Review




Structured Review

Exosome Diagnostics negative marker protein histone
Characterization and distribution of exercise-derived serum exosomes . A, Schematic diagram illustrating the proposed mode of action and therapeutic strategy. B, TEM image showing the typical cup-shaped morphology of isolated exosomes. Scale bar = 100 nm. C, Size distribution profile of exosomes measured by DLS. D, Confocal microscopy image showing the incorporation of exosomes (green) within the hydrogel matrix. Scale bar = 50 μm. E, Cellular uptake of DiO-labeled exosomes (green) by HUVECs in vitro. Nuclei were stained with DAPI (blue). Scale bar = 25 μm. F, Western blot analysis of Exosome positive <t>marker</t> proteins TSG101, CD81, HSP70 and exosome <t>negative</t> marker <t>protein</t> <t>Histone.</t> G, Flowchart for isolating exosomes from the serum of exercise and sedentary mice. H, In vivo distribution and sustained release of exosomes in cardiac tissue of MI-Exos and MI-Exos@Gel-PEG treated mice. I, Quantitative analysis of exosomal fluorescence intensity in heart tissues (n = 3). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Negative Marker Protein Histone, supplied by Exosome Diagnostics, 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/result/negative marker protein histone/product/Exosome Diagnostics
Average 86 stars, based on 1 article reviews
negative marker protein histone - by Bioz Stars, 2026-05
86/100 stars

Images

1) Product Images from "Exercise-primed exosomes in an injectable hydrogel promote myocardial repair via angiogenesis and ferroptosis inhibition"

Article Title: Exercise-primed exosomes in an injectable hydrogel promote myocardial repair via angiogenesis and ferroptosis inhibition

Journal: Materials Today Bio

doi: 10.1016/j.mtbio.2026.103035

Characterization and distribution of exercise-derived serum exosomes . A, Schematic diagram illustrating the proposed mode of action and therapeutic strategy. B, TEM image showing the typical cup-shaped morphology of isolated exosomes. Scale bar = 100 nm. C, Size distribution profile of exosomes measured by DLS. D, Confocal microscopy image showing the incorporation of exosomes (green) within the hydrogel matrix. Scale bar = 50 μm. E, Cellular uptake of DiO-labeled exosomes (green) by HUVECs in vitro. Nuclei were stained with DAPI (blue). Scale bar = 25 μm. F, Western blot analysis of Exosome positive marker proteins TSG101, CD81, HSP70 and exosome negative marker protein Histone. G, Flowchart for isolating exosomes from the serum of exercise and sedentary mice. H, In vivo distribution and sustained release of exosomes in cardiac tissue of MI-Exos and MI-Exos@Gel-PEG treated mice. I, Quantitative analysis of exosomal fluorescence intensity in heart tissues (n = 3). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Figure Legend Snippet: Characterization and distribution of exercise-derived serum exosomes . A, Schematic diagram illustrating the proposed mode of action and therapeutic strategy. B, TEM image showing the typical cup-shaped morphology of isolated exosomes. Scale bar = 100 nm. C, Size distribution profile of exosomes measured by DLS. D, Confocal microscopy image showing the incorporation of exosomes (green) within the hydrogel matrix. Scale bar = 50 μm. E, Cellular uptake of DiO-labeled exosomes (green) by HUVECs in vitro. Nuclei were stained with DAPI (blue). Scale bar = 25 μm. F, Western blot analysis of Exosome positive marker proteins TSG101, CD81, HSP70 and exosome negative marker protein Histone. G, Flowchart for isolating exosomes from the serum of exercise and sedentary mice. H, In vivo distribution and sustained release of exosomes in cardiac tissue of MI-Exos and MI-Exos@Gel-PEG treated mice. I, Quantitative analysis of exosomal fluorescence intensity in heart tissues (n = 3). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Techniques Used: Derivative Assay, Isolation, Confocal Microscopy, Labeling, In Vitro, Staining, Western Blot, Marker, In Vivo, Fluorescence



Similar Products

86
Exosome Diagnostics negative marker protein histone
Characterization and distribution of exercise-derived serum exosomes . A, Schematic diagram illustrating the proposed mode of action and therapeutic strategy. B, TEM image showing the typical cup-shaped morphology of isolated exosomes. Scale bar = 100 nm. C, Size distribution profile of exosomes measured by DLS. D, Confocal microscopy image showing the incorporation of exosomes (green) within the hydrogel matrix. Scale bar = 50 μm. E, Cellular uptake of DiO-labeled exosomes (green) by HUVECs in vitro. Nuclei were stained with DAPI (blue). Scale bar = 25 μm. F, Western blot analysis of Exosome positive <t>marker</t> proteins TSG101, CD81, HSP70 and exosome <t>negative</t> marker <t>protein</t> <t>Histone.</t> G, Flowchart for isolating exosomes from the serum of exercise and sedentary mice. H, In vivo distribution and sustained release of exosomes in cardiac tissue of MI-Exos and MI-Exos@Gel-PEG treated mice. I, Quantitative analysis of exosomal fluorescence intensity in heart tissues (n = 3). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Negative Marker Protein Histone, supplied by Exosome Diagnostics, 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/result/negative marker protein histone/product/Exosome Diagnostics
Average 86 stars, based on 1 article reviews
negative marker protein histone - by Bioz Stars, 2026-05
86/100 stars
  Buy from Supplier

Image Search Results


Characterization and distribution of exercise-derived serum exosomes . A, Schematic diagram illustrating the proposed mode of action and therapeutic strategy. B, TEM image showing the typical cup-shaped morphology of isolated exosomes. Scale bar = 100 nm. C, Size distribution profile of exosomes measured by DLS. D, Confocal microscopy image showing the incorporation of exosomes (green) within the hydrogel matrix. Scale bar = 50 μm. E, Cellular uptake of DiO-labeled exosomes (green) by HUVECs in vitro. Nuclei were stained with DAPI (blue). Scale bar = 25 μm. F, Western blot analysis of Exosome positive marker proteins TSG101, CD81, HSP70 and exosome negative marker protein Histone. G, Flowchart for isolating exosomes from the serum of exercise and sedentary mice. H, In vivo distribution and sustained release of exosomes in cardiac tissue of MI-Exos and MI-Exos@Gel-PEG treated mice. I, Quantitative analysis of exosomal fluorescence intensity in heart tissues (n = 3). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Journal: Materials Today Bio

Article Title: Exercise-primed exosomes in an injectable hydrogel promote myocardial repair via angiogenesis and ferroptosis inhibition

doi: 10.1016/j.mtbio.2026.103035

Figure Lengend Snippet: Characterization and distribution of exercise-derived serum exosomes . A, Schematic diagram illustrating the proposed mode of action and therapeutic strategy. B, TEM image showing the typical cup-shaped morphology of isolated exosomes. Scale bar = 100 nm. C, Size distribution profile of exosomes measured by DLS. D, Confocal microscopy image showing the incorporation of exosomes (green) within the hydrogel matrix. Scale bar = 50 μm. E, Cellular uptake of DiO-labeled exosomes (green) by HUVECs in vitro. Nuclei were stained with DAPI (blue). Scale bar = 25 μm. F, Western blot analysis of Exosome positive marker proteins TSG101, CD81, HSP70 and exosome negative marker protein Histone. G, Flowchart for isolating exosomes from the serum of exercise and sedentary mice. H, In vivo distribution and sustained release of exosomes in cardiac tissue of MI-Exos and MI-Exos@Gel-PEG treated mice. I, Quantitative analysis of exosomal fluorescence intensity in heart tissues (n = 3). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: F, Western blot analysis of Exosome positive marker proteins TSG101, CD81, HSP70 and exosome negative marker protein Histone.

Techniques: Derivative Assay, Isolation, Confocal Microscopy, Labeling, In Vitro, Staining, Western Blot, Marker, In Vivo, Fluorescence