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human hela cell line  (ATCC)


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    Structured Review

    ATCC human hela cell line
    Human Hela Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 16365 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+hela/HeLa/us12655474-990-1-12
    Average 99 stars, based on 16365 article reviews
    human hela cell line - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    other:

    Article Title: Robust calibration and quantification of FRET signals using multiplexed biosensor barcoding
    Article Snippet: Human: HeLa , ATCC , CCL-2; RRID:CVCL_0030.

    Cell Culture:

    Article Title: Olivetol induces a non-genotoxic nucleolar DNA damage response via membrane-dependent stress signaling
    Article Snippet: .. Human HeLa (ATCC® CCL-2TM), HEK293 (ATCC® CRL-1573TM), HAP1 and HCT116 (kindly provided by Dr. Nariman R Battulin, Institute of Cytology and Genetics SD RAS, Novosibirsk, Russia) cells were cultured in DMEM (PanEco) supplemented with 10% fetal bovine serum (FBS; HyClone/GE Healthcare) and penicillin/streptomycin. .. Human MV-4–11 (ATCC®CRL-9591TM), THP1 (ATCC®TIB-202TM), KG1 (ATCC®CRL-8031) and Kasumi-1 (ATCC®CRL-2724TM) were cultured in RPMI (PanEco) supplemented with 10% fetal bovine serum (FBS; HyClone/GE Healthcare) and penicillin/streptomycin.



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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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    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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    ATCC cell lines human hela atcc ccl
    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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    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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    ATCC human epithelial hela
    Characterization and optimization of the RPC enrichment process. (a) Dot blot analysis detecting BFP labeling of the RNA extracted from <t>HeLa</t> cells under 365 nm UV irradiation. SDS-PAGE characterization of enriched RBPs under different conditions, including 254 nm UV irradiation dose (b), BFP concentration (c), and 365 nm UV labeling time (d).
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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

    Characterization and optimization of the RPC enrichment process. (a) Dot blot analysis detecting BFP labeling of the RNA extracted from HeLa cells under 365 nm UV irradiation. SDS-PAGE characterization of enriched RBPs under different conditions, including 254 nm UV irradiation dose (b), BFP concentration (c), and 365 nm UV labeling time (d).

    Journal: RSC Advances

    Article Title: An approach for the systematic profiling of drug-induced remodeling of RNA–RBP (RNA-binding protein) interactions

    doi: 10.1039/d6ra00871b

    Figure Lengend Snippet: Characterization and optimization of the RPC enrichment process. (a) Dot blot analysis detecting BFP labeling of the RNA extracted from HeLa cells under 365 nm UV irradiation. SDS-PAGE characterization of enriched RBPs under different conditions, including 254 nm UV irradiation dose (b), BFP concentration (c), and 365 nm UV labeling time (d).

    Article Snippet: Human epithelial (HeLa), human colon cancer (HCT116) and human embryonic kidney (HEK293T) cell lines were obtained from the American Type Culture Collection (ATCC).

    Techniques: Dot Blot, Labeling, Irradiation, SDS Page, Concentration Assay