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dhe fluorescent probe  (Yeasen Biotechnology)

 
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    Yeasen Biotechnology dhe fluorescent probe
    Dhe Fluorescent Probe, supplied by Yeasen Biotechnology, 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/dihydroethidium+fluorescent+probe/fluorescent+probe/pm41559402-51-0-29
    Average 86 stars, based on 1 article reviews
    dhe fluorescent probe - by Bioz Stars, 2026-11
    86/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: Nanozymes for ATP/cAMP balance restoration and ROS scavenging in inflammatory dermatosis treatment and recurrence prevention
    Article Snippet: .. Subsequently, sections were blocked with goat serum at 4 °C for 24 h. Following blocking, ROS were stained using the Dihydroethidium fluorescent probe (YEASEN, 50102ES25) by incubating sections at 37 °C in the dark for 30 min. After incubation, sections were washed three times with PBS T. Nuclei were then stained with Hoechst dye (Beyotime, C1017) for 10 min at room temperature in the dark, followed by three washes with PBST. ..

    Article Title: Nanozymes for ATP/cAMP balance restoration and ROS scavenging in inflammatory dermatosis treatment and recurrence prevention.
    Article Snippet: .. Subsequently, sections were blocked with goat serum at 4 °C for 24 h. Following blocking, ROS were stained using the Dihydroethidium fluorescent probe (YEASEN, 50102ES25) by incubating sections at 37 °C in the dark for 30 min. After incubation, sections were washed three times with PBS T. Nuclei were then stained with Hoechst dye (Beyotime, C1017) for 10 min at room temperature in the dark, followed by three washes with PBST. ..

    Staining:

    Article Title: Nanozymes for ATP/cAMP balance restoration and ROS scavenging in inflammatory dermatosis treatment and recurrence prevention
    Article Snippet: .. Subsequently, sections were blocked with goat serum at 4 °C for 24 h. Following blocking, ROS were stained using the Dihydroethidium fluorescent probe (YEASEN, 50102ES25) by incubating sections at 37 °C in the dark for 30 min. After incubation, sections were washed three times with PBS T. Nuclei were then stained with Hoechst dye (Beyotime, C1017) for 10 min at room temperature in the dark, followed by three washes with PBST. ..

    Article Title: Nanozymes for ATP/cAMP balance restoration and ROS scavenging in inflammatory dermatosis treatment and recurrence prevention.
    Article Snippet: .. Subsequently, sections were blocked with goat serum at 4 °C for 24 h. Following blocking, ROS were stained using the Dihydroethidium fluorescent probe (YEASEN, 50102ES25) by incubating sections at 37 °C in the dark for 30 min. After incubation, sections were washed three times with PBS T. Nuclei were then stained with Hoechst dye (Beyotime, C1017) for 10 min at room temperature in the dark, followed by three washes with PBST. ..

    Incubation:

    Article Title: Nanozymes for ATP/cAMP balance restoration and ROS scavenging in inflammatory dermatosis treatment and recurrence prevention
    Article Snippet: .. Subsequently, sections were blocked with goat serum at 4 °C for 24 h. Following blocking, ROS were stained using the Dihydroethidium fluorescent probe (YEASEN, 50102ES25) by incubating sections at 37 °C in the dark for 30 min. After incubation, sections were washed three times with PBS T. Nuclei were then stained with Hoechst dye (Beyotime, C1017) for 10 min at room temperature in the dark, followed by three washes with PBST. ..

    Article Title: Nanozymes for ATP/cAMP balance restoration and ROS scavenging in inflammatory dermatosis treatment and recurrence prevention.
    Article Snippet: .. Subsequently, sections were blocked with goat serum at 4 °C for 24 h. Following blocking, ROS were stained using the Dihydroethidium fluorescent probe (YEASEN, 50102ES25) by incubating sections at 37 °C in the dark for 30 min. After incubation, sections were washed three times with PBS T. Nuclei were then stained with Hoechst dye (Beyotime, C1017) for 10 min at room temperature in the dark, followed by three washes with PBST. ..



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    BMSC-Fe 3 O 4 -SMF-Exos Mitigate Intracellular ROS in Irradiated BMSCs. ( a , c ) Intracellular total ROS levels in BMSCs were evaluated utilizing the 2′,7′-dichlorodihydrofluorescein diacetate (DCF-DA) fluorescent probe, accompanied by the relevant quantitative determination. ( b , d ) Superoxide anion (O 2 − ) production in irradiated BMSCs was monitored with the DHE fluorescent probe, and concurrent quantitative analysis was implemented. ( e ) The concentration of MDA in irradiated BMSCs was quantified. ( f , g ) The levels of SOD in irradiated BMSCs were measured at the 24 h and 48 h time points, separately. n = 3; (**) p < 0.01; (***) p < 0.001, and (****) p < 0.0001.

    Journal: Bioengineering

    Article Title: Fe 3 O 4 Magnetic Nanoparticles and Static Magnetic Field Stimulated BMSC-Derived Exosomes Promoted Osteogenesis and Alleviated Oxidative Stress in Irradiated BMSCs Through miR-429/NOG Pathway

    doi: 10.3390/bioengineering13040402

    Figure Lengend Snippet: BMSC-Fe 3 O 4 -SMF-Exos Mitigate Intracellular ROS in Irradiated BMSCs. ( a , c ) Intracellular total ROS levels in BMSCs were evaluated utilizing the 2′,7′-dichlorodihydrofluorescein diacetate (DCF-DA) fluorescent probe, accompanied by the relevant quantitative determination. ( b , d ) Superoxide anion (O 2 − ) production in irradiated BMSCs was monitored with the DHE fluorescent probe, and concurrent quantitative analysis was implemented. ( e ) The concentration of MDA in irradiated BMSCs was quantified. ( f , g ) The levels of SOD in irradiated BMSCs were measured at the 24 h and 48 h time points, separately. n = 3; (**) p < 0.01; (***) p < 0.001, and (****) p < 0.0001.

    Article Snippet: Similarly, intracellular superoxide anion levels were measured using a Dihydroethidium (DHE) Superoxide Anion Fluorescent Probe Kit (G1904-100T, Servicebio, Wuhan, Hubei, China) in full accordance with the manufacturer’s instructions.

    Techniques: Irradiation, Concentration Assay