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3a8  (ATCC)


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    Structured Review

    ATCC 3a8
    3a8, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/3a8/product/ATCC
    Average 94 stars, based on 12 article reviews
    3a8 - by Bioz Stars, 2026-03
    94/100 stars

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    Thermo Fisher anti-foxa1 (3a8 pima1091
    Expression levels of NKX3.1 vary across PCa cell lines and closely track with AR expression levels. ( A ) Western blot illustrating AR, NKX3.1, and B-actin protein levels in benign prostate cell lines and adenocarcinoma prostate cell lines. ( B ) Western blot illustrating protein levels of AR and NKX3.1 in AR-null cell lines and AR-positive cell lines. ( C ) Co-immunoprecipitation Western blot of LNCaP cells with IgG, AR, <t>FOXA1,</t> and NKX3.1 pulldown. ( D ) Co-immunoprecipitation Western blot of CWR-R1 cells with IgG, AR, FOXA1, and NKX3.1 pulldown. ( E ) Nano-BiT luminescence data depicting binding of large BiT (Lg) and small (Sm) BiT partners on constructs tagged on N- or C-terminally expressed AR, NKX3.1, and/or FOXA1. Significance was determined via one-way ANOVA comparing signal to each individual single BiT. The threshold for statistical significance set as follows: non-significant (ns) p > 0.05, * p < 0.05, *** p < 0.001, **** p < 0.0001.
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    Expression levels of NKX3.1 vary across PCa cell lines and closely track with AR expression levels. ( A ) Western blot illustrating AR, NKX3.1, and B-actin protein levels in benign prostate cell lines and adenocarcinoma prostate cell lines. ( B ) Western blot illustrating protein levels of AR and NKX3.1 in AR-null cell lines and AR-positive cell lines. ( C ) Co-immunoprecipitation Western blot of LNCaP cells with IgG, AR, FOXA1, and NKX3.1 pulldown. ( D ) Co-immunoprecipitation Western blot of CWR-R1 cells with IgG, AR, FOXA1, and NKX3.1 pulldown. ( E ) Nano-BiT luminescence data depicting binding of large BiT (Lg) and small (Sm) BiT partners on constructs tagged on N- or C-terminally expressed AR, NKX3.1, and/or FOXA1. Significance was determined via one-way ANOVA comparing signal to each individual single BiT. The threshold for statistical significance set as follows: non-significant (ns) p > 0.05, * p < 0.05, *** p < 0.001, **** p < 0.0001.

    Journal: Cancers

    Article Title: The Homeobox Transcription Factor NKX3.1 Displays an Oncogenic Role in Castration-Resistant Prostate Cancer Cells

    doi: 10.3390/cancers17020306

    Figure Lengend Snippet: Expression levels of NKX3.1 vary across PCa cell lines and closely track with AR expression levels. ( A ) Western blot illustrating AR, NKX3.1, and B-actin protein levels in benign prostate cell lines and adenocarcinoma prostate cell lines. ( B ) Western blot illustrating protein levels of AR and NKX3.1 in AR-null cell lines and AR-positive cell lines. ( C ) Co-immunoprecipitation Western blot of LNCaP cells with IgG, AR, FOXA1, and NKX3.1 pulldown. ( D ) Co-immunoprecipitation Western blot of CWR-R1 cells with IgG, AR, FOXA1, and NKX3.1 pulldown. ( E ) Nano-BiT luminescence data depicting binding of large BiT (Lg) and small (Sm) BiT partners on constructs tagged on N- or C-terminally expressed AR, NKX3.1, and/or FOXA1. Significance was determined via one-way ANOVA comparing signal to each individual single BiT. The threshold for statistical significance set as follows: non-significant (ns) p > 0.05, * p < 0.05, *** p < 0.001, **** p < 0.0001.

    Article Snippet: Antibodies used: anti-AR (D6F11 XP ® , Cell Signaling Technology, (Danvers, MA, USA)); anti-Beta Actin (AC-15, Sigma-Aldrich); anti-FOXA1 (3A8 PIMA1091, Thermo Fisher); anti-NKX3.1 [D2Y1A XP ® , Cell Signaling Technology, (Danvers, MA, USA)]; anti-Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) (Cell Signaling, Cat. #2118); and anti-cleaved PARP [Asp214 D64E10 XP ® , Cell Signaling Technology, (Danvers, MA, USA)].

    Techniques: Expressing, Western Blot, Immunoprecipitation, Binding Assay, Construct