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brca2  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc brca2
    Brca2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 80 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/brca2/product/Cell Signaling Technology Inc
    Average 95 stars, based on 80 article reviews
    brca2 - by Bioz Stars, 2026-04
    95/100 stars

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    Cell Signaling Technology Inc rabbit anti brca2
    BRCA1/2 Mutations and Deep Deletions Link to Poor Outcomes. (A-B) Frequency of BRCA1 (A) and <t>BRCA2</t> (B) Alterations, Including Mutations (red) and Deep Deletions (Blue), Across the cBioPortal for Cancer Genomics Database for Prostate Cancer. The Patient-Weighted Average Alteration Frequency is Indicated by a Dashed Vertical Line. (C) Kaplan–Meier Analysis of Overall Survival Comparing Patients with BRCA1/2 Alterations (Red) to Those Without (Blue), Demonstrating Significantly Reduced Survival in the Altered Group. Δ Median Survival = 27.89 Months. n = 308 in BRCA1/2 Altered Group; n = 3717 in the Unaltered Group. (D) Schematic of CRISPR-Cas9-Mediated Knockout (KO) of BRCA1 or BRCA2 in Prostate Cancer Cell Lines LNCaP. (E) Representative Virtual Lanes of Simple Western Validation of BRCA1 and BRCA2 Knockout Efficiency. (F) Representative Lane View and Densitometric Quantification Normalized to Vinculin are Shown. Graphs Represent Mean ± SEM from Three-Four Independent Experiments.
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    BRCA1/2 Mutations and Deep Deletions Link to Poor Outcomes. (A-B) Frequency of BRCA1 (A) and BRCA2 (B) Alterations, Including Mutations (red) and Deep Deletions (Blue), Across the cBioPortal for Cancer Genomics Database for Prostate Cancer. The Patient-Weighted Average Alteration Frequency is Indicated by a Dashed Vertical Line. (C) Kaplan–Meier Analysis of Overall Survival Comparing Patients with BRCA1/2 Alterations (Red) to Those Without (Blue), Demonstrating Significantly Reduced Survival in the Altered Group. Δ Median Survival = 27.89 Months. n = 308 in BRCA1/2 Altered Group; n = 3717 in the Unaltered Group. (D) Schematic of CRISPR-Cas9-Mediated Knockout (KO) of BRCA1 or BRCA2 in Prostate Cancer Cell Lines LNCaP. (E) Representative Virtual Lanes of Simple Western Validation of BRCA1 and BRCA2 Knockout Efficiency. (F) Representative Lane View and Densitometric Quantification Normalized to Vinculin are Shown. Graphs Represent Mean ± SEM from Three-Four Independent Experiments.

    Journal: Technology in Cancer Research & Treatment

    Article Title: Combined DNA-PK and PARP Inhibition as a Therapeutic Strategy in BRCA-Mutated Prostate Cancer: An in Vitro Pilot Study

    doi: 10.1177/15330338251394948

    Figure Lengend Snippet: BRCA1/2 Mutations and Deep Deletions Link to Poor Outcomes. (A-B) Frequency of BRCA1 (A) and BRCA2 (B) Alterations, Including Mutations (red) and Deep Deletions (Blue), Across the cBioPortal for Cancer Genomics Database for Prostate Cancer. The Patient-Weighted Average Alteration Frequency is Indicated by a Dashed Vertical Line. (C) Kaplan–Meier Analysis of Overall Survival Comparing Patients with BRCA1/2 Alterations (Red) to Those Without (Blue), Demonstrating Significantly Reduced Survival in the Altered Group. Δ Median Survival = 27.89 Months. n = 308 in BRCA1/2 Altered Group; n = 3717 in the Unaltered Group. (D) Schematic of CRISPR-Cas9-Mediated Knockout (KO) of BRCA1 or BRCA2 in Prostate Cancer Cell Lines LNCaP. (E) Representative Virtual Lanes of Simple Western Validation of BRCA1 and BRCA2 Knockout Efficiency. (F) Representative Lane View and Densitometric Quantification Normalized to Vinculin are Shown. Graphs Represent Mean ± SEM from Three-Four Independent Experiments.

    Article Snippet: Primary antibodies were used at a 1:100 dilution and included mouse anti-Vinculin (MAB6896, Bio-Techne, Minneapolis, MN, USA), rabbit anti- BRCA2 (10741S, Cell Signaling Technology, Danvers, MA, USA), mouse anti-BRCA1 (NB100-598, Bio-Techne, Minneapolis, MN, USA), and rabbit anti- DNA PKcs (ab32566, Abcam, Cambridge, UK).

    Techniques: CRISPR, Knock-Out, Simple Western, Biomarker Discovery

    Schematic Representation of the Study's Objective, Focusing on the Therapeutic Potential of DNA-PK Inhibitors Combined with PARP Inhibitors in Prostate Cancer with BRCA1 and BRCA2 Gene Mutations. Created in BioRender (Mazumdar).

    Journal: Technology in Cancer Research & Treatment

    Article Title: Combined DNA-PK and PARP Inhibition as a Therapeutic Strategy in BRCA-Mutated Prostate Cancer: An in Vitro Pilot Study

    doi: 10.1177/15330338251394948

    Figure Lengend Snippet: Schematic Representation of the Study's Objective, Focusing on the Therapeutic Potential of DNA-PK Inhibitors Combined with PARP Inhibitors in Prostate Cancer with BRCA1 and BRCA2 Gene Mutations. Created in BioRender (Mazumdar).

    Article Snippet: Primary antibodies were used at a 1:100 dilution and included mouse anti-Vinculin (MAB6896, Bio-Techne, Minneapolis, MN, USA), rabbit anti- BRCA2 (10741S, Cell Signaling Technology, Danvers, MA, USA), mouse anti-BRCA1 (NB100-598, Bio-Techne, Minneapolis, MN, USA), and rabbit anti- DNA PKcs (ab32566, Abcam, Cambridge, UK).

    Techniques: