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brca2  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology brca2
    Brca2, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/brca2/BRCA2+siRNA/pm20127002-36-0-5
    Average 90 stars, based on 14 article reviews
    brca2 - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Transfection:

    Article Title: Complementary genetic screens identify the E3 ubiquitin ligase CBLC, as a modifier of PARP inhibitor sensitivity.
    Article Snippet: .. Each experiment was repeated twice. cell-based assays Cell lines were transfected with SMARTpool siRNAs (Dharmacon, GE Healthcare) targeting BRCA2 and CBLC or siCONTROL A (Santa Cruz Biotech) using RNAiMax (Invitrogen) transfection reagent. ..

    Article Title: Inhibition of c‐MET increases the antitumour activity of PARP inhibitors in gastric cancer models
    Article Snippet: .. For the siRNA transfection experiments, we use siRNA for stable knockdown of c‐MET (sc‐35924), BRCA1 (sc‐29219) and BRCA2 (sc‐29825) and control (sc‐37007) from Santa Cruz Biotechnology and Lipofectamine 3000 (#L3000‐15 Invitrogen Corp.). ..

    Article Title: Silencing of BRCA2 decreases anoikis and its heterologous expression sensitizes yeast cells to acetic acid-induced programmed cell death.
    Article Snippet: Adhesion of normal epithelial cells to the extracellular matrix (ECM) is essential for survival.. Cell detachment from ECM induces a specific form of programmed cell death (PCD) termed anoikis.. BRCA2, a tumor suppressor gene whose mutations confer predisposition to cancer, has been implicated in the regulation of DNA repair, transcription, cell proliferation, and apoptosis.

    other:

    Article Title: Profilin-1 regulates DNA replication forks in a context-dependent fashion by interacting with SNF2H and BOD1L.
    Article Snippet: Small interfering RNAs targeting human BOD1L/FAM44A (#sc-88933), SMARCAL1 (#sc-63042), BRCA1 (#sc-29219), BRCA2 (#sc-29825), and FBH1/FBXO18 (#sc-90469) were purchased from Santa Cruz Biotechnology, Inc.

    Article Title: Profilin-1 regulates DNA replication forks in a context-dependent fashion by interacting with SNF2H and BOD1L
    Article Snippet: Small interfering RNAs targeting human BOD1L/FAM44A (#sc-88933), SMARCAL1 (#sc-63042), BRCA1 (#sc-29219), BRCA2 (#sc-29825), and FBH1/FBXO18 (#sc-90469) were purchased from Santa Cruz Biotechnology, Inc.

    Control:

    Article Title: Targeting HR Repair as a Synthetic Lethal Approach to Increase DNA Damage Sensitivity by a RAD52 Inhibitor in BRCA2-Deficient Cancer Cells
    Article Snippet: .. For transient depletion of BRCA2 in MCF7 cells, we purchased siRNA against BRCA2 (sc-29825) and control (sc-37007) from Santa Cruz Biotech (CA, USA). ..

    Article Title: Inhibition of c‐MET increases the antitumour activity of PARP inhibitors in gastric cancer models
    Article Snippet: .. For the siRNA transfection experiments, we use siRNA for stable knockdown of c‐MET (sc‐35924), BRCA1 (sc‐29219) and BRCA2 (sc‐29825) and control (sc‐37007) from Santa Cruz Biotechnology and Lipofectamine 3000 (#L3000‐15 Invitrogen Corp.). ..

    Knockdown:

    Article Title: Inhibition of c‐MET increases the antitumour activity of PARP inhibitors in gastric cancer models
    Article Snippet: .. For the siRNA transfection experiments, we use siRNA for stable knockdown of c‐MET (sc‐35924), BRCA1 (sc‐29219) and BRCA2 (sc‐29825) and control (sc‐37007) from Santa Cruz Biotechnology and Lipofectamine 3000 (#L3000‐15 Invitrogen Corp.). ..

    Over Expression:

    Article Title: Interaction of FUS and HDAC1 Regulates DNA Damage Response and Repair in Neurons
    Article Snippet: For LacR constructs, FUS and HDAC1 were cloned into Cherry-LacRep (Addgene plasmid 18985). .. FUS overexpression constructs were generated by fusing mCherry to the N-terminal of FUS and subcloning this into the Lv-CAG lentiviral vector. siRNAs siRNAs against FUS (sc-40563), BRCA2 (sc-29825) and LIG4 (sc-37394) were purchased from Santa Cruz biotech. ..

    Construct:

    Article Title: Interaction of FUS and HDAC1 Regulates DNA Damage Response and Repair in Neurons
    Article Snippet: For LacR constructs, FUS and HDAC1 were cloned into Cherry-LacRep (Addgene plasmid 18985). .. FUS overexpression constructs were generated by fusing mCherry to the N-terminal of FUS and subcloning this into the Lv-CAG lentiviral vector. siRNAs siRNAs against FUS (sc-40563), BRCA2 (sc-29825) and LIG4 (sc-37394) were purchased from Santa Cruz biotech. ..

    Generated:

    Article Title: Interaction of FUS and HDAC1 Regulates DNA Damage Response and Repair in Neurons
    Article Snippet: For LacR constructs, FUS and HDAC1 were cloned into Cherry-LacRep (Addgene plasmid 18985). .. FUS overexpression constructs were generated by fusing mCherry to the N-terminal of FUS and subcloning this into the Lv-CAG lentiviral vector. siRNAs siRNAs against FUS (sc-40563), BRCA2 (sc-29825) and LIG4 (sc-37394) were purchased from Santa Cruz biotech. ..

    Subcloning:

    Article Title: Interaction of FUS and HDAC1 Regulates DNA Damage Response and Repair in Neurons
    Article Snippet: For LacR constructs, FUS and HDAC1 were cloned into Cherry-LacRep (Addgene plasmid 18985). .. FUS overexpression constructs were generated by fusing mCherry to the N-terminal of FUS and subcloning this into the Lv-CAG lentiviral vector. siRNAs siRNAs against FUS (sc-40563), BRCA2 (sc-29825) and LIG4 (sc-37394) were purchased from Santa Cruz biotech. ..

    shRNA:

    Article Title: Silencing of BRCA2 decreases anoikis and its heterologous expression sensitizes yeast cells to acetic acid-induced programmed cell death.
    Article Snippet: Adhesion of normal epithelial cells to the extracellular matrix (ECM) is essential for survival.. Cell detachment from ECM induces a specific form of programmed cell death (PCD) termed anoikis.. BRCA2, a tumor suppressor gene whose mutations confer predisposition to cancer, has been implicated in the regulation of DNA repair, transcription, cell proliferation, and apoptosis.

    Expressing:

    Article Title: Silencing of BRCA2 decreases anoikis and its heterologous expression sensitizes yeast cells to acetic acid-induced programmed cell death.
    Article Snippet: Adhesion of normal epithelial cells to the extracellular matrix (ECM) is essential for survival.. Cell detachment from ECM induces a specific form of programmed cell death (PCD) termed anoikis.. BRCA2, a tumor suppressor gene whose mutations confer predisposition to cancer, has been implicated in the regulation of DNA repair, transcription, cell proliferation, and apoptosis.

    Western Blot:

    Article Title: Silencing of BRCA2 decreases anoikis and its heterologous expression sensitizes yeast cells to acetic acid-induced programmed cell death.
    Article Snippet: Adhesion of normal epithelial cells to the extracellular matrix (ECM) is essential for survival.. Cell detachment from ECM induces a specific form of programmed cell death (PCD) termed anoikis.. BRCA2, a tumor suppressor gene whose mutations confer predisposition to cancer, has been implicated in the regulation of DNA repair, transcription, cell proliferation, and apoptosis.



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    (A) . U2OS or Hela cells were transfected with Control (siCON), MCPH1 (siMCPH1) or <t>BRCA2</t> (siBRCA2) siRNA for 48h or 120h and protein expression analysed via Western blotting with the indicated antibodies. MCPH1 expression in sgCON (control) and sgMCPH1 (MCPH1 knockout) cells was also investigated by Western blotting. (B) Quantification of MCPH1 or BRCA2 protein bands normalised to GAPDH and expressed as % change relative to siCON or sgCON. Data is the mean and standard error of three (48h) or two (120h and sgCON/sgMCPH1) independent experiments. (C) U2OS or Hela cells were transfected with MCPH1 siRNA for 72h before analysis of nuclear morphology (premature chromosome condensation, PCC) via DAPI staining and fluorescence microscopy. (D) The % of cells displaying PCC, with at least 100 cells analysed.
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    Image Search Results


    The potential function and pathways of TSF on DOX‐induced cardiotoxicity: (a) PPI network of 103 overlapping targets constructed based on the STRING database; (b) the PPI network map; (c) the molecular docking of HDAC8 with BRCA2.

    Journal: Food Science & Nutrition

    Article Title: Exploring the Mechanisms of Total Saponins of Black Ginseng and Ginsenoside Rg3 Against Doxorubicin‐Induced Cardiotoxicity

    doi: 10.1002/fsn3.71968

    Figure Lengend Snippet: The potential function and pathways of TSF on DOX‐induced cardiotoxicity: (a) PPI network of 103 overlapping targets constructed based on the STRING database; (b) the PPI network map; (c) the molecular docking of HDAC8 with BRCA2.

    Article Snippet: Antibodies for BRCA2, DRP1 and Bcl‐2 were sourced from Wanlei Biotechnology Co. Ltd. (Lot: T11052438, T09113028, T11201556), while β ‐actin and HRP‐labeled secondary antibodies were procured from Affinity Biosciences (Lot: T0022, S0001).

    Techniques: Construct

    TSF and Rg3 regulate HDAC8/BRCA2/DRP1 pathway inhibits DOX‐induced cardiomyocyte apoptosis. (a) Apoptosis was assessed using TUNEL staining (Scale bar = 50 μm). (b) The results of western blotting for each group. (c) The expression of Bcl‐2 for each group. (d) The expression of DRP1 for each group. (e) The expression of HDAC8 for each group. (f) The expression of BRCA2 for each group. (g) Immunofluorescence staining for observing the colocalization of HDAC8, BRCA2, and DRP1 (Scale bar = 1 mm). Data are expressed as mean ± standard from three individual experiments. Data analysis among groups was performed using ANOVA, with LSD for equal variances and Dunnett’s‐T3 for unequal variances, with significance levels of * p < 0.05, ** p < 0.01, *** p < 0.001.

    Journal: Food Science & Nutrition

    Article Title: Exploring the Mechanisms of Total Saponins of Black Ginseng and Ginsenoside Rg3 Against Doxorubicin‐Induced Cardiotoxicity

    doi: 10.1002/fsn3.71968

    Figure Lengend Snippet: TSF and Rg3 regulate HDAC8/BRCA2/DRP1 pathway inhibits DOX‐induced cardiomyocyte apoptosis. (a) Apoptosis was assessed using TUNEL staining (Scale bar = 50 μm). (b) The results of western blotting for each group. (c) The expression of Bcl‐2 for each group. (d) The expression of DRP1 for each group. (e) The expression of HDAC8 for each group. (f) The expression of BRCA2 for each group. (g) Immunofluorescence staining for observing the colocalization of HDAC8, BRCA2, and DRP1 (Scale bar = 1 mm). Data are expressed as mean ± standard from three individual experiments. Data analysis among groups was performed using ANOVA, with LSD for equal variances and Dunnett’s‐T3 for unequal variances, with significance levels of * p < 0.05, ** p < 0.01, *** p < 0.001.

    Article Snippet: Antibodies for BRCA2, DRP1 and Bcl‐2 were sourced from Wanlei Biotechnology Co. Ltd. (Lot: T11052438, T09113028, T11201556), while β ‐actin and HRP‐labeled secondary antibodies were procured from Affinity Biosciences (Lot: T0022, S0001).

    Techniques: TUNEL Assay, Staining, Western Blot, Expressing, Immunofluorescence

    The mechanism diagram of TSF and Rg3 alleviating DOX‐induced myocardial injury by regulating the HDAC8/BRCA2/DRP1 pathway.

    Journal: Food Science & Nutrition

    Article Title: Exploring the Mechanisms of Total Saponins of Black Ginseng and Ginsenoside Rg3 Against Doxorubicin‐Induced Cardiotoxicity

    doi: 10.1002/fsn3.71968

    Figure Lengend Snippet: The mechanism diagram of TSF and Rg3 alleviating DOX‐induced myocardial injury by regulating the HDAC8/BRCA2/DRP1 pathway.

    Article Snippet: Antibodies for BRCA2, DRP1 and Bcl‐2 were sourced from Wanlei Biotechnology Co. Ltd. (Lot: T11052438, T09113028, T11201556), while β ‐actin and HRP‐labeled secondary antibodies were procured from Affinity Biosciences (Lot: T0022, S0001).

    Techniques:

    (A) . U2OS or Hela cells were transfected with Control (siCON), MCPH1 (siMCPH1) or BRCA2 (siBRCA2) siRNA for 48h or 120h and protein expression analysed via Western blotting with the indicated antibodies. MCPH1 expression in sgCON (control) and sgMCPH1 (MCPH1 knockout) cells was also investigated by Western blotting. (B) Quantification of MCPH1 or BRCA2 protein bands normalised to GAPDH and expressed as % change relative to siCON or sgCON. Data is the mean and standard error of three (48h) or two (120h and sgCON/sgMCPH1) independent experiments. (C) U2OS or Hela cells were transfected with MCPH1 siRNA for 72h before analysis of nuclear morphology (premature chromosome condensation, PCC) via DAPI staining and fluorescence microscopy. (D) The % of cells displaying PCC, with at least 100 cells analysed.

    Journal: PLOS One

    Article Title: Differential sensitivity of MCPH1- and BRCA2-deficient cancer cells to PARP-1 inhibition

    doi: 10.1371/journal.pone.0345514

    Figure Lengend Snippet: (A) . U2OS or Hela cells were transfected with Control (siCON), MCPH1 (siMCPH1) or BRCA2 (siBRCA2) siRNA for 48h or 120h and protein expression analysed via Western blotting with the indicated antibodies. MCPH1 expression in sgCON (control) and sgMCPH1 (MCPH1 knockout) cells was also investigated by Western blotting. (B) Quantification of MCPH1 or BRCA2 protein bands normalised to GAPDH and expressed as % change relative to siCON or sgCON. Data is the mean and standard error of three (48h) or two (120h and sgCON/sgMCPH1) independent experiments. (C) U2OS or Hela cells were transfected with MCPH1 siRNA for 72h before analysis of nuclear morphology (premature chromosome condensation, PCC) via DAPI staining and fluorescence microscopy. (D) The % of cells displaying PCC, with at least 100 cells analysed.

    Article Snippet: Membranes were blocked with 5% dried skimmed milk/TBS-T (50mM Tris pH 7.6, 150mM NaCl and 0.2% v/v Tween-20) for a minimum of 1-hour prior to overnight incubation at 4°C with primary antibodies; MCPH1 (11962–1-AP, Proteintech), BRCA2 (29450–1-AP, Proteintech) and GAPDH (60004–1-Ig, Proteintech).

    Techniques: Transfection, Control, Expressing, Western Blot, Knock-Out, Staining, Fluorescence, Microscopy

    U2OS cells were transfected with control (siCON), BRCA2 (siBRCA2) or BRCA2 + MCPH1 (siBRCA2 + siMCPH1) siRNA for 48h before (A) Western blot analysis or (B) seeding into 96-well plates and treating with the indicated doses of AZD2461 or Talazoparib, with each treatment performed in triplicate. After 96-hours, cell viability was measured using an MTS assay. MTS data represents the mean and standard error from at least three independent experiments, with cell viability expressed as a % relative to the corresponding untreated sample. Statistical significance was measured using two-way ANOVA (p-values described in text, with significance set at p < 0.05).

    Journal: PLOS One

    Article Title: Differential sensitivity of MCPH1- and BRCA2-deficient cancer cells to PARP-1 inhibition

    doi: 10.1371/journal.pone.0345514

    Figure Lengend Snippet: U2OS cells were transfected with control (siCON), BRCA2 (siBRCA2) or BRCA2 + MCPH1 (siBRCA2 + siMCPH1) siRNA for 48h before (A) Western blot analysis or (B) seeding into 96-well plates and treating with the indicated doses of AZD2461 or Talazoparib, with each treatment performed in triplicate. After 96-hours, cell viability was measured using an MTS assay. MTS data represents the mean and standard error from at least three independent experiments, with cell viability expressed as a % relative to the corresponding untreated sample. Statistical significance was measured using two-way ANOVA (p-values described in text, with significance set at p < 0.05).

    Article Snippet: Membranes were blocked with 5% dried skimmed milk/TBS-T (50mM Tris pH 7.6, 150mM NaCl and 0.2% v/v Tween-20) for a minimum of 1-hour prior to overnight incubation at 4°C with primary antibodies; MCPH1 (11962–1-AP, Proteintech), BRCA2 (29450–1-AP, Proteintech) and GAPDH (60004–1-Ig, Proteintech).

    Techniques: Transfection, Control, Western Blot, MTS Assay