser irradiation.
Digital Image Analysis System, supplied by Olympus, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/microscope+images/DP74+Microscope+Digital+Camera/pmc13010966-116-17-26
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digital image analysis system - by Bioz Stars, 2026-09
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witec alpha 300r raman imaging microscope  (Oxford Instruments)
99
Oxford Instruments witec alpha 300r raman imaging microscope
Synthesis and characterization of aCD47-CATE nanoplatform. (A) The preparation of aCD47-CATE nanoplatform. (B) UV-Vis absorption spectra of Croc under different pH. (C) The morphology of the aCD47-CATE nanostructure as visualized by transmission electron microscopy (TEM), scale bar = 100 nm (up) and scanning electron <t>microscope</t> <t>(SEM),</t> scale bar = 200 nm (down). (D) Changes in the zeta potential that occurred during the synthesis steps for both CATE and aCD47-CATE nanoplatform. Data are presented as mean ± SD (n = 3). (E) A characteristic high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) micrograph, presented alongside the associated elemental distribution maps for the aCD47-CATE nanoplatform. (F) NIR-II thermal images of the aCD47-CATE nanoplatform in a phantom under 1064 nm laser irradiation at different power densities (0.5, 1.0, 1.5, 2.0 W/cm 2 ) for 360 s. (G) Graphs depicting the temperature rise for the aCD47-CATE NPs under different laser power at 1064 nm laser irradiation. (H) Multiple heating cycles of aCD47-CATE nanoplatform under 1.0 W/cm 2 at 1064 nm laser irradiation.
Witec Alpha 300r Raman Imaging Microscope, supplied by Oxford Instruments, 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/microscope+images/alpha300/pmc13220855-145-13-13
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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

Synthesis and characterization of aCD47-CATE nanoplatform. (A) The preparation of aCD47-CATE nanoplatform. (B) UV-Vis absorption spectra of Croc under different pH. (C) The morphology of the aCD47-CATE nanostructure as visualized by transmission electron microscopy (TEM), scale bar = 100 nm (up) and scanning electron microscope (SEM), scale bar = 200 nm (down). (D) Changes in the zeta potential that occurred during the synthesis steps for both CATE and aCD47-CATE nanoplatform. Data are presented as mean ± SD (n = 3). (E) A characteristic high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) micrograph, presented alongside the associated elemental distribution maps for the aCD47-CATE nanoplatform. (F) NIR-II thermal images of the aCD47-CATE nanoplatform in a phantom under 1064 nm laser irradiation at different power densities (0.5, 1.0, 1.5, 2.0 W/cm 2 ) for 360 s. (G) Graphs depicting the temperature rise for the aCD47-CATE NPs under different laser power at 1064 nm laser irradiation. (H) Multiple heating cycles of aCD47-CATE nanoplatform under 1.0 W/cm 2 at 1064 nm laser irradiation.

Journal: Materials Today Bio

Article Title: Macrophage exosome-engineered nanoplatform with pH-responsive ratiometric photoacoustic and NIR-II fluorescence imaging for guided photothermal immunotherapy of hepatocellular carcinoma

doi: 10.1016/j.mtbio.2026.103058

Figure Lengend Snippet: Synthesis and characterization of aCD47-CATE nanoplatform. (A) The preparation of aCD47-CATE nanoplatform. (B) UV-Vis absorption spectra of Croc under different pH. (C) The morphology of the aCD47-CATE nanostructure as visualized by transmission electron microscopy (TEM), scale bar = 100 nm (up) and scanning electron microscope (SEM), scale bar = 200 nm (down). (D) Changes in the zeta potential that occurred during the synthesis steps for both CATE and aCD47-CATE nanoplatform. Data are presented as mean ± SD (n = 3). (E) A characteristic high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) micrograph, presented alongside the associated elemental distribution maps for the aCD47-CATE nanoplatform. (F) NIR-II thermal images of the aCD47-CATE nanoplatform in a phantom under 1064 nm laser irradiation at different power densities (0.5, 1.0, 1.5, 2.0 W/cm 2 ) for 360 s. (G) Graphs depicting the temperature rise for the aCD47-CATE NPs under different laser power at 1064 nm laser irradiation. (H) Multiple heating cycles of aCD47-CATE nanoplatform under 1.0 W/cm 2 at 1064 nm laser irradiation.

Article Snippet: Transmission electron microscope (TEM) images were captured with a JEOL JEM-2100, and Scanning Electron Microscope (SEM) images were obtained using a JEOL Model JSM-6490.

Techniques: Transmission Assay, Electron Microscopy, Microscopy, Zeta Potential Analyzer, Irradiation