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human ovarian surface epithelial (hose) normal cells  (ScienCell)

 
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    ScienCell human ovarian surface epithelial (hose) normal cells
    Human Ovarian Surface Epithelial (Hose) Normal Cells, supplied by ScienCell, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/normal+human+ovarian+surface+epithelial+%28hose%29+cells/pmc07838621-33-0-10?v=ScienCell
    Average 90 stars, based on 1 article reviews
    human ovarian surface epithelial (hose) normal cells - by Bioz Stars, 2026-08
    90/100 stars

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    Circ_0013958 was upregulated, while miR-637 was downregulated in OC tissues and cells. (A) QRT-PCR assay for the expression of circ_0013958 in OC tissues and adjacent <t>normal</t> tissues ( n = 30). (B) QRT-PCR analysis for the expression of circ_0013958 in OC <t>cell</t> <t>line</t> (SKOV3 and CAOV3) and <t>human</t> <t>ovarian</t> <t>surface</t> <t>epithelial</t> cells (HOSE). (C) ROC curve analysis of the prognostic sensitivity and specificity of circ_0013958 in OC patients in accordance with the 5-year survival of OC patients. (D) QRT-PCR assay for the expression of miR-637 in OC tissues and matched normal tissues ( n = 30). (E) QRT-PCR assay for the expression of miR-637 in HOSE, SKOV3, and CAOV3 cells. (F) Pearson's correlation analysis for the correlation between the expression levels of circ_0013958 and miR-637 in OC tissues ( n = 30). * P < 0.05; ** P < 0.01.
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    Circ_0013958 was upregulated, while miR-637 was downregulated in OC tissues and cells. (A) QRT-PCR assay for the expression of circ_0013958 in OC tissues and adjacent <t>normal</t> tissues ( n = 30). (B) QRT-PCR analysis for the expression of circ_0013958 in OC <t>cell</t> <t>line</t> (SKOV3 and CAOV3) and <t>human</t> <t>ovarian</t> <t>surface</t> <t>epithelial</t> cells (HOSE). (C) ROC curve analysis of the prognostic sensitivity and specificity of circ_0013958 in OC patients in accordance with the 5-year survival of OC patients. (D) QRT-PCR assay for the expression of miR-637 in OC tissues and matched normal tissues ( n = 30). (E) QRT-PCR assay for the expression of miR-637 in HOSE, SKOV3, and CAOV3 cells. (F) Pearson's correlation analysis for the correlation between the expression levels of circ_0013958 and miR-637 in OC tissues ( n = 30). * P < 0.05; ** P < 0.01.
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    Circ_0013958 was upregulated, while miR-637 was downregulated in OC tissues and cells. (A) QRT-PCR assay for the expression of circ_0013958 in OC tissues and adjacent <t>normal</t> tissues ( n = 30). (B) QRT-PCR analysis for the expression of circ_0013958 in OC <t>cell</t> <t>line</t> (SKOV3 and CAOV3) and <t>human</t> <t>ovarian</t> <t>surface</t> <t>epithelial</t> cells (HOSE). (C) ROC curve analysis of the prognostic sensitivity and specificity of circ_0013958 in OC patients in accordance with the 5-year survival of OC patients. (D) QRT-PCR assay for the expression of miR-637 in OC tissues and matched normal tissues ( n = 30). (E) QRT-PCR assay for the expression of miR-637 in HOSE, SKOV3, and CAOV3 cells. (F) Pearson's correlation analysis for the correlation between the expression levels of circ_0013958 and miR-637 in OC tissues ( n = 30). * P < 0.05; ** P < 0.01.
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    normal human ovarian surface epithelial (hose) cells  (ScienCell)
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    Knockdown of HOXA11 antisense ( HOXA11as ) inhibits serous ovarian cancer cell proliferation. (A) Expression of HOXA11as in human ovarian surface <t>epithelial</t> cell line <t>(HOSE)</t> and six ovarian cancer cell lines determined by quantitative real time polymerase chain reaction (qRT-PCR). (B) Knockdown efficiency was determined by qRT-PCR analysis in OVCA429 and SKOV3 cells. Cells were transfected with HOXA11as -specific siRNA (siHOXA11as) and negative control siRNA (siNC). (C, D) Knockdown of HOXA11as significantly reduced cell proliferation in OVCA429 and SKOV3 cells as determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Bars indicate mean±standard deviation of three independent experiments performed in triplicate. * p < 0.05 vs. siNC. siHOXA11as, HOXA11as -specific siRNA.
    Normal Human Ovarian Surface Epithelial (Hose) Cells, supplied by ScienCell, 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


    Circ_0013958 was upregulated, while miR-637 was downregulated in OC tissues and cells. (A) QRT-PCR assay for the expression of circ_0013958 in OC tissues and adjacent normal tissues ( n = 30). (B) QRT-PCR analysis for the expression of circ_0013958 in OC cell line (SKOV3 and CAOV3) and human ovarian surface epithelial cells (HOSE). (C) ROC curve analysis of the prognostic sensitivity and specificity of circ_0013958 in OC patients in accordance with the 5-year survival of OC patients. (D) QRT-PCR assay for the expression of miR-637 in OC tissues and matched normal tissues ( n = 30). (E) QRT-PCR assay for the expression of miR-637 in HOSE, SKOV3, and CAOV3 cells. (F) Pearson's correlation analysis for the correlation between the expression levels of circ_0013958 and miR-637 in OC tissues ( n = 30). * P < 0.05; ** P < 0.01.

    Journal: Frontiers in Genetics

    Article Title: Circular RNA Circ_0013958 Functions as a Tumor Promoter in Ovarian Cancer by Regulating miR-637/PLXNB2 Axis

    doi: 10.3389/fgene.2021.644451

    Figure Lengend Snippet: Circ_0013958 was upregulated, while miR-637 was downregulated in OC tissues and cells. (A) QRT-PCR assay for the expression of circ_0013958 in OC tissues and adjacent normal tissues ( n = 30). (B) QRT-PCR analysis for the expression of circ_0013958 in OC cell line (SKOV3 and CAOV3) and human ovarian surface epithelial cells (HOSE). (C) ROC curve analysis of the prognostic sensitivity and specificity of circ_0013958 in OC patients in accordance with the 5-year survival of OC patients. (D) QRT-PCR assay for the expression of miR-637 in OC tissues and matched normal tissues ( n = 30). (E) QRT-PCR assay for the expression of miR-637 in HOSE, SKOV3, and CAOV3 cells. (F) Pearson's correlation analysis for the correlation between the expression levels of circ_0013958 and miR-637 in OC tissues ( n = 30). * P < 0.05; ** P < 0.01.

    Article Snippet: Normal human ovarian surface epithelial cell line (HOSE; #7310, ScienCell Research Laboratories, Carlsbad, CA, USA) and OC cell lines SKOV3 (ATCC® HTB-77, American Type Culture Collection, Manassas, VA, USA) and CAOV3 (ATCC® HTB-75) were maintained in a Roswell Park Memorial Institute (RPMI)-1640 medium (Gibco, Grand Island, NY, USA), added with 10% fetal bovine serum (FBS; HyClone, Logan, UT, USA) and 1% penicillin/streptomycin (Sigma-Aldrich, St. Louis, MO, USA) at 37°C in the presence of 5% CO 2 .

    Techniques: Quantitative RT-PCR, Expressing

    Knockdown of HOXA11 antisense ( HOXA11as ) inhibits serous ovarian cancer cell proliferation. (A) Expression of HOXA11as in human ovarian surface epithelial cell line (HOSE) and six ovarian cancer cell lines determined by quantitative real time polymerase chain reaction (qRT-PCR). (B) Knockdown efficiency was determined by qRT-PCR analysis in OVCA429 and SKOV3 cells. Cells were transfected with HOXA11as -specific siRNA (siHOXA11as) and negative control siRNA (siNC). (C, D) Knockdown of HOXA11as significantly reduced cell proliferation in OVCA429 and SKOV3 cells as determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Bars indicate mean±standard deviation of three independent experiments performed in triplicate. * p < 0.05 vs. siNC. siHOXA11as, HOXA11as -specific siRNA.

    Journal: Cancer Research and Treatment : Official Journal of Korean Cancer Association

    Article Title: Long Non-coding RNA HOXA11 Antisense Promotes Cell Proliferation and Invasion and Predicts Patient Prognosis in Serous Ovarian Cancer

    doi: 10.4143/crt.2016.263

    Figure Lengend Snippet: Knockdown of HOXA11 antisense ( HOXA11as ) inhibits serous ovarian cancer cell proliferation. (A) Expression of HOXA11as in human ovarian surface epithelial cell line (HOSE) and six ovarian cancer cell lines determined by quantitative real time polymerase chain reaction (qRT-PCR). (B) Knockdown efficiency was determined by qRT-PCR analysis in OVCA429 and SKOV3 cells. Cells were transfected with HOXA11as -specific siRNA (siHOXA11as) and negative control siRNA (siNC). (C, D) Knockdown of HOXA11as significantly reduced cell proliferation in OVCA429 and SKOV3 cells as determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Bars indicate mean±standard deviation of three independent experiments performed in triplicate. * p < 0.05 vs. siNC. siHOXA11as, HOXA11as -specific siRNA.

    Article Snippet: Normal human ovarian surface epithelial (HOSE) cells were purchased from ScienCell Research Laboratories (San Diego, CA).

    Techniques: Knockdown, Expressing, Real-time Polymerase Chain Reaction, Quantitative RT-PCR, Transfection, Negative Control, MTT Assay, Standard Deviation