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casp3  (Bioss)


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    Structured Review

    Bioss casp3
    <t>Casp3</t> protein immunostaining images (A) and quantitative comparison between groups (B). Statistical comparisons were performed between CD133+ and CD133− groups at each LIPUS application time point (black asterisks), as well as within each group relative to the untreated 0‐min baseline (red asterisks for CD133+, blue asterisks for CD133−). Data are shown as mean ± SD. Statistical significance was evaluated using one‐way ANOVA followed by Tukey's post hoc test. * p < 0.05, ** p < 0.01, *** p < 0.001. No statistically significant difference was observed between the groups without LIPUS application in both CD133+ and CD133− cell groups. However, a significant difference was observed between the cell groups following 1‐min and 5‐min LIPUS applications ( p < 0.05 and p < 0.001). In the CD133+ cell groups, Casp3 levels increased compared to the control group (0 min) ( p < 0.001), with the maximum increase observed at 5 min of application. A similar pattern was observed in the CD133− cell group, with an increase in Casp3 protein immunostaining within the cells following LIPUS application ( p < 0.001), with the maximum increase recorded at 1 min of application.
    Casp3, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/casp3/product/Bioss
    Average 94 stars, based on 20 article reviews
    casp3 - by Bioz Stars, 2026-02
    94/100 stars

    Images

    1) Product Images from "Time‐Dependent Effects of Low‐Intensity Pulsed Ultrasound on Apoptosis and Autophagy in Malignant Melanoma Stem Cells"

    Article Title: Time‐Dependent Effects of Low‐Intensity Pulsed Ultrasound on Apoptosis and Autophagy in Malignant Melanoma Stem Cells

    Journal: Journal of Cellular and Molecular Medicine

    doi: 10.1111/jcmm.70687

    Casp3 protein immunostaining images (A) and quantitative comparison between groups (B). Statistical comparisons were performed between CD133+ and CD133− groups at each LIPUS application time point (black asterisks), as well as within each group relative to the untreated 0‐min baseline (red asterisks for CD133+, blue asterisks for CD133−). Data are shown as mean ± SD. Statistical significance was evaluated using one‐way ANOVA followed by Tukey's post hoc test. * p < 0.05, ** p < 0.01, *** p < 0.001. No statistically significant difference was observed between the groups without LIPUS application in both CD133+ and CD133− cell groups. However, a significant difference was observed between the cell groups following 1‐min and 5‐min LIPUS applications ( p < 0.05 and p < 0.001). In the CD133+ cell groups, Casp3 levels increased compared to the control group (0 min) ( p < 0.001), with the maximum increase observed at 5 min of application. A similar pattern was observed in the CD133− cell group, with an increase in Casp3 protein immunostaining within the cells following LIPUS application ( p < 0.001), with the maximum increase recorded at 1 min of application.
    Figure Legend Snippet: Casp3 protein immunostaining images (A) and quantitative comparison between groups (B). Statistical comparisons were performed between CD133+ and CD133− groups at each LIPUS application time point (black asterisks), as well as within each group relative to the untreated 0‐min baseline (red asterisks for CD133+, blue asterisks for CD133−). Data are shown as mean ± SD. Statistical significance was evaluated using one‐way ANOVA followed by Tukey's post hoc test. * p < 0.05, ** p < 0.01, *** p < 0.001. No statistically significant difference was observed between the groups without LIPUS application in both CD133+ and CD133− cell groups. However, a significant difference was observed between the cell groups following 1‐min and 5‐min LIPUS applications ( p < 0.05 and p < 0.001). In the CD133+ cell groups, Casp3 levels increased compared to the control group (0 min) ( p < 0.001), with the maximum increase observed at 5 min of application. A similar pattern was observed in the CD133− cell group, with an increase in Casp3 protein immunostaining within the cells following LIPUS application ( p < 0.001), with the maximum increase recorded at 1 min of application.

    Techniques Used: Immunostaining, Comparison, Control



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