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caspase 3 activity assay kit  (Beyotime)


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    Structured Review

    Beyotime caspase 3 activity assay kit
    Glibenclamide disrupted SUR1-PARP1 interaction to restore DNA repair and attenuate apoptosis and inflammation in HBE cells (A) Schematic diagram of HBE cells with different treatments, followed by RNA sequencing analysis. Groups: control, 20 ng/mL; TNF-α, 100 μmol/L; glibenclamide plus TNF-α. n = 2 per group. (B) Venn diagram of differentially expressed genes. (C) GO and KEGG enrichment analyses of 280 genes in the intersection shown in (B). (D) RT-qPCR analysis of HBE cells with different treatments as indicated. (E) Co-immunoprecipitation assay in HBE cells transfected with FLAG-SUR1 plasmids and treated with 20 ng/mL TNF-α or 100 μmol/L glibenclamide as indicated. L.E., long exposure. (F) HBE cells were treated as in (E), then subjected to cytoplasmic and nuclear protein fractionation followed by western blotting. Cyto, cytoplasm; Nu, nucleus. (G) Western blot analysis of HBE cells pretreated with 100 μmol/L glibenclamide for 30 min followed by TNF-α or LPS co-treatment for 1 h. (H–J) ROS <t>production,</t> <t>caspase-3</t> activity, and apoptosis in HBE cells under indicated treatments. (K–M) HBE cells were pretreated with 100 μmol/L glibenclamide, 5 μmol/L olaparib, or their combination for 24 h, followed by 20 ng/mL TNF-α stimulation, and subjected to western blotting, caspase-3 activity assay, and apoptosis analysis by flow cytometry. Gli, glibenclamide. Data are presented as mean ± SD ( n = 3). ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. GO and KEGG enrichment analyses in (C) were performed using a hypergeometric test with false discovery rate (FDR) correction. Data in (D) and (G–M) were analyzed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Representative images are shown.
    Caspase 3 Activity Assay Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 97/100, based on 4133 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/caspase+3+activity+assay+kit/Caspase+3+Activity+Assay+Kit/pmc13673107-31-0-6
    Average 97 stars, based on 4133 article reviews
    caspase 3 activity assay kit - by Bioz Stars, 2026-10
    97/100 stars

    Images

    1) Product Images from "Sulfonylurea receptor 1 deficiency alleviates acute lung injury by activating PARP1 in epithelial cells"

    Article Title: Sulfonylurea receptor 1 deficiency alleviates acute lung injury by activating PARP1 in epithelial cells

    Journal: iScience

    doi: 10.1016/j.isci.2026.117627

    Glibenclamide disrupted SUR1-PARP1 interaction to restore DNA repair and attenuate apoptosis and inflammation in HBE cells (A) Schematic diagram of HBE cells with different treatments, followed by RNA sequencing analysis. Groups: control, 20 ng/mL; TNF-α, 100 μmol/L; glibenclamide plus TNF-α. n = 2 per group. (B) Venn diagram of differentially expressed genes. (C) GO and KEGG enrichment analyses of 280 genes in the intersection shown in (B). (D) RT-qPCR analysis of HBE cells with different treatments as indicated. (E) Co-immunoprecipitation assay in HBE cells transfected with FLAG-SUR1 plasmids and treated with 20 ng/mL TNF-α or 100 μmol/L glibenclamide as indicated. L.E., long exposure. (F) HBE cells were treated as in (E), then subjected to cytoplasmic and nuclear protein fractionation followed by western blotting. Cyto, cytoplasm; Nu, nucleus. (G) Western blot analysis of HBE cells pretreated with 100 μmol/L glibenclamide for 30 min followed by TNF-α or LPS co-treatment for 1 h. (H–J) ROS production, caspase-3 activity, and apoptosis in HBE cells under indicated treatments. (K–M) HBE cells were pretreated with 100 μmol/L glibenclamide, 5 μmol/L olaparib, or their combination for 24 h, followed by 20 ng/mL TNF-α stimulation, and subjected to western blotting, caspase-3 activity assay, and apoptosis analysis by flow cytometry. Gli, glibenclamide. Data are presented as mean ± SD ( n = 3). ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. GO and KEGG enrichment analyses in (C) were performed using a hypergeometric test with false discovery rate (FDR) correction. Data in (D) and (G–M) were analyzed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Representative images are shown.
    Figure Legend Snippet: Glibenclamide disrupted SUR1-PARP1 interaction to restore DNA repair and attenuate apoptosis and inflammation in HBE cells (A) Schematic diagram of HBE cells with different treatments, followed by RNA sequencing analysis. Groups: control, 20 ng/mL; TNF-α, 100 μmol/L; glibenclamide plus TNF-α. n = 2 per group. (B) Venn diagram of differentially expressed genes. (C) GO and KEGG enrichment analyses of 280 genes in the intersection shown in (B). (D) RT-qPCR analysis of HBE cells with different treatments as indicated. (E) Co-immunoprecipitation assay in HBE cells transfected with FLAG-SUR1 plasmids and treated with 20 ng/mL TNF-α or 100 μmol/L glibenclamide as indicated. L.E., long exposure. (F) HBE cells were treated as in (E), then subjected to cytoplasmic and nuclear protein fractionation followed by western blotting. Cyto, cytoplasm; Nu, nucleus. (G) Western blot analysis of HBE cells pretreated with 100 μmol/L glibenclamide for 30 min followed by TNF-α or LPS co-treatment for 1 h. (H–J) ROS production, caspase-3 activity, and apoptosis in HBE cells under indicated treatments. (K–M) HBE cells were pretreated with 100 μmol/L glibenclamide, 5 μmol/L olaparib, or their combination for 24 h, followed by 20 ng/mL TNF-α stimulation, and subjected to western blotting, caspase-3 activity assay, and apoptosis analysis by flow cytometry. Gli, glibenclamide. Data are presented as mean ± SD ( n = 3). ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. GO and KEGG enrichment analyses in (C) were performed using a hypergeometric test with false discovery rate (FDR) correction. Data in (D) and (G–M) were analyzed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Representative images are shown.

    Techniques Used: RNA Sequencing, Analysis, Control, Quantitative RT-PCR, Co-Immunoprecipitation Assay, Transfection, Fractionation, Western Blot, Activity Assay, Caspase-3 Activity Assay, Flow Cytometry


    Figure Legend Snippet:

    Techniques Used: Cell-Signaling, Recombinant, Transfection, Caspase-3 Activity Assay, Protein Extraction, Knock-Out, Sequencing, Control, Plasmid Preparation, Software, Analysis

    Related Articles

    Activity Assay:

    Article Title: Spodoptera exigua Caspase-4 Enhances the Virulence of Baculovirus by Promoting Host Cell Apoptosis.
    Article Snippet: The fixed cells were then stained with DAPI (1 μg/mL) for 5min and photographed under an epifluorescence microscope (EVOS FL, Thermo Fisher Scientific, Waltham, MA, USA). .. To analyze the enzyme activity of SeCaspase-4, Se-3 cells transfected with SeCaspase-4-GFPpBlue and SeCaspase-1-GFPpBlue were lysed, and the degradation activities of SeCaspase-4 and SeCaspase-1 toward the substrates of mammalian casepase-9 (Ac-LEHD-pNA) and caspase3 (Ac-DEVD-pNA) were detected using a Caspase 9 Activity Assay Kit and a Caspase 3 Activity Assay Kit (Beyotime, Shanghai, China), respectively. .. Briefly, the total proteins of the transfected cells were extracted using the lysis buffers supplied with these two kits, and their concentrations were measured using the Bradford method (Beyotime, Shanghai, China); then, the total proteins were incubated with the specific substrates, Ac-DEVD-pNA and Ac-LEHD-pNA.

    Article Title: XopA: a novel type III secretion system effector in Xenorhabdus that modulates host cell responses through apoptosis, autophagy, and immune evasion
    Article Snippet: In the determination of cell activity, the cells were detected by the MTT kit (C0009S, Beyotime) after transfection for 24 h and 48 h. When the cell clone formation was determined, the cells were continuously cultured for 14 days after transfection, fixed with ethanol, and counted after crystal violet staining. .. For scratch repair, the transfected cells were subjected to a 10 μL sterile pipette tip to form an equal-width scratch, and the width of the scratch was recorded every 24 h. Caspase-3 activity was detected by Caspase-3 activity assay kit (C1073S, Beyotime) 24 h after transfection. ..

    Article Title: NOTCH3-R544C mutation drives endothelial dysfunction through inflammation, migration impairment, and lipid dysregulation.
    Article Snippet: Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene.. Previous research has predominantly focused on vascular smooth muscle cell pathology, whereas the role of brain microvascular endothelial cells (BMECs) in the disease remains unclear.. Objective: To investigate the impact of the NOTCH3-R544C mutation on BMECs function and to elucidate the underlying mechanisms of endothelial dysfunction in CADASIL.

    Article Title: Rational design of FAP-targeted sEVs delivered by microneedles for precision treatment of hypertrophic scars via ferroptosis in hypertrophic scar fibroblasts
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    Article Title: Bone Marrow Macrophage STING Signaling is a Direct Nexus Linking Marrow Adipose Expansion to NAD + Depletion and Osteogenic Decline in Skeletal Aging
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    Article Snippet: .. Specifically, a Caspase‐3 Activity Assay Kit (Beyotime, C1116) and a Caspase‐9 Activity Assay Kit (Beyotime, C1158) were respectively utilized according to the manufacturer's instructions. ..

    Article Title: Spodoptera exigua Caspase‑4 Enhances the Virulence of Baculovirus by Promoting Host Cell Apoptosis
    Article Snippet: The fixed cells were then stained with DAPI (1 μg/mL) for 5 min and photographed under an epifluorescence microscope (EVOS FL, Thermo Fisher Scientific, Waltham, MA, USA). .. To analyze the enzyme activity of SeCaspase-4, Se-3 cells transfected with SeCaspase-4-GFPpBlue and SeCaspase-1-GFPpBlue were lysed, and the degradation activities of SeCaspase-4 and SeCaspase-1 toward the substrates of mammalian casepase-9 (Ac-LEHD- p NA) and caspase-3 (Ac-DEVD- p NA) were detected using a Caspase 9 Activity Assay Kit and a Caspase 3 Activity Assay Kit (Beyotime, Shanghai, China), respectively. .. Briefly, the total proteins of the transfected cells were extracted using the lysis buffers supplied with these two kits, and their concentrations were measured using the Bradford method (Beyotime, Shanghai, China); then, the total proteins were incubated with the specific substrates, Ac-DEVD- p NA and Ac-LEHD- p NA.

    Transfection:

    Article Title: Spodoptera exigua Caspase-4 Enhances the Virulence of Baculovirus by Promoting Host Cell Apoptosis.
    Article Snippet: The fixed cells were then stained with DAPI (1 μg/mL) for 5min and photographed under an epifluorescence microscope (EVOS FL, Thermo Fisher Scientific, Waltham, MA, USA). .. To analyze the enzyme activity of SeCaspase-4, Se-3 cells transfected with SeCaspase-4-GFPpBlue and SeCaspase-1-GFPpBlue were lysed, and the degradation activities of SeCaspase-4 and SeCaspase-1 toward the substrates of mammalian casepase-9 (Ac-LEHD-pNA) and caspase3 (Ac-DEVD-pNA) were detected using a Caspase 9 Activity Assay Kit and a Caspase 3 Activity Assay Kit (Beyotime, Shanghai, China), respectively. .. Briefly, the total proteins of the transfected cells were extracted using the lysis buffers supplied with these two kits, and their concentrations were measured using the Bradford method (Beyotime, Shanghai, China); then, the total proteins were incubated with the specific substrates, Ac-DEVD-pNA and Ac-LEHD-pNA.

    Article Title: XopA: a novel type III secretion system effector in Xenorhabdus that modulates host cell responses through apoptosis, autophagy, and immune evasion
    Article Snippet: In the determination of cell activity, the cells were detected by the MTT kit (C0009S, Beyotime) after transfection for 24 h and 48 h. When the cell clone formation was determined, the cells were continuously cultured for 14 days after transfection, fixed with ethanol, and counted after crystal violet staining. .. For scratch repair, the transfected cells were subjected to a 10 μL sterile pipette tip to form an equal-width scratch, and the width of the scratch was recorded every 24 h. Caspase-3 activity was detected by Caspase-3 activity assay kit (C1073S, Beyotime) 24 h after transfection. ..

    Article Title: Spodoptera exigua Caspase‑4 Enhances the Virulence of Baculovirus by Promoting Host Cell Apoptosis
    Article Snippet: The fixed cells were then stained with DAPI (1 μg/mL) for 5 min and photographed under an epifluorescence microscope (EVOS FL, Thermo Fisher Scientific, Waltham, MA, USA). .. To analyze the enzyme activity of SeCaspase-4, Se-3 cells transfected with SeCaspase-4-GFPpBlue and SeCaspase-1-GFPpBlue were lysed, and the degradation activities of SeCaspase-4 and SeCaspase-1 toward the substrates of mammalian casepase-9 (Ac-LEHD- p NA) and caspase-3 (Ac-DEVD- p NA) were detected using a Caspase 9 Activity Assay Kit and a Caspase 3 Activity Assay Kit (Beyotime, Shanghai, China), respectively. .. Briefly, the total proteins of the transfected cells were extracted using the lysis buffers supplied with these two kits, and their concentrations were measured using the Bradford method (Beyotime, Shanghai, China); then, the total proteins were incubated with the specific substrates, Ac-DEVD- p NA and Ac-LEHD- p NA.

    Caspase-3 Activity Assay:

    Article Title: Spodoptera exigua Caspase-4 Enhances the Virulence of Baculovirus by Promoting Host Cell Apoptosis.
    Article Snippet: The fixed cells were then stained with DAPI (1 μg/mL) for 5min and photographed under an epifluorescence microscope (EVOS FL, Thermo Fisher Scientific, Waltham, MA, USA). .. To analyze the enzyme activity of SeCaspase-4, Se-3 cells transfected with SeCaspase-4-GFPpBlue and SeCaspase-1-GFPpBlue were lysed, and the degradation activities of SeCaspase-4 and SeCaspase-1 toward the substrates of mammalian casepase-9 (Ac-LEHD-pNA) and caspase3 (Ac-DEVD-pNA) were detected using a Caspase 9 Activity Assay Kit and a Caspase 3 Activity Assay Kit (Beyotime, Shanghai, China), respectively. .. Briefly, the total proteins of the transfected cells were extracted using the lysis buffers supplied with these two kits, and their concentrations were measured using the Bradford method (Beyotime, Shanghai, China); then, the total proteins were incubated with the specific substrates, Ac-DEVD-pNA and Ac-LEHD-pNA.

    Article Title: XopA: a novel type III secretion system effector in Xenorhabdus that modulates host cell responses through apoptosis, autophagy, and immune evasion
    Article Snippet: In the determination of cell activity, the cells were detected by the MTT kit (C0009S, Beyotime) after transfection for 24 h and 48 h. When the cell clone formation was determined, the cells were continuously cultured for 14 days after transfection, fixed with ethanol, and counted after crystal violet staining. .. For scratch repair, the transfected cells were subjected to a 10 μL sterile pipette tip to form an equal-width scratch, and the width of the scratch was recorded every 24 h. Caspase-3 activity was detected by Caspase-3 activity assay kit (C1073S, Beyotime) 24 h after transfection. ..

    Article Title: Sulfonylurea receptor 1 deficiency alleviates acute lung injury by activating PARP1 in epithelial cells
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    Article Title: NOTCH3-R544C mutation drives endothelial dysfunction through inflammation, migration impairment, and lipid dysregulation.
    Article Snippet: Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene.. Previous research has predominantly focused on vascular smooth muscle cell pathology, whereas the role of brain microvascular endothelial cells (BMECs) in the disease remains unclear.. Objective: To investigate the impact of the NOTCH3-R544C mutation on BMECs function and to elucidate the underlying mechanisms of endothelial dysfunction in CADASIL.

    Article Title: Rational design of FAP-targeted sEVs delivered by microneedles for precision treatment of hypertrophic scars via ferroptosis in hypertrophic scar fibroblasts
    Article Snippet: .. Caspase-3 activity was measured using a caspase-3 activity assay kit (Beyotime, C1115) according to the manufacturer's instructions. ..

    Article Title: Bone Marrow Macrophage STING Signaling is a Direct Nexus Linking Marrow Adipose Expansion to NAD + Depletion and Osteogenic Decline in Skeletal Aging
    Article Snippet: Cell lysates were rapidly mixed with the ATP detection working solution, and chemiluminescence was measured using a luminometric plate reader (Promega Biotech Co. Ltd., China). .. Caspase‐3 activity was measured using the Caspase‐3 Activity Assay Kit (Beyotime, C1115) according to the manufacturer's instructions. ..

    Article Title: Gastrodia elata –Derived Parishin Extracts Attenuate Aging by Modulating Oxidative Stress, Inflammation, Apoptosis, and Metabolism
    Article Snippet: .. Specifically, a Caspase‐3 Activity Assay Kit (Beyotime, C1116) and a Caspase‐9 Activity Assay Kit (Beyotime, C1158) were respectively utilized according to the manufacturer's instructions. ..

    Article Title: Spodoptera exigua Caspase‑4 Enhances the Virulence of Baculovirus by Promoting Host Cell Apoptosis
    Article Snippet: The fixed cells were then stained with DAPI (1 μg/mL) for 5 min and photographed under an epifluorescence microscope (EVOS FL, Thermo Fisher Scientific, Waltham, MA, USA). .. To analyze the enzyme activity of SeCaspase-4, Se-3 cells transfected with SeCaspase-4-GFPpBlue and SeCaspase-1-GFPpBlue were lysed, and the degradation activities of SeCaspase-4 and SeCaspase-1 toward the substrates of mammalian casepase-9 (Ac-LEHD- p NA) and caspase-3 (Ac-DEVD- p NA) were detected using a Caspase 9 Activity Assay Kit and a Caspase 3 Activity Assay Kit (Beyotime, Shanghai, China), respectively. .. Briefly, the total proteins of the transfected cells were extracted using the lysis buffers supplied with these two kits, and their concentrations were measured using the Bradford method (Beyotime, Shanghai, China); then, the total proteins were incubated with the specific substrates, Ac-DEVD- p NA and Ac-LEHD- p NA.

    Sterility:

    Article Title: XopA: a novel type III secretion system effector in Xenorhabdus that modulates host cell responses through apoptosis, autophagy, and immune evasion
    Article Snippet: In the determination of cell activity, the cells were detected by the MTT kit (C0009S, Beyotime) after transfection for 24 h and 48 h. When the cell clone formation was determined, the cells were continuously cultured for 14 days after transfection, fixed with ethanol, and counted after crystal violet staining. .. For scratch repair, the transfected cells were subjected to a 10 μL sterile pipette tip to form an equal-width scratch, and the width of the scratch was recorded every 24 h. Caspase-3 activity was detected by Caspase-3 activity assay kit (C1073S, Beyotime) 24 h after transfection. ..

    Transferring:

    Article Title: XopA: a novel type III secretion system effector in Xenorhabdus that modulates host cell responses through apoptosis, autophagy, and immune evasion
    Article Snippet: In the determination of cell activity, the cells were detected by the MTT kit (C0009S, Beyotime) after transfection for 24 h and 48 h. When the cell clone formation was determined, the cells were continuously cultured for 14 days after transfection, fixed with ethanol, and counted after crystal violet staining. .. For scratch repair, the transfected cells were subjected to a 10 μL sterile pipette tip to form an equal-width scratch, and the width of the scratch was recorded every 24 h. Caspase-3 activity was detected by Caspase-3 activity assay kit (C1073S, Beyotime) 24 h after transfection. ..



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    Beyotime caspase 3 level measurement caspase 3 activity assay kit
    Glibenclamide disrupted SUR1-PARP1 interaction to restore DNA repair and attenuate apoptosis and inflammation in HBE cells (A) Schematic diagram of HBE cells with different treatments, followed by RNA sequencing analysis. Groups: control, 20 ng/mL; TNF-α, 100 μmol/L; glibenclamide plus TNF-α. n = 2 per group. (B) Venn diagram of differentially expressed genes. (C) GO and KEGG enrichment analyses of 280 genes in the intersection shown in (B). (D) RT-qPCR analysis of HBE cells with different treatments as indicated. (E) Co-immunoprecipitation assay in HBE cells transfected with FLAG-SUR1 plasmids and treated with 20 ng/mL TNF-α or 100 μmol/L glibenclamide as indicated. L.E., long exposure. (F) HBE cells were treated as in (E), then subjected to cytoplasmic and nuclear protein fractionation followed by western blotting. Cyto, cytoplasm; Nu, nucleus. (G) Western blot analysis of HBE cells pretreated with 100 μmol/L glibenclamide for 30 min followed by TNF-α or LPS co-treatment for 1 h. (H–J) ROS <t>production,</t> <t>caspase-3</t> activity, and apoptosis in HBE cells under indicated treatments. (K–M) HBE cells were pretreated with 100 μmol/L glibenclamide, 5 μmol/L olaparib, or their combination for 24 h, followed by 20 ng/mL TNF-α stimulation, and subjected to western blotting, caspase-3 activity assay, and apoptosis analysis by flow cytometry. Gli, glibenclamide. Data are presented as mean ± SD ( n = 3). ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. GO and KEGG enrichment analyses in (C) were performed using a hypergeometric test with false discovery rate (FDR) correction. Data in (D) and (G–M) were analyzed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Representative images are shown.
    Caspase 3 Level Measurement Caspase 3 Activity Assay Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Beyotime caspase 3 activity kit
    Glibenclamide disrupted SUR1-PARP1 interaction to restore DNA repair and attenuate apoptosis and inflammation in HBE cells (A) Schematic diagram of HBE cells with different treatments, followed by RNA sequencing analysis. Groups: control, 20 ng/mL; TNF-α, 100 μmol/L; glibenclamide plus TNF-α. n = 2 per group. (B) Venn diagram of differentially expressed genes. (C) GO and KEGG enrichment analyses of 280 genes in the intersection shown in (B). (D) RT-qPCR analysis of HBE cells with different treatments as indicated. (E) Co-immunoprecipitation assay in HBE cells transfected with FLAG-SUR1 plasmids and treated with 20 ng/mL TNF-α or 100 μmol/L glibenclamide as indicated. L.E., long exposure. (F) HBE cells were treated as in (E), then subjected to cytoplasmic and nuclear protein fractionation followed by western blotting. Cyto, cytoplasm; Nu, nucleus. (G) Western blot analysis of HBE cells pretreated with 100 μmol/L glibenclamide for 30 min followed by TNF-α or LPS co-treatment for 1 h. (H–J) ROS <t>production,</t> <t>caspase-3</t> activity, and apoptosis in HBE cells under indicated treatments. (K–M) HBE cells were pretreated with 100 μmol/L glibenclamide, 5 μmol/L olaparib, or their combination for 24 h, followed by 20 ng/mL TNF-α stimulation, and subjected to western blotting, caspase-3 activity assay, and apoptosis analysis by flow cytometry. Gli, glibenclamide. Data are presented as mean ± SD ( n = 3). ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. GO and KEGG enrichment analyses in (C) were performed using a hypergeometric test with false discovery rate (FDR) correction. Data in (D) and (G–M) were analyzed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Representative images are shown.
    Caspase 3 Activity Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/caspase+3+activity+assay+kit/Caspase+3+Activity+Assay+Kit/pm41985289-59-9-45
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    Glibenclamide disrupted SUR1-PARP1 interaction to restore DNA repair and attenuate apoptosis and inflammation in HBE cells (A) Schematic diagram of HBE cells with different treatments, followed by RNA sequencing analysis. Groups: control, 20 ng/mL; TNF-α, 100 μmol/L; glibenclamide plus TNF-α. n = 2 per group. (B) Venn diagram of differentially expressed genes. (C) GO and KEGG enrichment analyses of 280 genes in the intersection shown in (B). (D) RT-qPCR analysis of HBE cells with different treatments as indicated. (E) Co-immunoprecipitation assay in HBE cells transfected with FLAG-SUR1 plasmids and treated with 20 ng/mL TNF-α or 100 μmol/L glibenclamide as indicated. L.E., long exposure. (F) HBE cells were treated as in (E), then subjected to cytoplasmic and nuclear protein fractionation followed by western blotting. Cyto, cytoplasm; Nu, nucleus. (G) Western blot analysis of HBE cells pretreated with 100 μmol/L glibenclamide for 30 min followed by TNF-α or LPS co-treatment for 1 h. (H–J) ROS <t>production,</t> <t>caspase-3</t> activity, and apoptosis in HBE cells under indicated treatments. (K–M) HBE cells were pretreated with 100 μmol/L glibenclamide, 5 μmol/L olaparib, or their combination for 24 h, followed by 20 ng/mL TNF-α stimulation, and subjected to western blotting, caspase-3 activity assay, and apoptosis analysis by flow cytometry. Gli, glibenclamide. Data are presented as mean ± SD ( n = 3). ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. GO and KEGG enrichment analyses in (C) were performed using a hypergeometric test with false discovery rate (FDR) correction. Data in (D) and (G–M) were analyzed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Representative images are shown.
    Caspase 3, supplied by Beyotime, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Beyotime caspase 3 enzyme activity assay kit
    The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and <t>Caspase</t> <t>3</t> in E.tenella host cells.
    Caspase 3 Enzyme Activity Assay Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Glibenclamide disrupted SUR1-PARP1 interaction to restore DNA repair and attenuate apoptosis and inflammation in HBE cells (A) Schematic diagram of HBE cells with different treatments, followed by RNA sequencing analysis. Groups: control, 20 ng/mL; TNF-α, 100 μmol/L; glibenclamide plus TNF-α. n = 2 per group. (B) Venn diagram of differentially expressed genes. (C) GO and KEGG enrichment analyses of 280 genes in the intersection shown in (B). (D) RT-qPCR analysis of HBE cells with different treatments as indicated. (E) Co-immunoprecipitation assay in HBE cells transfected with FLAG-SUR1 plasmids and treated with 20 ng/mL TNF-α or 100 μmol/L glibenclamide as indicated. L.E., long exposure. (F) HBE cells were treated as in (E), then subjected to cytoplasmic and nuclear protein fractionation followed by western blotting. Cyto, cytoplasm; Nu, nucleus. (G) Western blot analysis of HBE cells pretreated with 100 μmol/L glibenclamide for 30 min followed by TNF-α or LPS co-treatment for 1 h. (H–J) ROS production, caspase-3 activity, and apoptosis in HBE cells under indicated treatments. (K–M) HBE cells were pretreated with 100 μmol/L glibenclamide, 5 μmol/L olaparib, or their combination for 24 h, followed by 20 ng/mL TNF-α stimulation, and subjected to western blotting, caspase-3 activity assay, and apoptosis analysis by flow cytometry. Gli, glibenclamide. Data are presented as mean ± SD ( n = 3). ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. GO and KEGG enrichment analyses in (C) were performed using a hypergeometric test with false discovery rate (FDR) correction. Data in (D) and (G–M) were analyzed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Representative images are shown.

    Journal: iScience

    Article Title: Sulfonylurea receptor 1 deficiency alleviates acute lung injury by activating PARP1 in epithelial cells

    doi: 10.1016/j.isci.2026.117627

    Figure Lengend Snippet: Glibenclamide disrupted SUR1-PARP1 interaction to restore DNA repair and attenuate apoptosis and inflammation in HBE cells (A) Schematic diagram of HBE cells with different treatments, followed by RNA sequencing analysis. Groups: control, 20 ng/mL; TNF-α, 100 μmol/L; glibenclamide plus TNF-α. n = 2 per group. (B) Venn diagram of differentially expressed genes. (C) GO and KEGG enrichment analyses of 280 genes in the intersection shown in (B). (D) RT-qPCR analysis of HBE cells with different treatments as indicated. (E) Co-immunoprecipitation assay in HBE cells transfected with FLAG-SUR1 plasmids and treated with 20 ng/mL TNF-α or 100 μmol/L glibenclamide as indicated. L.E., long exposure. (F) HBE cells were treated as in (E), then subjected to cytoplasmic and nuclear protein fractionation followed by western blotting. Cyto, cytoplasm; Nu, nucleus. (G) Western blot analysis of HBE cells pretreated with 100 μmol/L glibenclamide for 30 min followed by TNF-α or LPS co-treatment for 1 h. (H–J) ROS production, caspase-3 activity, and apoptosis in HBE cells under indicated treatments. (K–M) HBE cells were pretreated with 100 μmol/L glibenclamide, 5 μmol/L olaparib, or their combination for 24 h, followed by 20 ng/mL TNF-α stimulation, and subjected to western blotting, caspase-3 activity assay, and apoptosis analysis by flow cytometry. Gli, glibenclamide. Data are presented as mean ± SD ( n = 3). ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001. GO and KEGG enrichment analyses in (C) were performed using a hypergeometric test with false discovery rate (FDR) correction. Data in (D) and (G–M) were analyzed using one-way ANOVA followed by Tukey’s multiple-comparisons test. Representative images are shown.

    Article Snippet: Caspase 3 Activity Assay Kit , Beyotime Biotechnology , Cat# C1115.

    Techniques: RNA Sequencing, Analysis, Control, Quantitative RT-PCR, Co-Immunoprecipitation Assay, Transfection, Fractionation, Western Blot, Activity Assay, Caspase-3 Activity Assay, Flow Cytometry

    Journal: iScience

    Article Title: Sulfonylurea receptor 1 deficiency alleviates acute lung injury by activating PARP1 in epithelial cells

    doi: 10.1016/j.isci.2026.117627

    Figure Lengend Snippet:

    Article Snippet: Caspase 3 Activity Assay Kit , Beyotime Biotechnology , Cat# C1115.

    Techniques: Cell-Signaling, Recombinant, Transfection, Caspase-3 Activity Assay, Protein Extraction, Knock-Out, Sequencing, Control, Plasmid Preparation, Software, Analysis

    The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Article Snippet: According to the instructions of the Caspase-3 Enzyme Activity Assay Kit (Beyotime, Shanghai, China), cells from each group were lysed for 15 min on ice using lysis buffer.

    Techniques: Expressing

    The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Article Snippet: According to the instructions of the Caspase-3 Enzyme Activity Assay Kit (Beyotime, Shanghai, China), cells from each group were lysed for 15 min on ice using lysis buffer.

    Techniques: Activity Assay

    Effect of Et MIC2 on E.tenella infection rate and Caspase 3 Activity through ITGAV.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: Effect of Et MIC2 on E.tenella infection rate and Caspase 3 Activity through ITGAV.

    Article Snippet: According to the instructions of the Caspase-3 Enzyme Activity Assay Kit (Beyotime, Shanghai, China), cells from each group were lysed for 15 min on ice using lysis buffer.

    Techniques: Infection, Activity Assay