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human cervical cancer cells hela  (ATCC)


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    ATCC human cervical cancer cells hela
    Hypoxia increases expression of EZH2, H3K27me3 and survivin. (A) Immunoblots of WCEs <t>from</t> <t>U2OS,</t> <t>HeLa</t> and MRC5 lines cultured under normoxic or hypoxic environments (24 h). Blots were immunoprobed with anti-EZH2, anti-H3K27me3 and anti-survivin antibodies. Anti-Hif1a used to prove the hypoxic state had been induced, and anti-tubulin was used as a loading control. (B–D) Quantification of immunoblots represented in A from three independent experiments demonstrating that EZH2, H3K27me3 and survivin are all more abundant under hypoxia. Data presented are means±s.d. * P <0.05, ** P <0.01, *** P <0.001 (two-way ANOVA with Tukey's multiple comparisons post test).
    Human Cervical Cancer Cells Hela, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 10396 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 10396 article reviews
    human cervical cancer cells hela - by Bioz Stars, 2026-06
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    1) Product Images from "Interplay between nuclear survivin and the PRC2 complex and its impact on H3K27me3-directed transcriptional repression"

    Article Title: Interplay between nuclear survivin and the PRC2 complex and its impact on H3K27me3-directed transcriptional repression

    Journal: Journal of Cell Science

    doi: 10.1242/jcs.264572

    Hypoxia increases expression of EZH2, H3K27me3 and survivin. (A) Immunoblots of WCEs from U2OS, HeLa and MRC5 lines cultured under normoxic or hypoxic environments (24 h). Blots were immunoprobed with anti-EZH2, anti-H3K27me3 and anti-survivin antibodies. Anti-Hif1a used to prove the hypoxic state had been induced, and anti-tubulin was used as a loading control. (B–D) Quantification of immunoblots represented in A from three independent experiments demonstrating that EZH2, H3K27me3 and survivin are all more abundant under hypoxia. Data presented are means±s.d. * P <0.05, ** P <0.01, *** P <0.001 (two-way ANOVA with Tukey's multiple comparisons post test).
    Figure Legend Snippet: Hypoxia increases expression of EZH2, H3K27me3 and survivin. (A) Immunoblots of WCEs from U2OS, HeLa and MRC5 lines cultured under normoxic or hypoxic environments (24 h). Blots were immunoprobed with anti-EZH2, anti-H3K27me3 and anti-survivin antibodies. Anti-Hif1a used to prove the hypoxic state had been induced, and anti-tubulin was used as a loading control. (B–D) Quantification of immunoblots represented in A from three independent experiments demonstrating that EZH2, H3K27me3 and survivin are all more abundant under hypoxia. Data presented are means±s.d. * P <0.05, ** P <0.01, *** P <0.001 (two-way ANOVA with Tukey's multiple comparisons post test).

    Techniques Used: Expressing, Western Blot, Cell Culture, Control



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    human cervical cancer cells hela  (ATCC)
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    ATCC human cervical cancer cells hela
    Hypoxia increases expression of EZH2, H3K27me3 and survivin. (A) Immunoblots of WCEs <t>from</t> <t>U2OS,</t> <t>HeLa</t> and MRC5 lines cultured under normoxic or hypoxic environments (24 h). Blots were immunoprobed with anti-EZH2, anti-H3K27me3 and anti-survivin antibodies. Anti-Hif1a used to prove the hypoxic state had been induced, and anti-tubulin was used as a loading control. (B–D) Quantification of immunoblots represented in A from three independent experiments demonstrating that EZH2, H3K27me3 and survivin are all more abundant under hypoxia. Data presented are means±s.d. * P <0.05, ** P <0.01, *** P <0.001 (two-way ANOVA with Tukey's multiple comparisons post test).
    Human Cervical Cancer Cells Hela, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    hela cells  (CLS Cell Lines Service GmbH)
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    Hypoxia increases expression of EZH2, H3K27me3 and survivin. (A) Immunoblots of WCEs <t>from</t> <t>U2OS,</t> <t>HeLa</t> and MRC5 lines cultured under normoxic or hypoxic environments (24 h). Blots were immunoprobed with anti-EZH2, anti-H3K27me3 and anti-survivin antibodies. Anti-Hif1a used to prove the hypoxic state had been induced, and anti-tubulin was used as a loading control. (B–D) Quantification of immunoblots represented in A from three independent experiments demonstrating that EZH2, H3K27me3 and survivin are all more abundant under hypoxia. Data presented are means±s.d. * P <0.05, ** P <0.01, *** P <0.001 (two-way ANOVA with Tukey's multiple comparisons post test).
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    hela cells  (ATCC)
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    Hypoxia increases expression of EZH2, H3K27me3 and survivin. (A) Immunoblots of WCEs <t>from</t> <t>U2OS,</t> <t>HeLa</t> and MRC5 lines cultured under normoxic or hypoxic environments (24 h). Blots were immunoprobed with anti-EZH2, anti-H3K27me3 and anti-survivin antibodies. Anti-Hif1a used to prove the hypoxic state had been induced, and anti-tubulin was used as a loading control. (B–D) Quantification of immunoblots represented in A from three independent experiments demonstrating that EZH2, H3K27me3 and survivin are all more abundant under hypoxia. Data presented are means±s.d. * P <0.05, ** P <0.01, *** P <0.001 (two-way ANOVA with Tukey's multiple comparisons post test).
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    hela cells  (Korean Cell Line Bank)
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    Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of <t>HeLa</t> <t>cells</t> in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).
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    hela cells  (Thorlabs)
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    Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of <t>HeLa</t> <t>cells</t> in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).
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    Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of <t>HeLa</t> <t>cells</t> in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).
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    hela cell line  (Procell Inc)
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    Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of <t>HeLa</t> <t>cells</t> in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).
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    Image Search Results


    Hypoxia increases expression of EZH2, H3K27me3 and survivin. (A) Immunoblots of WCEs from U2OS, HeLa and MRC5 lines cultured under normoxic or hypoxic environments (24 h). Blots were immunoprobed with anti-EZH2, anti-H3K27me3 and anti-survivin antibodies. Anti-Hif1a used to prove the hypoxic state had been induced, and anti-tubulin was used as a loading control. (B–D) Quantification of immunoblots represented in A from three independent experiments demonstrating that EZH2, H3K27me3 and survivin are all more abundant under hypoxia. Data presented are means±s.d. * P <0.05, ** P <0.01, *** P <0.001 (two-way ANOVA with Tukey's multiple comparisons post test).

    Journal: Journal of Cell Science

    Article Title: Interplay between nuclear survivin and the PRC2 complex and its impact on H3K27me3-directed transcriptional repression

    doi: 10.1242/jcs.264572

    Figure Lengend Snippet: Hypoxia increases expression of EZH2, H3K27me3 and survivin. (A) Immunoblots of WCEs from U2OS, HeLa and MRC5 lines cultured under normoxic or hypoxic environments (24 h). Blots were immunoprobed with anti-EZH2, anti-H3K27me3 and anti-survivin antibodies. Anti-Hif1a used to prove the hypoxic state had been induced, and anti-tubulin was used as a loading control. (B–D) Quantification of immunoblots represented in A from three independent experiments demonstrating that EZH2, H3K27me3 and survivin are all more abundant under hypoxia. Data presented are means±s.d. * P <0.05, ** P <0.01, *** P <0.001 (two-way ANOVA with Tukey's multiple comparisons post test).

    Article Snippet: Human cervical cancer cells (HeLa), human bone osteosarcoma cells (U2OS), retinal pigment epithelial cells (RPE) and human breast cancer cells (MCF7) were originally from ATCC.

    Techniques: Expressing, Western Blot, Cell Culture, Control

    Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of HeLa cells in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).

    Journal: Chembiochem

    Article Title: Biomimetic Compartmentalization of Enzymes for Sustainable Coenzyme Recycling in Oxidative Photocatalysis

    doi: 10.1002/cbic.70381

    Figure Lengend Snippet: Cell protection of GDH@SiNPs against TiO2‐triggered ROS stress. (a) GDH@SiNPs can mitigate oxidative stress by continuously supplying NADH, which serves as a direct ROS scavenger. (b) Cell viability measured by CCK‐8 assay of HeLa cells in the presence of GDH@SiNPs and TiO2 nanoparticles under UV light irradiation. Effective cell protection of the GDH@SiNPs was achieved by enzymatic NADH production ( n = 4). Data are presented as mean ± SD ( n = 4). Statistical significance was determined by one‐way ANOVA followed by Tukey's post‐hoc test. Significant differences are indicated as **( p < 0.01), and ***( p < 0.001).

    Article Snippet: HeLa cells (Research Resource Identifier number: CVCL_0030) were obtained from Korea Cell Line Bank (KCLB No: 10 002, Seoul, Korea) and cultured in DMEM medium (Welgene, Gyeongsan, Korea) supplemented with 10% fetal bovine serum (FBS; qualified grade, Gibco, Thermo Fisher Scientific, Waltham, MA, USA).

    Techniques: CCK-8 Assay, Irradiation