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annexin v fitc propidium iodide pi dual staining kit  (Keygen Biotech)

 
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    Structured Review

    Keygen Biotech annexin v fitc propidium iodide pi dual staining kit
    BS combined with DAC showed enhanced effects in inhibiting the survival of lung cancer cells. A549 and H1299 cells were treated with BS, DAC, or BS + DAC (3:1 for A549 [BS-5 μM, DAC-1.67 μM] and 2:1 for H1299 [BS-5 μM, DAC-2.5 μM]) for 48 h, followed by <t>Annexin</t> V-PI staining. The results of total apoptosis (including both early and late apoptotic populations) are shown as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001, compared with each indicated group by one-way ANOVA followed by Tukey’s post hoc test analysis ( n = 3).
    Annexin V Fitc Propidium Iodide Pi Dual Staining Kit, supplied by Keygen Biotech, 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/annexin+v+fitc+propidium+iodide+pi+dual+staining+kit/assay+kit+luciferase/pmc13153144-79-12-20
    Average 86 stars, based on 1 article reviews
    annexin v fitc propidium iodide pi dual staining kit - by Bioz Stars, 2026-11
    86/100 stars

    Images

    1) Product Images from "The combined inhibitory effect of butaselen and decitabine against lung cancer cells"

    Article Title: The combined inhibitory effect of butaselen and decitabine against lung cancer cells

    Journal: Scientific Reports

    doi: 10.1038/s41598-026-45054-7

    BS combined with DAC showed enhanced effects in inhibiting the survival of lung cancer cells. A549 and H1299 cells were treated with BS, DAC, or BS + DAC (3:1 for A549 [BS-5 μM, DAC-1.67 μM] and 2:1 for H1299 [BS-5 μM, DAC-2.5 μM]) for 48 h, followed by Annexin V-PI staining. The results of total apoptosis (including both early and late apoptotic populations) are shown as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001, compared with each indicated group by one-way ANOVA followed by Tukey’s post hoc test analysis ( n = 3).
    Figure Legend Snippet: BS combined with DAC showed enhanced effects in inhibiting the survival of lung cancer cells. A549 and H1299 cells were treated with BS, DAC, or BS + DAC (3:1 for A549 [BS-5 μM, DAC-1.67 μM] and 2:1 for H1299 [BS-5 μM, DAC-2.5 μM]) for 48 h, followed by Annexin V-PI staining. The results of total apoptosis (including both early and late apoptotic populations) are shown as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001, compared with each indicated group by one-way ANOVA followed by Tukey’s post hoc test analysis ( n = 3).

    Techniques Used: Staining

    Related Articles

    Apoptosis Assay:

    Article Title: The novel thioredoxin reductase inhibitor butaselen suppresses lung cancer by inducing oxidative stress
    Article Snippet: .. The cells were collected, and the apoptosis assay was conducted using the Annexin V-FITC/ propidium iodide (PI) Dual Staining Kit (KeyGEN) as instructed by the manufacturer and described previously [ ]. ..

    Article Title: The combined inhibitory effect of butaselen and decitabine against lung cancer cells.
    Article Snippet: .. The cells were collected, and the apoptosis assay was conducted using the Annexin V-FITC/ propidium iodide (PI) Dual Staining Kit (KeyGEN) as instructed by the manufacturer and described previously 28. ..

    Article Title: The combined inhibitory effect of butaselen and decitabine against lung cancer cells
    Article Snippet: .. The cells were collected, and the apoptosis assay was conducted using the Annexin V-FITC/ propidium iodide (PI) Dual Staining Kit (KeyGEN) as instructed by the manufacturer and described previously . ..

    Article Title: The novel thioredoxin reductase inhibitor butaselen suppresses lung cancer by inducing oxidative stress.
    Article Snippet: .. The cells were collected, and the apoptosis assay was conducted using the Annexin V-FITC/ propidium iodide (PI) Dual Staining Kit (KeyGEN) as instructed by the manufacturer and described previously [25]. ..

    Staining:

    Article Title: The novel thioredoxin reductase inhibitor butaselen suppresses lung cancer by inducing oxidative stress
    Article Snippet: .. The cells were collected, and the apoptosis assay was conducted using the Annexin V-FITC/ propidium iodide (PI) Dual Staining Kit (KeyGEN) as instructed by the manufacturer and described previously [ ]. ..

    Article Title: The combined inhibitory effect of butaselen and decitabine against lung cancer cells.
    Article Snippet: .. The cells were collected, and the apoptosis assay was conducted using the Annexin V-FITC/ propidium iodide (PI) Dual Staining Kit (KeyGEN) as instructed by the manufacturer and described previously 28. ..

    Article Title: The combined inhibitory effect of butaselen and decitabine against lung cancer cells
    Article Snippet: .. The cells were collected, and the apoptosis assay was conducted using the Annexin V-FITC/ propidium iodide (PI) Dual Staining Kit (KeyGEN) as instructed by the manufacturer and described previously . ..

    Article Title: The novel thioredoxin reductase inhibitor butaselen suppresses lung cancer by inducing oxidative stress.
    Article Snippet: .. The cells were collected, and the apoptosis assay was conducted using the Annexin V-FITC/ propidium iodide (PI) Dual Staining Kit (KeyGEN) as instructed by the manufacturer and described previously [25]. ..



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    Piperine induces the apoptosis of SNU-16 cells. ( A ) SNU-16 cells were exposed to piperine (50, 100, 150 μM) for 24 h. Percentage of cell apoptosis was determined by annexin V/PI staining and flow cytometry. ( B ) The apoptotic rates of SNU-16 cells induced by piperine. Data are presented as the mean±SD of at least 3 independent experiments, * P <0.05, ** P <0.01 and *** P <0.001 compared with control cells.
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    Image Search Results


    BS combined with DAC showed enhanced effects in inhibiting the survival of lung cancer cells. A549 and H1299 cells were treated with BS, DAC, or BS + DAC (3:1 for A549 [BS-5 μM, DAC-1.67 μM] and 2:1 for H1299 [BS-5 μM, DAC-2.5 μM]) for 48 h, followed by Annexin V-PI staining. The results of total apoptosis (including both early and late apoptotic populations) are shown as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001, compared with each indicated group by one-way ANOVA followed by Tukey’s post hoc test analysis ( n = 3).

    Journal: Scientific Reports

    Article Title: The combined inhibitory effect of butaselen and decitabine against lung cancer cells

    doi: 10.1038/s41598-026-45054-7

    Figure Lengend Snippet: BS combined with DAC showed enhanced effects in inhibiting the survival of lung cancer cells. A549 and H1299 cells were treated with BS, DAC, or BS + DAC (3:1 for A549 [BS-5 μM, DAC-1.67 μM] and 2:1 for H1299 [BS-5 μM, DAC-2.5 μM]) for 48 h, followed by Annexin V-PI staining. The results of total apoptosis (including both early and late apoptotic populations) are shown as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001, compared with each indicated group by one-way ANOVA followed by Tukey’s post hoc test analysis ( n = 3).

    Article Snippet: The cells were collected, and the apoptosis assay was conducted using the Annexin V-FITC/ propidium iodide (PI) Dual Staining Kit (KeyGEN) as instructed by the manufacturer and described previously .

    Techniques: Staining

    Piperine induces the apoptosis of SNU-16 cells. ( A ) SNU-16 cells were exposed to piperine (50, 100, 150 μM) for 24 h. Percentage of cell apoptosis was determined by annexin V/PI staining and flow cytometry. ( B ) The apoptotic rates of SNU-16 cells induced by piperine. Data are presented as the mean±SD of at least 3 independent experiments, * P <0.05, ** P <0.01 and *** P <0.001 compared with control cells.

    Journal: Medical Science Monitor : International Medical Journal of Experimental and Clinical Research

    Article Title: Piperine Inhibits Cell Proliferation and Induces Apoptosis of Human Gastric Cancer Cells by Downregulating Phosphatidylinositol 3-Kinase (PI3K)/Akt Pathway

    doi: 10.12659/MSM.928403

    Figure Lengend Snippet: Piperine induces the apoptosis of SNU-16 cells. ( A ) SNU-16 cells were exposed to piperine (50, 100, 150 μM) for 24 h. Percentage of cell apoptosis was determined by annexin V/PI staining and flow cytometry. ( B ) The apoptotic rates of SNU-16 cells induced by piperine. Data are presented as the mean±SD of at least 3 independent experiments, * P <0.05, ** P <0.01 and *** P <0.001 compared with control cells.

    Article Snippet: After that, the cell pellet was resuspended in 500 μl binding buffer and the apoptosis rate was examined by annexin V-FITC/PI (fluorescein isothiocyanate/propidium iodide) dual staining apoptosis detection kit (Nanjing KeyGEN Biotech.

    Techniques: Staining, Flow Cytometry

    The efficacy of Akt activator (SC79) on piperine-induced apoptosis. SNU-16 cells were determined after treatment with piperine for 24 h in the presence or absence of SC79 (10 μM). ( A ) Apoptosis detection with annexin V/PI double staining in different groups by flow cytometry. ( B ) Column bar graph of mean cell florescence for early apoptotic, late apoptotic, and total apoptotic cells. ( C ) Expression of pAkt, Akt, cleaved caspase3, and cleaved PARP proteins in the presence or absence of SC79. ( D ) Quantification of pAkt, Akt, cleaved caspase3, and cleaved PARP proteins. ( E ) Expression of Bcl-2 and Bax proteins after piperine and/or SC79 treatment. ( F ) Quantification of Bcl-2 and Bax proteins. The Bcl-2/Bax ratio was significantly upregulated in the presence of SC79. Data are presented as the mean±SD of at least 3 independent experiments, * P <0.05, ** P <0.01 and *** P <0.001 compared with control cells; # P <0.05, ## P <0.01 and ### P <0.001 compared with the piperine alone group.

    Journal: Medical Science Monitor : International Medical Journal of Experimental and Clinical Research

    Article Title: Piperine Inhibits Cell Proliferation and Induces Apoptosis of Human Gastric Cancer Cells by Downregulating Phosphatidylinositol 3-Kinase (PI3K)/Akt Pathway

    doi: 10.12659/MSM.928403

    Figure Lengend Snippet: The efficacy of Akt activator (SC79) on piperine-induced apoptosis. SNU-16 cells were determined after treatment with piperine for 24 h in the presence or absence of SC79 (10 μM). ( A ) Apoptosis detection with annexin V/PI double staining in different groups by flow cytometry. ( B ) Column bar graph of mean cell florescence for early apoptotic, late apoptotic, and total apoptotic cells. ( C ) Expression of pAkt, Akt, cleaved caspase3, and cleaved PARP proteins in the presence or absence of SC79. ( D ) Quantification of pAkt, Akt, cleaved caspase3, and cleaved PARP proteins. ( E ) Expression of Bcl-2 and Bax proteins after piperine and/or SC79 treatment. ( F ) Quantification of Bcl-2 and Bax proteins. The Bcl-2/Bax ratio was significantly upregulated in the presence of SC79. Data are presented as the mean±SD of at least 3 independent experiments, * P <0.05, ** P <0.01 and *** P <0.001 compared with control cells; # P <0.05, ## P <0.01 and ### P <0.001 compared with the piperine alone group.

    Article Snippet: After that, the cell pellet was resuspended in 500 μl binding buffer and the apoptosis rate was examined by annexin V-FITC/PI (fluorescein isothiocyanate/propidium iodide) dual staining apoptosis detection kit (Nanjing KeyGEN Biotech.

    Techniques: Double Staining, Flow Cytometry, Expressing