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BPA exposure induces mitochondrial dysfunction, mitigated by NaOx or AC45594 HESC were treated with CTL or 50 nM BPA for 3 days, followed by 3-day treatment with vehicle, NaOx (20 mM), or AC45594 (5 μM). (A) Intracellular ATP. (B) Mitochondrial DNA copy number. (C) Mitochondrial membrane potential (ΔΨm). (D) Representative TMRE images. <t>(E)</t> <t>Caspase-3</t> activity. (F) Apoptosis rate. n means number of independent repeats, n = 5. ∗, p < 0.05 vs. CTL(3d)+CTL(3d)/VEH; ¶, p < 0.05 vs. BPA(3d) + CTL(3d)/VEH. Data are presented as mean ± SD.
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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.
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Beyotime greennuctm live cell caspase 3 activity assay kit
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Novus Biologicals nbp2 54838 100 assays
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Novus Biologicals caspase 3 activity assay kit colorimetric
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Elabscience Biotechnology caspase 3 7 activity assay kit
Effect of curcumin, spanlastics-free, curcumin nanocrystals, and curcumin spanlastics on <t>Caspase</t> <t>3</t> activity using Caspase 3 Activity Assay Kit (Colorimetric) on the IC50 concentration detected by MTT viability test (IC50 = 240.85, 67.7, 47.83, and 37.18 µg/mL µg/mL, respectively, incubation for 48 h). Data were expressed as mean ± SD ( n = 3). a means significant versus the control group and b means significant versus the curcumin group. Control: cancer cell without any treatments. Each group differed significantly from the others at p ≤ 0.05
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BPA exposure induces mitochondrial dysfunction, mitigated by NaOx or AC45594 HESC were treated with CTL or 50 nM BPA for 3 days, followed by 3-day treatment with vehicle, NaOx (20 mM), or AC45594 (5 μM). (A) Intracellular ATP. (B) Mitochondrial DNA copy number. (C) Mitochondrial membrane potential (ΔΨm). (D) Representative TMRE images. (E) Caspase-3 activity. (F) Apoptosis rate. n means number of independent repeats, n = 5. ∗, p < 0.05 vs. CTL(3d)+CTL(3d)/VEH; ¶, p < 0.05 vs. BPA(3d) + CTL(3d)/VEH. Data are presented as mean ± SD.

Journal: iScience

Article Title: Prenatal bisphenol A exposure reprograms SF1-lactylation pathways to promote endometriosis susceptibility

doi: 10.1016/j.isci.2026.115608

Figure Lengend Snippet: BPA exposure induces mitochondrial dysfunction, mitigated by NaOx or AC45594 HESC were treated with CTL or 50 nM BPA for 3 days, followed by 3-day treatment with vehicle, NaOx (20 mM), or AC45594 (5 μM). (A) Intracellular ATP. (B) Mitochondrial DNA copy number. (C) Mitochondrial membrane potential (ΔΨm). (D) Representative TMRE images. (E) Caspase-3 activity. (F) Apoptosis rate. n means number of independent repeats, n = 5. ∗, p < 0.05 vs. CTL(3d)+CTL(3d)/VEH; ¶, p < 0.05 vs. BPA(3d) + CTL(3d)/VEH. Data are presented as mean ± SD.

Article Snippet: ApoAlert Caspase-3 Activity Kit , Clontech , Cat# 630216.

Techniques: Membrane, Activity Assay

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

The content of Caspase-3 and ROS in cells treated with Zn alloy extract. A–B: The content of Caspase-3 ( A ) ROS ( B ) and in L929 cells treated with different Zn alloy extract. C-D: The content of Caspase-3 ( C ) ROS ( D ) and in RAW264.7 cells treated with Zn alloy extract. Magnification: 40 × , Scale bar: 10 μm.

Journal: Bioactive Materials

Article Title: Degradation behavior and biological properties of a novel biodegradable zinc alloy biliary stent

doi: 10.1016/j.bioactmat.2025.12.022

Figure Lengend Snippet: The content of Caspase-3 and ROS in cells treated with Zn alloy extract. A–B: The content of Caspase-3 ( A ) ROS ( B ) and in L929 cells treated with different Zn alloy extract. C-D: The content of Caspase-3 ( C ) ROS ( D ) and in RAW264.7 cells treated with Zn alloy extract. Magnification: 40 × , Scale bar: 10 μm.

Article Snippet: Reactive Oxygen Species Assay Kit and GreenNucTM Live Cell Caspase-3 Activity Assay Kit were purchased from Beyotime (China).

Techniques:

Effect of curcumin, spanlastics-free, curcumin nanocrystals, and curcumin spanlastics on Caspase 3 activity using Caspase 3 Activity Assay Kit (Colorimetric) on the IC50 concentration detected by MTT viability test (IC50 = 240.85, 67.7, 47.83, and 37.18 µg/mL µg/mL, respectively, incubation for 48 h). Data were expressed as mean ± SD ( n = 3). a means significant versus the control group and b means significant versus the curcumin group. Control: cancer cell without any treatments. Each group differed significantly from the others at p ≤ 0.05

Journal: BMC Biotechnology

Article Title: An assessment of curcumin, curcumin spanlastics nanoparticles, and curcumin nanocrystals as possible drug delivery systems with antimicrobial, antioxidant, and antitumor activities

doi: 10.1186/s12896-026-01153-x

Figure Lengend Snippet: Effect of curcumin, spanlastics-free, curcumin nanocrystals, and curcumin spanlastics on Caspase 3 activity using Caspase 3 Activity Assay Kit (Colorimetric) on the IC50 concentration detected by MTT viability test (IC50 = 240.85, 67.7, 47.83, and 37.18 µg/mL µg/mL, respectively, incubation for 48 h). Data were expressed as mean ± SD ( n = 3). a means significant versus the control group and b means significant versus the curcumin group. Control: cancer cell without any treatments. Each group differed significantly from the others at p ≤ 0.05

Article Snippet: Caspase 3 Activity was estimated through Caspase 3 Activity Assay Kit (Colorimetric), NBP2-54838-100 Assays, Novus Biologicals LLC, a Bio-Techne Brand, according to manufacturer protocol through HiPo MPP-96 Microplate Photometer and 3D-IW8 Inteliwasher (Biosan).

Techniques: Activity Assay, Caspase-3 Activity Assay, Concentration Assay, Incubation, Control