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uptake function dii labeled dpc exos were successfully internalized by hfscs within 24 hours live imaging confirmed in vivo uptake of exosomes after dorsal skin injection in mice  (Exosome Diagnostics)

 
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    Exosome Diagnostics uptake function dii labeled dpc exos were successfully internalized by hfscs within 24 hours live imaging confirmed in vivo uptake of exosomes after dorsal skin injection in mice
    Uptake Function Dii Labeled Dpc Exos Were Successfully Internalized By Hfscs Within 24 Hours Live Imaging Confirmed In Vivo Uptake Of Exosomes After Dorsal Skin Injection In Mice, 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/product/hfscs/pmc12305264-60-1-0?v=Exosome+Diagnostics
    Average 86 stars, based on 1 article reviews
    uptake function dii labeled dpc exos were successfully internalized by hfscs within 24 hours live imaging confirmed in vivo uptake of exosomes after dorsal skin injection in mice - by Bioz Stars, 2026-07
    86/100 stars

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    PRP-exos treatment promotes proliferation and migration of <t>HFSCs.</t> (A) The morphology of PRP-exos was observed by TEM. (B) The exosomal markers were identified by Western blot. (C) Immunofluorescence was used to identify the <t>marker</t> <t>CK19</t> of rat HFSCs. (D and E) Calcein/PI staining and CCK-8 were used to detect proliferation of HFSCs (n = 3). (F) Wound healing assays were used to measure the migration capacity of HFSCs (n = 3). ∗p < 0.05 compared with Control; ∗∗p < 0.01 compared with Control. Data are expressed as Mean ± SD.
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    Image Search Results


    PRP-exos treatment promotes proliferation and migration of HFSCs. (A) The morphology of PRP-exos was observed by TEM. (B) The exosomal markers were identified by Western blot. (C) Immunofluorescence was used to identify the marker CK19 of rat HFSCs. (D and E) Calcein/PI staining and CCK-8 were used to detect proliferation of HFSCs (n = 3). (F) Wound healing assays were used to measure the migration capacity of HFSCs (n = 3). ∗p < 0.05 compared with Control; ∗∗p < 0.01 compared with Control. Data are expressed as Mean ± SD.

    Journal: Regenerative Therapy

    Article Title: Exosomes derived from platelet-rich plasma promote hair regeneration by regulating the SIRT1/FoxO3a pathway to alleviate oxidative stress

    doi: 10.1016/j.reth.2025.08.005

    Figure Lengend Snippet: PRP-exos treatment promotes proliferation and migration of HFSCs. (A) The morphology of PRP-exos was observed by TEM. (B) The exosomal markers were identified by Western blot. (C) Immunofluorescence was used to identify the marker CK19 of rat HFSCs. (D and E) Calcein/PI staining and CCK-8 were used to detect proliferation of HFSCs (n = 3). (F) Wound healing assays were used to measure the migration capacity of HFSCs (n = 3). ∗p < 0.05 compared with Control; ∗∗p < 0.01 compared with Control. Data are expressed as Mean ± SD.

    Article Snippet: The rat HFSCs were purchased from Procell (China), and their marker CK19 was identified by immunofluorescence.

    Techniques: Migration, Western Blot, Immunofluorescence, Marker, Staining, CCK-8 Assay, Control