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normal human intestinal epithelial cell line hiec  (ATCC)


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    ATCC normal human intestinal epithelial cell line hiec
    Normal Human Intestinal Epithelial Cell Line Hiec, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 234 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/normal+human+intestinal+epithelial+cell+line+hiec/HIEC-6/pmc12862372-50-13-23
    Average 96 stars, based on 234 article reviews
    normal human intestinal epithelial cell line hiec - by Bioz Stars, 2026-09
    96/100 stars

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    Article Title: GRIM-19 repressed hypoxia-induced invasion and EMT of colorectal cancer by repressing autophagy through inactivation of STAT3/HIF-1α signaling axis.
    Article Snippet: Correspondence Kiyohito Tanaka, Department of Gastroenterology, Kyoto Second Red Cross Hospital, Kyoto, 602‐8026 Japan.. Email: seijin7705@gmail.com Shuixiang He, Department of Gastroenterology, The First Affiliated Hospital of Xi’an Jiaotong University, Yan Tower West Road No. 277, Xi’an, 710061 Shaanxi, People’s Republic of China.. Email: dyyyjxk@mail.xjtu.edu.cn Abstract Hypoxia leads to cancer progression and promotes the metastatic potential of cancer cells.

    Article Title: The fluoropyrimidine polymer CF10 synergizes with 5-ethynyl-2′-deoxyuridine by promoting telomere attrition and mitotic catastrophe
    Article Snippet: Human colorectal carcinoma cell line HCT116, human colonic adenocarcinoma cell line LS174T, and normal human intestinal epithelial cell line HIEC-6 were obtained from ATCC (ATCC numbers: CCL-247, CL-188, and CRL-3266, respectively).



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    LncRNA HANR facilitates CHOL cell proliferation and migration in vitro A. RT-qPCR analysis measured HANR expression in CHOL cells (TFK-1, RBE and SSP-25, HuCC-T1) and normal human <t>intestinal</t> <t>epithelial</t> cells <t>HIEC.</t> Functional assays were done with CHOL cells with transfection of sh-NC, sh-HANR#1 or sh-HANR#2. B. CCK-8 assay evaluated the viability of CHOL cells at 24h, 48h and 72h. C. The proliferation of transfected CHOL cells was measured via 14-day colony formation assay. D. The migration of transfected CHOL cells was testified by measurement of wound width in wound healing assay (magnification × 100). E. CHOL cell migration was assessed by transwell assay after HANR was stably knocked down (magnification × 100). Data acquired from three independent experiments were exhibited as the mean ± SD. *P < 0.05, **P < 0.01.
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    LncRNA HANR facilitates CHOL cell proliferation and migration in vitro A. RT-qPCR analysis measured HANR expression in CHOL cells (TFK-1, RBE and SSP-25, HuCC-T1) and normal human intestinal epithelial cells HIEC. Functional assays were done with CHOL cells with transfection of sh-NC, sh-HANR#1 or sh-HANR#2. B. CCK-8 assay evaluated the viability of CHOL cells at 24h, 48h and 72h. C. The proliferation of transfected CHOL cells was measured via 14-day colony formation assay. D. The migration of transfected CHOL cells was testified by measurement of wound width in wound healing assay (magnification × 100). E. CHOL cell migration was assessed by transwell assay after HANR was stably knocked down (magnification × 100). Data acquired from three independent experiments were exhibited as the mean ± SD. *P < 0.05, **P < 0.01.

    Journal: Heliyon

    Article Title: LncRNA-HANR exacerbates malignant behaviors of cholangiocarcinoma cells through activating Notch pathway

    doi: 10.1016/j.heliyon.2023.e22087

    Figure Lengend Snippet: LncRNA HANR facilitates CHOL cell proliferation and migration in vitro A. RT-qPCR analysis measured HANR expression in CHOL cells (TFK-1, RBE and SSP-25, HuCC-T1) and normal human intestinal epithelial cells HIEC. Functional assays were done with CHOL cells with transfection of sh-NC, sh-HANR#1 or sh-HANR#2. B. CCK-8 assay evaluated the viability of CHOL cells at 24h, 48h and 72h. C. The proliferation of transfected CHOL cells was measured via 14-day colony formation assay. D. The migration of transfected CHOL cells was testified by measurement of wound width in wound healing assay (magnification × 100). E. CHOL cell migration was assessed by transwell assay after HANR was stably knocked down (magnification × 100). Data acquired from three independent experiments were exhibited as the mean ± SD. *P < 0.05, **P < 0.01.

    Article Snippet: The above-mentioned cells and human normal intestinal epithelial cell line HIEC (ATCC, Manassas, VA, USA) were incubated in an environment with 5 % CO 2 at 37 °C.

    Techniques: Migration, In Vitro, Quantitative RT-PCR, Expressing, Functional Assay, Transfection, CCK-8 Assay, Colony Assay, Wound Healing Assay, Transwell Assay, Stable Transfection