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skov3 human epithelial ovary cancer cell line  (ATCC)


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    Structured Review

    ATCC skov3 human epithelial ovary cancer cell line
    Attachment assay of <t>SKOV3</t> cells treated with 10 and 20 μM curcumin for 6 h. Once the curcumin was washed out, the attachment assays were performed after 6, 24, and 48 h
    Skov3 Human Epithelial Ovary Cancer Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 8000 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/skov3 human epithelial ovary cancer cell line/product/ATCC
    Average 99 stars, based on 8000 article reviews
    skov3 human epithelial ovary cancer cell line - by Bioz Stars, 2026-02
    99/100 stars

    Images

    1) Product Images from "The inhibitory effect of curcumin via fascin suppression through JAK/STAT3 pathway on metastasis and recurrence of ovary cancer cells"

    Article Title: The inhibitory effect of curcumin via fascin suppression through JAK/STAT3 pathway on metastasis and recurrence of ovary cancer cells

    Journal: BMC Women's Health

    doi: 10.1186/s12905-020-01122-2

    Attachment assay of SKOV3 cells treated with 10 and 20 μM curcumin for 6 h. Once the curcumin was washed out, the attachment assays were performed after 6, 24, and 48 h
    Figure Legend Snippet: Attachment assay of SKOV3 cells treated with 10 and 20 μM curcumin for 6 h. Once the curcumin was washed out, the attachment assays were performed after 6, 24, and 48 h

    Techniques Used:



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    ATCC skov3 human epithelial ovary cancer cell line
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    ATCC human ovary cancer cell lines skov3
    Attachment assay of <t>SKOV3</t> cells treated with 10 and 20 μM curcumin for 6 h. Once the curcumin was washed out, the attachment assays were performed after 6, 24, and 48 h
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    ATCC human ovary cancer cell line skov3
    Mutant p53 proteins lose the interaction with the microprocessing Drosha complex. (a) Co-IP experiments demonstrated a loss of interaction with the Drosha complex in cell models expressing various mutated forms of p53. <t>SKOV3</t> cell lines (p53 null) stably expressed p53 mutant proteins (6 oncomorphic mutations (R175H, R248Q, R248Q.P72R, R273C, R273L, and R273S) and 1 unclassified mutation (I195T). IP of DDX5 or p53 detected binding of p53 in the WT UCI-107 cell lines, but not in any other cell lines with mutant p53 proteins. (b) WT p53-responsive miRNA expression in SKOV3 cells expressing R248Q.P72R p53 mutant at a time course after radiation treatment.
    Human Ovary Cancer Cell Line Skov3, 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
    https://www.bioz.com/result/human ovary cancer cell line skov3/product/ATCC
    Average 99 stars, based on 1 article reviews
    human ovary cancer cell line skov3 - by Bioz Stars, 2026-02
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      Buy from Supplier

    Image Search Results


    Attachment assay of SKOV3 cells treated with 10 and 20 μM curcumin for 6 h. Once the curcumin was washed out, the attachment assays were performed after 6, 24, and 48 h

    Journal: BMC Women's Health

    Article Title: The inhibitory effect of curcumin via fascin suppression through JAK/STAT3 pathway on metastasis and recurrence of ovary cancer cells

    doi: 10.1186/s12905-020-01122-2

    Figure Lengend Snippet: Attachment assay of SKOV3 cells treated with 10 and 20 μM curcumin for 6 h. Once the curcumin was washed out, the attachment assays were performed after 6, 24, and 48 h

    Article Snippet: Cell lines were derived from the SKOV3 human epithelial ovary cancer cell line (ATCC, Manassas, VA, United States) [ ].

    Techniques:

    Mutant p53 proteins lose the interaction with the microprocessing Drosha complex. (a) Co-IP experiments demonstrated a loss of interaction with the Drosha complex in cell models expressing various mutated forms of p53. SKOV3 cell lines (p53 null) stably expressed p53 mutant proteins (6 oncomorphic mutations (R175H, R248Q, R248Q.P72R, R273C, R273L, and R273S) and 1 unclassified mutation (I195T). IP of DDX5 or p53 detected binding of p53 in the WT UCI-107 cell lines, but not in any other cell lines with mutant p53 proteins. (b) WT p53-responsive miRNA expression in SKOV3 cells expressing R248Q.P72R p53 mutant at a time course after radiation treatment.

    Journal: Journal of cancer therapy

    Article Title: Oncomorphic TP 53 Mutations in Gynecologic Cancers Lose the Normal Protein:Protein Interactions with the microRNA Microprocessing Complex

    doi: 10.4236/jct.2014.56058

    Figure Lengend Snippet: Mutant p53 proteins lose the interaction with the microprocessing Drosha complex. (a) Co-IP experiments demonstrated a loss of interaction with the Drosha complex in cell models expressing various mutated forms of p53. SKOV3 cell lines (p53 null) stably expressed p53 mutant proteins (6 oncomorphic mutations (R175H, R248Q, R248Q.P72R, R273C, R273L, and R273S) and 1 unclassified mutation (I195T). IP of DDX5 or p53 detected binding of p53 in the WT UCI-107 cell lines, but not in any other cell lines with mutant p53 proteins. (b) WT p53-responsive miRNA expression in SKOV3 cells expressing R248Q.P72R p53 mutant at a time course after radiation treatment.

    Article Snippet: The human ovary cancer cell line SKOV3 was purchased from American Tissue Culture Collection (ATCC, Bethesda, MD).

    Techniques: Mutagenesis, Co-Immunoprecipitation Assay, Expressing, Stable Transfection, Binding Assay