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annexin v apc pi staining kit  (Elabscience Biotechnology)


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    Elabscience Biotechnology annexin v apc pi staining kit
    Annexin V Apc Pi Staining Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 208 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/annexin v apc pi staining kit/product/Elabscience Biotechnology
    Average 96 stars, based on 208 article reviews
    annexin v apc pi staining kit - by Bioz Stars, 2026-06
    96/100 stars

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    Nanjing KeyGen Biotech Co Ltd annexin v-apc/pi double staining apoptosis detection kit
    ETHE1 knockdown promotes CAG cell <t>apoptosis.</t> (A) Flow cytometric analysis of apoptosis. (B) Apoptosis of gastric adenocarcinoma cells was detected by TUNEL staining. Scale bar, 50 µm. (C) Caspase-3 and (D) caspase-9 activity was detected using kits. **P<0.01, ***P<0.001. Ctrl, control; sh, short hairpin.
    Annexin V Apc/Pi Double Staining Apoptosis Detection Kit, supplied by Nanjing KeyGen Biotech Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Effect of ITPKA overexpression on the functional characteristics of GBM cells. Flow cytometry analysis (A, B) shows the effect of upregulated ITPKA expression on the cell cycle progression of U251-MG and T98G cells; (C, D) evaluates the effect of upregulated ITPKA expression on the apoptosis level of the two indicated cell lines. All experimental data are presented as mean ± standard deviation (SD) from six independent repeated experiments, and Student’s t-test was used for statistical analysis. Data annotation: ns: not significant; *p < 0.05, ****p < 0.0001.

    Journal: Frontiers in Oncology

    Article Title: ITPKA suppresses glioma progression and predicts patient prognosis

    doi: 10.3389/fonc.2026.1802857

    Figure Lengend Snippet: Effect of ITPKA overexpression on the functional characteristics of GBM cells. Flow cytometry analysis (A, B) shows the effect of upregulated ITPKA expression on the cell cycle progression of U251-MG and T98G cells; (C, D) evaluates the effect of upregulated ITPKA expression on the apoptosis level of the two indicated cell lines. All experimental data are presented as mean ± standard deviation (SD) from six independent repeated experiments, and Student’s t-test was used for statistical analysis. Data annotation: ns: not significant; *p < 0.05, ****p < 0.0001.

    Article Snippet: A total of 5×10 5 stably transfected U251-MG and T98G cells were centrifuged, after which apoptosis detection was performed using the Annexin V-APC/PI Double Staining Apoptosis Detection Kit (KGA1107-100; Keygen Biotech, Nanjing, China).

    Techniques: Over Expression, Functional Assay, Flow Cytometry, Expressing, Standard Deviation

    Effect of ITPKA knockdown on the functional characteristics of GBM cells. Flow cytometry analysis (A, B) shows the effect of downregulated ITPKA expression on the cell cycle progression of U251-MG and T98G cells; (C, D) evaluates the effect of downregulated ITPKA expression on the apoptosis level of the two indicated cell lines. All experimental data are presented as mean ± standard deviation (SD) from six independent repeated experiments, and Student’s t-test was used for statistical analysis. Data annotation: ns: not significant; *p < 0.05, **p < 0.01, ****p < 0.0001.

    Journal: Frontiers in Oncology

    Article Title: ITPKA suppresses glioma progression and predicts patient prognosis

    doi: 10.3389/fonc.2026.1802857

    Figure Lengend Snippet: Effect of ITPKA knockdown on the functional characteristics of GBM cells. Flow cytometry analysis (A, B) shows the effect of downregulated ITPKA expression on the cell cycle progression of U251-MG and T98G cells; (C, D) evaluates the effect of downregulated ITPKA expression on the apoptosis level of the two indicated cell lines. All experimental data are presented as mean ± standard deviation (SD) from six independent repeated experiments, and Student’s t-test was used for statistical analysis. Data annotation: ns: not significant; *p < 0.05, **p < 0.01, ****p < 0.0001.

    Article Snippet: A total of 5×10 5 stably transfected U251-MG and T98G cells were centrifuged, after which apoptosis detection was performed using the Annexin V-APC/PI Double Staining Apoptosis Detection Kit (KGA1107-100; Keygen Biotech, Nanjing, China).

    Techniques: Knockdown, Functional Assay, Flow Cytometry, Expressing, Standard Deviation

    ETHE1 knockdown promotes CAG cell apoptosis. (A) Flow cytometric analysis of apoptosis. (B) Apoptosis of gastric adenocarcinoma cells was detected by TUNEL staining. Scale bar, 50 µm. (C) Caspase-3 and (D) caspase-9 activity was detected using kits. **P<0.01, ***P<0.001. Ctrl, control; sh, short hairpin.

    Journal: Oncology Letters

    Article Title: Targeting ETHE1 inhibits tumorigenesis in vitro and in vivo by preventing aerobic glycolysis in gastric adenocarcinoma cells

    doi: 10.3892/ol.2025.15032

    Figure Lengend Snippet: ETHE1 knockdown promotes CAG cell apoptosis. (A) Flow cytometric analysis of apoptosis. (B) Apoptosis of gastric adenocarcinoma cells was detected by TUNEL staining. Scale bar, 50 µm. (C) Caspase-3 and (D) caspase-9 activity was detected using kits. **P<0.01, ***P<0.001. Ctrl, control; sh, short hairpin.

    Article Snippet: Cell cycle distribution and apoptosis were analyzed using a flow cytometer (NovoCyte-D2060R; Agilent Technologies, Inc.), and a Cell Cycle and Apoptosis Analysis Kit (BioSharp Life Sciences) or an Annexin V-APC/PI double staining apoptosis detection kit (Nanjing KeyGen Biotech Co., Ltd.), respectively, according to the manufacturers' protocols.

    Techniques: Knockdown, TUNEL Assay, Staining, Activity Assay, Control

    BALB/c nude mice received subcutaneous injections of stabilized infected NCI-N87 cells to induce tumor formation in vivo . (A) Tumor tissue images, tumor growth curve and tumor weight. (B) Representative immunohistochemical staining images of Ki67 and ETHE1. (C) Apoptosis in gastric adenocarcinoma tissue was detected by TUNEL staining. Scale bar, 100 µm. *P<0.05, **P<0.01 and ***P<0.001 vs. Ctrl. Ctrl, control; ETHEI, ethylmalonic encephalopathy protein 1; sh, short hairpin.

    Journal: Oncology Letters

    Article Title: Targeting ETHE1 inhibits tumorigenesis in vitro and in vivo by preventing aerobic glycolysis in gastric adenocarcinoma cells

    doi: 10.3892/ol.2025.15032

    Figure Lengend Snippet: BALB/c nude mice received subcutaneous injections of stabilized infected NCI-N87 cells to induce tumor formation in vivo . (A) Tumor tissue images, tumor growth curve and tumor weight. (B) Representative immunohistochemical staining images of Ki67 and ETHE1. (C) Apoptosis in gastric adenocarcinoma tissue was detected by TUNEL staining. Scale bar, 100 µm. *P<0.05, **P<0.01 and ***P<0.001 vs. Ctrl. Ctrl, control; ETHEI, ethylmalonic encephalopathy protein 1; sh, short hairpin.

    Article Snippet: Cell cycle distribution and apoptosis were analyzed using a flow cytometer (NovoCyte-D2060R; Agilent Technologies, Inc.), and a Cell Cycle and Apoptosis Analysis Kit (BioSharp Life Sciences) or an Annexin V-APC/PI double staining apoptosis detection kit (Nanjing KeyGen Biotech Co., Ltd.), respectively, according to the manufacturers' protocols.

    Techniques: Infection, In Vivo, Immunohistochemical staining, Staining, TUNEL Assay, Control