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normal human bdec cells  (ATCC)


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    ATCC normal human bdec cells
    Normal Human Bdec Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 512 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/normal+human+bdec+cells/Primary+Bladder+Epithelial+Cells+(A%2FT%2FN)%3B+Normal%2C+Human/pmc11879136-47-40-52
    Average 99 stars, based on 512 article reviews
    normal human bdec cells - by Bioz Stars, 2026-10
    99/100 stars

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    other:

    Article Title: Sequestration of ribosomal subunits as inactive 80S by targeting eIF6 limits mitotic exit and cancer progression.
    Article Snippet: The human bladder cancer cell lines HT1376, HT1197, UM-UC-3 and TCCSUP were maintained in EMEM media with 10% FBS and Penn / Strep, T-24 cell lines were maintained in McCoy’s 5A medium with 10% FBS and Penn / Strep and primary bladder epithelial (A / T / N): normal human (BdEC) cells were maintained in bladder epithelial cell basal medium (ATCC) supplemented with bladder epithelial g c i g b D W C [ a p 1 fl d t ( m a p c w m ( b l o β S 0 p B S C C e d s i S B m B s a ( S B a p a m t w s i i H 7 w f v D ow nloaded from https://academ ic.oup.com /nar/advance-article/doi/10.1093/nar/gkae1272/7933602 by guest on 30 D ecem ber 2024 rowth factors.

    Article Title: Modulation of ribosomal subunit associations by eIF6 is critical for mitotic exit and cancer progression
    Article Snippet: The human bladder cancer cell lines HT-1376, HT1197, UM-UC-3 and TCCSUP were maintained in EMEM media with 10% FBS and Penn/Strep, T-24 cell lines were maintained in McCoy’s 5A medium with 10% FBS and Penn/Strep, primary bladder epithelial (A/T/N): normal human (BdEC) cells were maintained in bladder epithelial cell basal medium (ATCC) supplemented with bladder epithelial growth factors.

    Article Title: Sequestration of ribosomal subunits as inactive 80S by targeting eIF6 limits mitotic exit and cancer progression
    Article Snippet: The human bladder cancer cell lines HT-1376, HT1197, UM-UC-3 and TCCSUP were maintained in EMEM media with 10% FBS and Penn/Strep, T-24 cell lines were maintained in McCoy’s 5A medium with 10% FBS and Penn/Strep and primary bladder epithelial (A/T/N): normal human (BdEC) cells were maintained in bladder epithelial cell basal medium (ATCC) supplemented with bladder epithelial growth factors.



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    normal human bdec cells  (ATCC)
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    bdec human primary bladder epithelial cells  (ATCC)
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    bdec  (ATCC)
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    ATCC bdec
    A Relative expression of TTK in normal bladder tissues and tumor tissues in the TCGA BLCA and GSE13507 datasets. B Kaplan–Meier survival curves showing the overall survival of patients with low and high TTK expression from the TCGA BLCA and GSE13507 datasets. C Western blot analysis of TTK expression in BC tissues and adjacent normal tissues (n = 24). Densitometric and statistical analysis. D Immunohistochemical staining showing TTK expression levels in BC tissues and corresponding adjacent tissues (original magnification, ×400), quantitatively rated using histochemical scoring (n = 20). (E and F) TTK mRNA and protein expression levels in BC cell lines (TCCSUP, T24, 5637, RT-112, UM-UC-3, and J82) and the primary <t>bladder</t> <t>epithelial</t> cell line <t>BdEC</t> as detected by qRT-PCR ( E ) and Western blot ( F ). Data are expressed as mean ± SD from three independent experiments. * P < 0.05; ** P < 0.01; *** P < 0.001.
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    bdecs  (ATCC)
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    ATCC bdecs
    Evaluation of the antibacterial properties and cytocompatibility of the nanoengineered urinary catheters. a) Optical images of colonies on agar plates and the average colony counts for E. coli and S. aureus . The antibacterial effect of Zn/AgNP‐coated catheters is significantly enhanced (one‐way ANOVA test; n = 6 per group; error bars showed standard deviations; * p < 0.05, ** p < 0.01, and **** p < 0.001). b) Fluorescently stained cellular morphologies and cell viability of human dermal <t>fibroblasts</t> <t>(HDFs)</t> and bladder epithelial cells <t>(BdECs)</t> after 1 d of culturing in extracts (one‐way ANOVA test; n = 6 per group; error bars showed standard deviations; **** p < 0.001).
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    A Relative expression of TTK in normal bladder tissues and tumor tissues in the TCGA BLCA and GSE13507 datasets. B Kaplan–Meier survival curves showing the overall survival of patients with low and high TTK expression from the TCGA BLCA and GSE13507 datasets. C Western blot analysis of TTK expression in BC tissues and adjacent normal tissues (n = 24). Densitometric and statistical analysis. D Immunohistochemical staining showing TTK expression levels in BC tissues and corresponding adjacent tissues (original magnification, ×400), quantitatively rated using histochemical scoring (n = 20). (E and F) TTK mRNA and protein expression levels in BC cell lines (TCCSUP, T24, 5637, RT-112, UM-UC-3, and J82) and the primary bladder epithelial cell line BdEC as detected by qRT-PCR ( E ) and Western blot ( F ). Data are expressed as mean ± SD from three independent experiments. * P < 0.05; ** P < 0.01; *** P < 0.001.

    Journal: Cell Death and Differentiation

    Article Title: TTK promotes mitophagy by regulating ULK1 phosphorylation and pre-mRNA splicing to inhibit mitochondrial apoptosis in bladder cancer

    doi: 10.1038/s41418-025-01492-w

    Figure Lengend Snippet: A Relative expression of TTK in normal bladder tissues and tumor tissues in the TCGA BLCA and GSE13507 datasets. B Kaplan–Meier survival curves showing the overall survival of patients with low and high TTK expression from the TCGA BLCA and GSE13507 datasets. C Western blot analysis of TTK expression in BC tissues and adjacent normal tissues (n = 24). Densitometric and statistical analysis. D Immunohistochemical staining showing TTK expression levels in BC tissues and corresponding adjacent tissues (original magnification, ×400), quantitatively rated using histochemical scoring (n = 20). (E and F) TTK mRNA and protein expression levels in BC cell lines (TCCSUP, T24, 5637, RT-112, UM-UC-3, and J82) and the primary bladder epithelial cell line BdEC as detected by qRT-PCR ( E ) and Western blot ( F ). Data are expressed as mean ± SD from three independent experiments. * P < 0.05; ** P < 0.01; *** P < 0.001.

    Article Snippet: The primary normal bladder epithelial cell line, BdEC (#PCS-420-010, ATCC, USA), was cultured in bladder epithelial cell basal medium supplemented with bladder epithelial growth factors.

    Techniques: Expressing, Western Blot, Immunohistochemical staining, Staining, Quantitative RT-PCR

    Evaluation of the antibacterial properties and cytocompatibility of the nanoengineered urinary catheters. a) Optical images of colonies on agar plates and the average colony counts for E. coli and S. aureus . The antibacterial effect of Zn/AgNP‐coated catheters is significantly enhanced (one‐way ANOVA test; n = 6 per group; error bars showed standard deviations; * p < 0.05, ** p < 0.01, and **** p < 0.001). b) Fluorescently stained cellular morphologies and cell viability of human dermal fibroblasts (HDFs) and bladder epithelial cells (BdECs) after 1 d of culturing in extracts (one‐way ANOVA test; n = 6 per group; error bars showed standard deviations; **** p < 0.001).

    Journal: Advanced Healthcare Materials

    Article Title: Dual‐Layer Nanoengineered Urinary Catheters for Enhanced Antimicrobial Efficacy and Reduced Cytotoxicity

    doi: 10.1002/adhm.202401700

    Figure Lengend Snippet: Evaluation of the antibacterial properties and cytocompatibility of the nanoengineered urinary catheters. a) Optical images of colonies on agar plates and the average colony counts for E. coli and S. aureus . The antibacterial effect of Zn/AgNP‐coated catheters is significantly enhanced (one‐way ANOVA test; n = 6 per group; error bars showed standard deviations; * p < 0.05, ** p < 0.01, and **** p < 0.001). b) Fluorescently stained cellular morphologies and cell viability of human dermal fibroblasts (HDFs) and bladder epithelial cells (BdECs) after 1 d of culturing in extracts (one‐way ANOVA test; n = 6 per group; error bars showed standard deviations; **** p < 0.001).

    Article Snippet: HDFs (PCS‐201‐012, ATCC, USA) and BdECs (PCS‐420‐010, ATCC, USA) were utilized to assess the cytotoxicity of the samples.

    Techniques: Staining