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rat hfscs  (Procell Inc)

 
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    Structured Review

    Procell Inc rat hfscs
    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.
    Rat Hfscs, supplied by Procell Inc, 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/rat+hfscs/pmc12717658-31-1-6?v=Procell+Inc
    Average 86 stars, based on 1 article reviews
    rat hfscs - by Bioz Stars, 2026-07
    86/100 stars

    Images

    1) Product Images from "Exosomes derived from platelet-rich plasma promote hair regeneration by regulating the SIRT1/FoxO3a pathway to alleviate oxidative stress"

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

    Journal: Regenerative Therapy

    doi: 10.1016/j.reth.2025.08.005

    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.
    Figure Legend 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.

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



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    rat hfscs with melatonin  (MedChemExpress)
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    MedChemExpress rat hfscs with melatonin
    Figure 1. (A) Results of ddPCR detection of surface markers of <t>HFSCs</t> in primary cultured cell models; blue dots represent positive signal microdroplets. (B) Immunofluorescence staining of CD34 and CD29 (surface markers of HFSCs) in primary cultured cell models; scale bar, 50 µm. (C) ddPCR detection <t>of</t> <t>melatonin</t> membrane receptor MT1 and MT2 expression in HFSCs. (D) Effects of different doses of melatonin on the transcriptional level of Rora. ns, not statistically significant; * p < 0.05. Subsequent significance markers use the same notation. (E) WB detection of effects of melatonin (1000 ng/L) on RORA levels. (F) Relative expression of RORA in HFSCs after melatonin (1000 ng/L) treatment.
    Rat Hfscs With Melatonin, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rat hfscs  (Procell Inc)
    86
    Procell Inc rat hfscs
    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.
    Rat Hfscs, supplied by Procell Inc, 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/rat+hfscs/pmc12717658-31-1-6?v=Procell+Inc
    Average 86 stars, based on 1 article reviews
    rat hfscs - by Bioz Stars, 2026-07
    86/100 stars
    		  Buy from Supplier

    Image Search Results


    Figure 1. (A) Results of ddPCR detection of surface markers of HFSCs in primary cultured cell models; blue dots represent positive signal microdroplets. (B) Immunofluorescence staining of CD34 and CD29 (surface markers of HFSCs) in primary cultured cell models; scale bar, 50 µm. (C) ddPCR detection of melatonin membrane receptor MT1 and MT2 expression in HFSCs. (D) Effects of different doses of melatonin on the transcriptional level of Rora. ns, not statistically significant; * p < 0.05. Subsequent significance markers use the same notation. (E) WB detection of effects of melatonin (1000 ng/L) on RORA levels. (F) Relative expression of RORA in HFSCs after melatonin (1000 ng/L) treatment.

    Journal: Biomolecules

    Article Title: Melatonin-Mediated Circadian Rhythm Signaling Exhibits Bidirectional Regulatory Effects on the State of Hair Follicle Stem Cells.

    doi: 10.3390/biom15020226

    Figure Lengend Snippet: Figure 1. (A) Results of ddPCR detection of surface markers of HFSCs in primary cultured cell models; blue dots represent positive signal microdroplets. (B) Immunofluorescence staining of CD34 and CD29 (surface markers of HFSCs) in primary cultured cell models; scale bar, 50 µm. (C) ddPCR detection of melatonin membrane receptor MT1 and MT2 expression in HFSCs. (D) Effects of different doses of melatonin on the transcriptional level of Rora. ns, not statistically significant; * p < 0.05. Subsequent significance markers use the same notation. (E) WB detection of effects of melatonin (1000 ng/L) on RORA levels. (F) Relative expression of RORA in HFSCs after melatonin (1000 ng/L) treatment.

    Article Snippet: We treated the rat HFSCs with melatonin (MCE, HY-B0075) at final concentrations of 500 ng/L, 1000 ng/L (low dose), Biomolecules 2025, 15, 226 3 of 13 and 2000 ng/L (high dose) and set up a blank control group.

    Techniques: Cell Culture, Immunofluorescence, Staining, Membrane, Expressing

    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