cryo electron microscope Search Results


cryo arm 300  (JEOL)
93
JEOL cryo arm 300
Cryo Arm 300, supplied by JEOL, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cryo+electron+microscope/JEM-3300+Transmission+Electron+Microscope/pm37507515-291-17-20
Average 93 stars, based on 1 article reviews
cryo arm 300 - by Bioz Stars, 2026-10
93/100 stars
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cryo-electron microscopic structural characterization  (Gallus BioPharmaceuticals)
90
Gallus BioPharmaceuticals cryo-electron microscopic structural characterization
Cryo Electron Microscopic Structural Characterization, supplied by Gallus BioPharmaceuticals, 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/cryo+electron+microscope/cryo+electron+microscopic+structural+characterization/pm39924111-25-2-17
Average 90 stars, based on 1 article reviews
cryo-electron microscopic structural characterization - by Bioz Stars, 2026-10
90/100 stars
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titan krios cryo-electron microscope  (SusTech GmbH)
90
SusTech GmbH titan krios cryo-electron microscope
Titan Krios Cryo Electron Microscope, supplied by SusTech GmbH, 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/cryo+electron+microscope/cryo+electron+microscope/pm36477448-266-22-21
Average 90 stars, based on 1 article reviews
titan krios cryo-electron microscope - by Bioz Stars, 2026-10
90/100 stars
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cryo electron microscope  (TERABASE CORPORATION)
90
TERABASE CORPORATION cryo electron microscope
a Schematic illustrations of the CNF sheet attachment method. CNF sheets were directly attached to organ surfaces, where they absorbed <t>ascites</t> <t>EVs.</t> After detachment from the organ surface, the sheets were completely dried out, and the cellulose nanofibers were aggregated. CNF sheets were washed, and cellulose nanofibers were opened. Finally, the EVs were released from the CNF sheets. b Representative photos of CNF sheet attachment to the peroneal wall. c , d The size distribution and concentration obtained by nanoparticle tracking assays (NTAs) for mouse ascites EVs by using CNF sheets. n = 10. e <t>Cryo-EM</t> image of EVs recovered from CNF sheet EVs from mouse ascites. f Single-particle quantification was performed using the ExoView platform. n = 3 from independent mice. The numbers of detected EVs are displayed in bar charts. g Schematic illustrations of CNF sheet attachment sites at the liver surface or peritoneum. h A heatmap showing 17 differentially expressed miRNAs from CNF sheet EVs based on small RNA-seq. n = 5: EVs from the liver surface and n = 5: EVs from the peritoneum. Adjusted P -values < 0.05, |log2FC | > 1. c , d – f Data are presented as mean values with SD. Each experiment was repeated at least three times ( c , d – f ).
Cryo Electron Microscope, supplied by TERABASE CORPORATION, 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/cryo+electron+microscope/cryo+electron+microscope/pmc10632339-299-7-10
Average 90 stars, based on 1 article reviews
cryo electron microscope - by Bioz Stars, 2026-10
90/100 stars
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cryo-electron microscope techni t12  (Techni Inc)
90
Techni Inc cryo-electron microscope techni t12
a Schematic illustrations of the CNF sheet attachment method. CNF sheets were directly attached to organ surfaces, where they absorbed <t>ascites</t> <t>EVs.</t> After detachment from the organ surface, the sheets were completely dried out, and the cellulose nanofibers were aggregated. CNF sheets were washed, and cellulose nanofibers were opened. Finally, the EVs were released from the CNF sheets. b Representative photos of CNF sheet attachment to the peroneal wall. c , d The size distribution and concentration obtained by nanoparticle tracking assays (NTAs) for mouse ascites EVs by using CNF sheets. n = 10. e <t>Cryo-EM</t> image of EVs recovered from CNF sheet EVs from mouse ascites. f Single-particle quantification was performed using the ExoView platform. n = 3 from independent mice. The numbers of detected EVs are displayed in bar charts. g Schematic illustrations of CNF sheet attachment sites at the liver surface or peritoneum. h A heatmap showing 17 differentially expressed miRNAs from CNF sheet EVs based on small RNA-seq. n = 5: EVs from the liver surface and n = 5: EVs from the peritoneum. Adjusted P -values < 0.05, |log2FC | > 1. c , d – f Data are presented as mean values with SD. Each experiment was repeated at least three times ( c , d – f ).
Cryo Electron Microscope Techni T12, supplied by Techni Inc, 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/cryo+electron+microscope/cryo+electron+microscope+techni+t12/pmc03286910-252-5-5
Average 90 stars, based on 1 article reviews
cryo-electron microscope techni t12 - by Bioz Stars, 2026-10
90/100 stars
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cryo-electron microscope  (NanoImaging Services Inc)
90
NanoImaging Services Inc cryo-electron microscope
a Schematic illustrations of the CNF sheet attachment method. CNF sheets were directly attached to organ surfaces, where they absorbed <t>ascites</t> <t>EVs.</t> After detachment from the organ surface, the sheets were completely dried out, and the cellulose nanofibers were aggregated. CNF sheets were washed, and cellulose nanofibers were opened. Finally, the EVs were released from the CNF sheets. b Representative photos of CNF sheet attachment to the peroneal wall. c , d The size distribution and concentration obtained by nanoparticle tracking assays (NTAs) for mouse ascites EVs by using CNF sheets. n = 10. e <t>Cryo-EM</t> image of EVs recovered from CNF sheet EVs from mouse ascites. f Single-particle quantification was performed using the ExoView platform. n = 3 from independent mice. The numbers of detected EVs are displayed in bar charts. g Schematic illustrations of CNF sheet attachment sites at the liver surface or peritoneum. h A heatmap showing 17 differentially expressed miRNAs from CNF sheet EVs based on small RNA-seq. n = 5: EVs from the liver surface and n = 5: EVs from the peritoneum. Adjusted P -values < 0.05, |log2FC | > 1. c , d – f Data are presented as mean values with SD. Each experiment was repeated at least three times ( c , d – f ).
Cryo Electron Microscope, supplied by NanoImaging Services Inc, 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/cryo+electron+microscope/cryo+electron+microscope/10__21769_slash_bioprotoc__5099-535-21-9
Average 90 stars, based on 1 article reviews
cryo-electron microscope - by Bioz Stars, 2026-10
90/100 stars
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cryo-electron microscope sustech titan krios  (SusTech GmbH)
90
SusTech GmbH cryo-electron microscope sustech titan krios
a Schematic illustrations of the CNF sheet attachment method. CNF sheets were directly attached to organ surfaces, where they absorbed <t>ascites</t> <t>EVs.</t> After detachment from the organ surface, the sheets were completely dried out, and the cellulose nanofibers were aggregated. CNF sheets were washed, and cellulose nanofibers were opened. Finally, the EVs were released from the CNF sheets. b Representative photos of CNF sheet attachment to the peroneal wall. c , d The size distribution and concentration obtained by nanoparticle tracking assays (NTAs) for mouse ascites EVs by using CNF sheets. n = 10. e <t>Cryo-EM</t> image of EVs recovered from CNF sheet EVs from mouse ascites. f Single-particle quantification was performed using the ExoView platform. n = 3 from independent mice. The numbers of detected EVs are displayed in bar charts. g Schematic illustrations of CNF sheet attachment sites at the liver surface or peritoneum. h A heatmap showing 17 differentially expressed miRNAs from CNF sheet EVs based on small RNA-seq. n = 5: EVs from the liver surface and n = 5: EVs from the peritoneum. Adjusted P -values < 0.05, |log2FC | > 1. c , d – f Data are presented as mean values with SD. Each experiment was repeated at least three times ( c , d – f ).
Cryo Electron Microscope Sustech Titan Krios, supplied by SusTech GmbH, 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/cryo+electron+microscope/cryo+electron+microscope+sustech+titan+krios/pm39516663-109-16-15
Average 90 stars, based on 1 article reviews
cryo-electron microscope sustech titan krios - by Bioz Stars, 2026-10
90/100 stars
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cryo-scanning electron microscope cryo-sem  (NanoLab Inc)
90
NanoLab Inc cryo-scanning electron microscope cryo-sem
a Schematic illustrations of the CNF sheet attachment method. CNF sheets were directly attached to organ surfaces, where they absorbed <t>ascites</t> <t>EVs.</t> After detachment from the organ surface, the sheets were completely dried out, and the cellulose nanofibers were aggregated. CNF sheets were washed, and cellulose nanofibers were opened. Finally, the EVs were released from the CNF sheets. b Representative photos of CNF sheet attachment to the peroneal wall. c , d The size distribution and concentration obtained by nanoparticle tracking assays (NTAs) for mouse ascites EVs by using CNF sheets. n = 10. e <t>Cryo-EM</t> image of EVs recovered from CNF sheet EVs from mouse ascites. f Single-particle quantification was performed using the ExoView platform. n = 3 from independent mice. The numbers of detected EVs are displayed in bar charts. g Schematic illustrations of CNF sheet attachment sites at the liver surface or peritoneum. h A heatmap showing 17 differentially expressed miRNAs from CNF sheet EVs based on small RNA-seq. n = 5: EVs from the liver surface and n = 5: EVs from the peritoneum. Adjusted P -values < 0.05, |log2FC | > 1. c , d – f Data are presented as mean values with SD. Each experiment was repeated at least three times ( c , d – f ).
Cryo Scanning Electron Microscope Cryo Sem, supplied by NanoLab Inc, 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/cryo+electron+microscope/cryo+scanning+electron+microscope+cryo+sem/10__1016_slash_j__foodhyd__2020__105766-126-0-8
Average 90 stars, based on 1 article reviews
cryo-scanning electron microscope cryo-sem - by Bioz Stars, 2026-10
90/100 stars
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cryo-electron microscope  (Siemens AG)
90
Siemens AG cryo-electron microscope
a Schematic illustrations of the CNF sheet attachment method. CNF sheets were directly attached to organ surfaces, where they absorbed <t>ascites</t> <t>EVs.</t> After detachment from the organ surface, the sheets were completely dried out, and the cellulose nanofibers were aggregated. CNF sheets were washed, and cellulose nanofibers were opened. Finally, the EVs were released from the CNF sheets. b Representative photos of CNF sheet attachment to the peroneal wall. c , d The size distribution and concentration obtained by nanoparticle tracking assays (NTAs) for mouse ascites EVs by using CNF sheets. n = 10. e <t>Cryo-EM</t> image of EVs recovered from CNF sheet EVs from mouse ascites. f Single-particle quantification was performed using the ExoView platform. n = 3 from independent mice. The numbers of detected EVs are displayed in bar charts. g Schematic illustrations of CNF sheet attachment sites at the liver surface or peritoneum. h A heatmap showing 17 differentially expressed miRNAs from CNF sheet EVs based on small RNA-seq. n = 5: EVs from the liver surface and n = 5: EVs from the peritoneum. Adjusted P -values < 0.05, |log2FC | > 1. c , d – f Data are presented as mean values with SD. Each experiment was repeated at least three times ( c , d – f ).
Cryo Electron Microscope, supplied by Siemens AG, 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/cryo+electron+microscope/cryo+electron+microscope/pm07441748-8-48-15
Average 90 stars, based on 1 article reviews
cryo-electron microscope - by Bioz Stars, 2026-10
90/100 stars
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jem-3100f transmission electron microscope  (JEOL)
95
JEOL jem-3100f transmission electron microscope
a Schematic illustrations of the CNF sheet attachment method. CNF sheets were directly attached to organ surfaces, where they absorbed <t>ascites</t> <t>EVs.</t> After detachment from the organ surface, the sheets were completely dried out, and the cellulose nanofibers were aggregated. CNF sheets were washed, and cellulose nanofibers were opened. Finally, the EVs were released from the CNF sheets. b Representative photos of CNF sheet attachment to the peroneal wall. c , d The size distribution and concentration obtained by nanoparticle tracking assays (NTAs) for mouse ascites EVs by using CNF sheets. n = 10. e <t>Cryo-EM</t> image of EVs recovered from CNF sheet EVs from mouse ascites. f Single-particle quantification was performed using the ExoView platform. n = 3 from independent mice. The numbers of detected EVs are displayed in bar charts. g Schematic illustrations of CNF sheet attachment sites at the liver surface or peritoneum. h A heatmap showing 17 differentially expressed miRNAs from CNF sheet EVs based on small RNA-seq. n = 5: EVs from the liver surface and n = 5: EVs from the peritoneum. Adjusted P -values < 0.05, |log2FC | > 1. c , d – f Data are presented as mean values with SD. Each experiment was repeated at least three times ( c , d – f ).
Jem 3100f Transmission Electron Microscope, supplied by JEOL, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cryo+electron+microscope/JEM-3100F+Transmission+Electron+Microscope/custom%40jem-3100f%4031372759
Average 95 stars, based on 1 article reviews
jem-3100f transmission electron microscope - by Bioz Stars, 2026-10
95/100 stars
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Image Search Results


a Schematic illustrations of the CNF sheet attachment method. CNF sheets were directly attached to organ surfaces, where they absorbed ascites EVs. After detachment from the organ surface, the sheets were completely dried out, and the cellulose nanofibers were aggregated. CNF sheets were washed, and cellulose nanofibers were opened. Finally, the EVs were released from the CNF sheets. b Representative photos of CNF sheet attachment to the peroneal wall. c , d The size distribution and concentration obtained by nanoparticle tracking assays (NTAs) for mouse ascites EVs by using CNF sheets. n = 10. e Cryo-EM image of EVs recovered from CNF sheet EVs from mouse ascites. f Single-particle quantification was performed using the ExoView platform. n = 3 from independent mice. The numbers of detected EVs are displayed in bar charts. g Schematic illustrations of CNF sheet attachment sites at the liver surface or peritoneum. h A heatmap showing 17 differentially expressed miRNAs from CNF sheet EVs based on small RNA-seq. n = 5: EVs from the liver surface and n = 5: EVs from the peritoneum. Adjusted P -values < 0.05, |log2FC | > 1. c , d – f Data are presented as mean values with SD. Each experiment was repeated at least three times ( c , d – f ).

Journal: Nature Communications

Article Title: Spatial exosome analysis using cellulose nanofiber sheets reveals the location heterogeneity of extracellular vesicles

doi: 10.1038/s41467-023-42593-9

Figure Lengend Snippet: a Schematic illustrations of the CNF sheet attachment method. CNF sheets were directly attached to organ surfaces, where they absorbed ascites EVs. After detachment from the organ surface, the sheets were completely dried out, and the cellulose nanofibers were aggregated. CNF sheets were washed, and cellulose nanofibers were opened. Finally, the EVs were released from the CNF sheets. b Representative photos of CNF sheet attachment to the peroneal wall. c , d The size distribution and concentration obtained by nanoparticle tracking assays (NTAs) for mouse ascites EVs by using CNF sheets. n = 10. e Cryo-EM image of EVs recovered from CNF sheet EVs from mouse ascites. f Single-particle quantification was performed using the ExoView platform. n = 3 from independent mice. The numbers of detected EVs are displayed in bar charts. g Schematic illustrations of CNF sheet attachment sites at the liver surface or peritoneum. h A heatmap showing 17 differentially expressed miRNAs from CNF sheet EVs based on small RNA-seq. n = 5: EVs from the liver surface and n = 5: EVs from the peritoneum. Adjusted P -values < 0.05, |log2FC | > 1. c , d – f Data are presented as mean values with SD. Each experiment was repeated at least three times ( c , d – f ).

Article Snippet: The isolated EVs were visualized using a cryo electron microscope (Terabase Inc., Okazaki, Japan) that can generate high-contrast images of the nanostructures of biological materials without staining procedures that may damage the samples.

Techniques: Concentration Assay, Cryo-EM Sample Prep, Single Particle, RNA Sequencing Assay

a Illustrative photos of CNF sheets attached to ex vivo human cancer tumors. The right 4 panels indicate CNF sheet attachment, and the left panel indicates CNF sheet soaking for ascites. b Cryo-EM image of EVs recovered from CNF sheet EVs on the tumor surface. c A heatmap showing differentially expressed miRNAs from CNF sheet EVs or tissues based on small RNA-seq. n = 3 each: tumor surface CNF sheet, ascites CNF sheet and cancer tissue. d PCA mapping of miRNA expression, n = 3 each: tumor surface CNF sheet, ascites CNF sheet cancer tissue, serum_ CNF and urine CNF sheet. e Dot plot showing the correlation of miRNA expression in tumor surface CNF sheets vs. cancer tissue and ascites CNF sheets and cancer tissue. f , g Schematic illustrations of the location of samples and bar charts represent relative miRNA expression. n = 3 from independent locations. Data are presented as mean values with SD. The values in the left graph were normalized to tissue miRNA expression, and those in the right graph were normalized to ascites EVs. n = 3 ( h ) PCA mapping and illustrative photos from patient 2 focusing on tumor fluid profiles. i PCA mapping and illustrative photos from patient 2 focusing on metastatic tumors in the greater omentum.

Journal: Nature Communications

Article Title: Spatial exosome analysis using cellulose nanofiber sheets reveals the location heterogeneity of extracellular vesicles

doi: 10.1038/s41467-023-42593-9

Figure Lengend Snippet: a Illustrative photos of CNF sheets attached to ex vivo human cancer tumors. The right 4 panels indicate CNF sheet attachment, and the left panel indicates CNF sheet soaking for ascites. b Cryo-EM image of EVs recovered from CNF sheet EVs on the tumor surface. c A heatmap showing differentially expressed miRNAs from CNF sheet EVs or tissues based on small RNA-seq. n = 3 each: tumor surface CNF sheet, ascites CNF sheet and cancer tissue. d PCA mapping of miRNA expression, n = 3 each: tumor surface CNF sheet, ascites CNF sheet cancer tissue, serum_ CNF and urine CNF sheet. e Dot plot showing the correlation of miRNA expression in tumor surface CNF sheets vs. cancer tissue and ascites CNF sheets and cancer tissue. f , g Schematic illustrations of the location of samples and bar charts represent relative miRNA expression. n = 3 from independent locations. Data are presented as mean values with SD. The values in the left graph were normalized to tissue miRNA expression, and those in the right graph were normalized to ascites EVs. n = 3 ( h ) PCA mapping and illustrative photos from patient 2 focusing on tumor fluid profiles. i PCA mapping and illustrative photos from patient 2 focusing on metastatic tumors in the greater omentum.

Article Snippet: The isolated EVs were visualized using a cryo electron microscope (Terabase Inc., Okazaki, Japan) that can generate high-contrast images of the nanostructures of biological materials without staining procedures that may damage the samples.

Techniques: Ex Vivo, Cryo-EM Sample Prep, RNA Sequencing Assay, Expressing