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anti dap3 antibody  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology anti dap3 antibody
    Anti Dap3 Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+dap3/DAP-3+Antibody/10__1097_slash_js9__0000000000004615-194-14-17
    Average 93 stars, based on 9 article reviews
    anti dap3 antibody - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Transduction:

    Article Title: A GTP-binding adapter protein couples TRAIL receptors to apoptosis-inducing proteins.
    Article Snippet: Apoptosis-inducing tumor necrosis factor (TNF) family receptors recruit the proforms of caspase family cell death proteases to ligand-receptor complexes through interactions with intracellular adapter proteins.. We have found that the GTP-binding protein DAP3 binds directly (with high affinity) to the death domain of TNF-related apoptosis-inducing ligand (TRAIL) receptors, and is required for TRAIL-induced apoptosis.. DAP3 also associates with the pro-caspase-8–binding adapter protein Fas-associated death domain (FADD), and links FADD to the TRAIL receptors DR4 and DR5.

    Article Title: An Inducible Pathway for Degradation of FLIP Protein Sensitizes Tumor Cells to TRAIL-induced Apoptosis
    Article Snippet: Immunoblotting and Immunoprecipitations—Whole cell lysates prepared with RIPA buffer or cytosolic extracts prepared as above were subjected to SDS-PAGE and transferred to nitrocellulose membranes (Bio-Rad). .. Immunoblotting was performed with the following antibodies: anti-caspase 8 at 1:3000 (v/v) (21) or at 1:1000 from Alexis; antiPARP (BD PharMingen, La Jolla, CA) at 1:1000; anti-FLIP (NF-6) at 1:20 (27); anti-DR5 (Alexis) at 1:500; anti-DR4 (Millennium, Boston, MA) at 1:500; anti-RIP (BD PharMingen) at 1:200; anti-PPAR (Santa Cruz Biotechnology Inc.) at 1:200; anti-TRADD (Santa Cruz Biotechnology Inc.) at 1:250; anti-FADD (BD PharMingen) 1:1000; anti-DcR1 (ProSci Inc., Poway, CA) at 1:500; anti-DcR2 (Calbiochem) at 1:1000; anti-DAP3 (Transduction Laboratories, San Diego, CA) at 1:500; antiubiquitin (Santa Cruz Biotechnology Inc.) at 1:200, and anti- -tubulin (Sigma) at 1:1000 in 0.05% Tween/Tris-buffered saline (T-TBS) blocking buffer containing 5% nonfat skim milk for 1–3 h at room temperature, followed by washing with T-TBS for 30 min. .. Goat anti-rabbit or antimouse IgGs coupled with horseradish peroxidase (Bio-Rad) were used as secondary antibodies at 1:3000 (v/v).

    Western Blot:

    Article Title: An Inducible Pathway for Degradation of FLIP Protein Sensitizes Tumor Cells to TRAIL-induced Apoptosis
    Article Snippet: Immunoblotting and Immunoprecipitations—Whole cell lysates prepared with RIPA buffer or cytosolic extracts prepared as above were subjected to SDS-PAGE and transferred to nitrocellulose membranes (Bio-Rad). .. Immunoblotting was performed with the following antibodies: anti-caspase 8 at 1:3000 (v/v) (21) or at 1:1000 from Alexis; antiPARP (BD PharMingen, La Jolla, CA) at 1:1000; anti-FLIP (NF-6) at 1:20 (27); anti-DR5 (Alexis) at 1:500; anti-DR4 (Millennium, Boston, MA) at 1:500; anti-RIP (BD PharMingen) at 1:200; anti-PPAR (Santa Cruz Biotechnology Inc.) at 1:200; anti-TRADD (Santa Cruz Biotechnology Inc.) at 1:250; anti-FADD (BD PharMingen) 1:1000; anti-DcR1 (ProSci Inc., Poway, CA) at 1:500; anti-DcR2 (Calbiochem) at 1:1000; anti-DAP3 (Transduction Laboratories, San Diego, CA) at 1:500; antiubiquitin (Santa Cruz Biotechnology Inc.) at 1:200, and anti- -tubulin (Sigma) at 1:1000 in 0.05% Tween/Tris-buffered saline (T-TBS) blocking buffer containing 5% nonfat skim milk for 1–3 h at room temperature, followed by washing with T-TBS for 30 min. .. Goat anti-rabbit or antimouse IgGs coupled with horseradish peroxidase (Bio-Rad) were used as secondary antibodies at 1:3000 (v/v).

    Saline:

    Article Title: An Inducible Pathway for Degradation of FLIP Protein Sensitizes Tumor Cells to TRAIL-induced Apoptosis
    Article Snippet: Immunoblotting and Immunoprecipitations—Whole cell lysates prepared with RIPA buffer or cytosolic extracts prepared as above were subjected to SDS-PAGE and transferred to nitrocellulose membranes (Bio-Rad). .. Immunoblotting was performed with the following antibodies: anti-caspase 8 at 1:3000 (v/v) (21) or at 1:1000 from Alexis; antiPARP (BD PharMingen, La Jolla, CA) at 1:1000; anti-FLIP (NF-6) at 1:20 (27); anti-DR5 (Alexis) at 1:500; anti-DR4 (Millennium, Boston, MA) at 1:500; anti-RIP (BD PharMingen) at 1:200; anti-PPAR (Santa Cruz Biotechnology Inc.) at 1:200; anti-TRADD (Santa Cruz Biotechnology Inc.) at 1:250; anti-FADD (BD PharMingen) 1:1000; anti-DcR1 (ProSci Inc., Poway, CA) at 1:500; anti-DcR2 (Calbiochem) at 1:1000; anti-DAP3 (Transduction Laboratories, San Diego, CA) at 1:500; antiubiquitin (Santa Cruz Biotechnology Inc.) at 1:200, and anti- -tubulin (Sigma) at 1:1000 in 0.05% Tween/Tris-buffered saline (T-TBS) blocking buffer containing 5% nonfat skim milk for 1–3 h at room temperature, followed by washing with T-TBS for 30 min. .. Goat anti-rabbit or antimouse IgGs coupled with horseradish peroxidase (Bio-Rad) were used as secondary antibodies at 1:3000 (v/v).

    Blocking Assay:

    Article Title: An Inducible Pathway for Degradation of FLIP Protein Sensitizes Tumor Cells to TRAIL-induced Apoptosis
    Article Snippet: Immunoblotting and Immunoprecipitations—Whole cell lysates prepared with RIPA buffer or cytosolic extracts prepared as above were subjected to SDS-PAGE and transferred to nitrocellulose membranes (Bio-Rad). .. Immunoblotting was performed with the following antibodies: anti-caspase 8 at 1:3000 (v/v) (21) or at 1:1000 from Alexis; antiPARP (BD PharMingen, La Jolla, CA) at 1:1000; anti-FLIP (NF-6) at 1:20 (27); anti-DR5 (Alexis) at 1:500; anti-DR4 (Millennium, Boston, MA) at 1:500; anti-RIP (BD PharMingen) at 1:200; anti-PPAR (Santa Cruz Biotechnology Inc.) at 1:200; anti-TRADD (Santa Cruz Biotechnology Inc.) at 1:250; anti-FADD (BD PharMingen) 1:1000; anti-DcR1 (ProSci Inc., Poway, CA) at 1:500; anti-DcR2 (Calbiochem) at 1:1000; anti-DAP3 (Transduction Laboratories, San Diego, CA) at 1:500; antiubiquitin (Santa Cruz Biotechnology Inc.) at 1:200, and anti- -tubulin (Sigma) at 1:1000 in 0.05% Tween/Tris-buffered saline (T-TBS) blocking buffer containing 5% nonfat skim milk for 1–3 h at room temperature, followed by washing with T-TBS for 30 min. .. Goat anti-rabbit or antimouse IgGs coupled with horseradish peroxidase (Bio-Rad) were used as secondary antibodies at 1:3000 (v/v).

    Clone Assay:

    Article Title: Cathepsin D protects human neuroblastoma cells from doxorubicin-induced cell death.
    Article Snippet: .. The following antibodies were used: mouse monoclonal anti-cathepsin D (clone 49), anti-DAP3 (clone 10) and rabbit polyclonal anti-phospho-Akt S-473 (BD Bioscience, Heidelberg, Germany); anti-b-Actin (clone AC-15) (Sigma); anti-MYCN (clone B8.4.B), anti-a-Tubulin (clone B-7) and antiP53 (clone DO-1) (Santa Cruz Biotechnology, Santa Cruz, CA); rabbit polyclonal anti-phospho-Bcl-2 S-70 (Cell Signaling, Danvers, MA) and anti-p21/ WAF1/Cip1, pooled mouse monoclonal IgGs from clones CP36 and CP74 (Upstate, Millipore, Schwalbach, Germany). ..



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    ABclonal Biotechnology dap3
    Figure 5. Excessive farnesylation of <t>Dap3</t> in Ggps1-KD cells is responsible for impaired mitochondrial function. A, schematic of the screening of prenylated proteins in mitochondria of Ggps1-KD cells in vitro. Protein prenylation was assessed by immunoblotting. B and C, aqueous phase-localized and detergent phase-localized candidate proteins in mitochondrial components of control and Ggps1-KD cells were obtained via Triton X-114 extraction and analyzed by immunoblotting. Assays were performed in 293T cells (B) and Aml12 cells (C). Hsp60 served as mitochondrial markers. M: mitochondria, C: cytosol, D: detergent phase, A: aqueous phase. The experiments were repeated three times. D and E, oxygen consumption rates (OCRs) and maximal respiration in Aml12 cells were detected with an XF Cell Mito Stress Test. We cultured Aml12 cells transfected with vector, Dap3-WT, or Dap3-C363S mutant for 48 h with or without 10 μM DGBP treatment for 24 h. DGBP was used to inhibit Ggps1 activity. (n = 3, **p < 0.01 and ***p < 0.001). The experiments were repeated three times. **p < 0.01, ***p < 0.001, compared with the WT or control by Student’s t test. The data represent the mean ± SEM. See also Table S3. DGBP, digeranyl bisphosphonate; Ggps1, geranylgeranyl diphosphate synthase1.
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    Santa Cruz Biotechnology human dap3 ribozyme transgene
    Figure 1. IHC staining for the <t>DAP3</t> and DELE1 in colon cancer tissues (n=52) and the adjacent tissues (n=62). (A) DAP3 expression and (B) DELE1 expres‑ sion in adjacent normal tissue, T3 and T4 colon cancer tissue with the magnification of x10 and x40, respectively. (C and D) Box plot presenting the differential (C) DAP3 and (D) DELE1 expression in adjacent tissue, early stage, and the advanced stage of colon cancer. *P<0.05, **P<0.01 and ***P<0.001. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1.
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    Image Search Results


    Figure 5. Excessive farnesylation of Dap3 in Ggps1-KD cells is responsible for impaired mitochondrial function. A, schematic of the screening of prenylated proteins in mitochondria of Ggps1-KD cells in vitro. Protein prenylation was assessed by immunoblotting. B and C, aqueous phase-localized and detergent phase-localized candidate proteins in mitochondrial components of control and Ggps1-KD cells were obtained via Triton X-114 extraction and analyzed by immunoblotting. Assays were performed in 293T cells (B) and Aml12 cells (C). Hsp60 served as mitochondrial markers. M: mitochondria, C: cytosol, D: detergent phase, A: aqueous phase. The experiments were repeated three times. D and E, oxygen consumption rates (OCRs) and maximal respiration in Aml12 cells were detected with an XF Cell Mito Stress Test. We cultured Aml12 cells transfected with vector, Dap3-WT, or Dap3-C363S mutant for 48 h with or without 10 μM DGBP treatment for 24 h. DGBP was used to inhibit Ggps1 activity. (n = 3, **p < 0.01 and ***p < 0.001). The experiments were repeated three times. **p < 0.01, ***p < 0.001, compared with the WT or control by Student’s t test. The data represent the mean ± SEM. See also Table S3. DGBP, digeranyl bisphosphonate; Ggps1, geranylgeranyl diphosphate synthase1.

    Journal: The Journal of biological chemistry

    Article Title: Oocytes orchestrate protein prenylation for mitochondrial function through selective inactivation of cholesterol biosynthesis in murine species.

    doi: 10.1016/j.jbc.2023.105183

    Figure Lengend Snippet: Figure 5. Excessive farnesylation of Dap3 in Ggps1-KD cells is responsible for impaired mitochondrial function. A, schematic of the screening of prenylated proteins in mitochondria of Ggps1-KD cells in vitro. Protein prenylation was assessed by immunoblotting. B and C, aqueous phase-localized and detergent phase-localized candidate proteins in mitochondrial components of control and Ggps1-KD cells were obtained via Triton X-114 extraction and analyzed by immunoblotting. Assays were performed in 293T cells (B) and Aml12 cells (C). Hsp60 served as mitochondrial markers. M: mitochondria, C: cytosol, D: detergent phase, A: aqueous phase. The experiments were repeated three times. D and E, oxygen consumption rates (OCRs) and maximal respiration in Aml12 cells were detected with an XF Cell Mito Stress Test. We cultured Aml12 cells transfected with vector, Dap3-WT, or Dap3-C363S mutant for 48 h with or without 10 μM DGBP treatment for 24 h. DGBP was used to inhibit Ggps1 activity. (n = 3, **p < 0.01 and ***p < 0.001). The experiments were repeated three times. **p < 0.01, ***p < 0.001, compared with the WT or control by Student’s t test. The data represent the mean ± SEM. See also Table S3. DGBP, digeranyl bisphosphonate; Ggps1, geranylgeranyl diphosphate synthase1.

    Article Snippet: The immunoblots were blocked with 5% nonfat milk solution and incubated overnight at 4 C with primary antibodies against Ggps1 (1:400, Thermo Fisher), Rap1A (1:400, Santa Cruz), CYTB (1:1000, Proteintech), ND5 (1:1000, Proteintech), MTCO1 (1:1000, Proteintech), Tubulin (1:1000, Proteintech), β-Actin (1:1000, Proteintech), LC3 (1:1000, Proteintech), Rab7 (1:500, Santa Cruz), Rac1 (1:400, Santa Cruz), Rhoa (1:400, Santa Cruz), CLPB (1:1000, Abclonal), ABCB7 (1:1000, Abclonal), DAP3 (1:1000, Abclonal, GPD2 (1:1000, Abcam,), and HSP60 (1:1000, Proteintech).

    Techniques: In Vitro, Western Blot, Control, Extraction, Cell Culture, Transfection, Plasmid Preparation, Mutagenesis, Activity Assay

    Figure 1. IHC staining for the DAP3 and DELE1 in colon cancer tissues (n=52) and the adjacent tissues (n=62). (A) DAP3 expression and (B) DELE1 expres‑ sion in adjacent normal tissue, T3 and T4 colon cancer tissue with the magnification of x10 and x40, respectively. (C and D) Box plot presenting the differential (C) DAP3 and (D) DELE1 expression in adjacent tissue, early stage, and the advanced stage of colon cancer. *P<0.05, **P<0.01 and ***P<0.001. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1.

    Journal: International journal of oncology

    Article Title: Death associated protein‑3 (DAP3) and DAP3 binding cell death enhancer‑1 (DELE1) in human colorectal cancer, and their impacts on clinical outcome and chemoresistance.

    doi: 10.3892/ijo.2022.5455

    Figure Lengend Snippet: Figure 1. IHC staining for the DAP3 and DELE1 in colon cancer tissues (n=52) and the adjacent tissues (n=62). (A) DAP3 expression and (B) DELE1 expres‑ sion in adjacent normal tissue, T3 and T4 colon cancer tissue with the magnification of x10 and x40, respectively. (C and D) Box plot presenting the differential (C) DAP3 and (D) DELE1 expression in adjacent tissue, early stage, and the advanced stage of colon cancer. *P<0.05, **P<0.01 and ***P<0.001. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1.

    Article Snippet: Anti‐human DELE1 siRNA was purchased from Santa Cruz Biotechnologies, Inc. An anti‐human DAP3 ribozyme transgene that was specifically used to target and knockdown human DAP3 was prepared as previously reported (12).

    Techniques: Immunohistochemistry, Expressing, Binding Assay

    Figure 2. Kaplan‑Meier survival analyses showed correlations between overall survival, disease‑free survival, distant metastasis‑free survival, recurrence‑free survival and altered expression of DAP3, DELE1 and DAP3/DELE1 ratio. P‑values shown are from the log ranked test. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1.

    Journal: International journal of oncology

    Article Title: Death associated protein‑3 (DAP3) and DAP3 binding cell death enhancer‑1 (DELE1) in human colorectal cancer, and their impacts on clinical outcome and chemoresistance.

    doi: 10.3892/ijo.2022.5455

    Figure Lengend Snippet: Figure 2. Kaplan‑Meier survival analyses showed correlations between overall survival, disease‑free survival, distant metastasis‑free survival, recurrence‑free survival and altered expression of DAP3, DELE1 and DAP3/DELE1 ratio. P‑values shown are from the log ranked test. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1.

    Article Snippet: Anti‐human DELE1 siRNA was purchased from Santa Cruz Biotechnologies, Inc. An anti‐human DAP3 ribozyme transgene that was specifically used to target and knockdown human DAP3 was prepared as previously reported (12).

    Techniques: Expressing, Binding Assay

    Figure 3. Response to chemotherapy with differential transcript DELE1 and DAP3 respectively. This was based on the public database (www.rocplot.com). Shown in the figure is the median of the respective group. *P<0.05 by Mann‑Whitney U test. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1.

    Journal: International journal of oncology

    Article Title: Death associated protein‑3 (DAP3) and DAP3 binding cell death enhancer‑1 (DELE1) in human colorectal cancer, and their impacts on clinical outcome and chemoresistance.

    doi: 10.3892/ijo.2022.5455

    Figure Lengend Snippet: Figure 3. Response to chemotherapy with differential transcript DELE1 and DAP3 respectively. This was based on the public database (www.rocplot.com). Shown in the figure is the median of the respective group. *P<0.05 by Mann‑Whitney U test. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1.

    Article Snippet: Anti‐human DELE1 siRNA was purchased from Santa Cruz Biotechnologies, Inc. An anti‐human DAP3 ribozyme transgene that was specifically used to target and knockdown human DAP3 was prepared as previously reported (12).

    Techniques: Mann-Whitney U-Test, Binding Assay

    Figure 4. Correlation between DAP3 and DELE1 with angiogenesis biomarkers. (A and B) Correlation efficiency between DAP3 and angiogenesis markers in The Cancer Genome Atlas‑COAD cohort was presented in (A) heatmap (A) and (B) scatter plots. (C and D) Association between DELE1 and angiogenesis biomarkers was revealed in (C) heatmap and (D) scatter plots. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1. **P<0.01.

    Journal: International journal of oncology

    Article Title: Death associated protein‑3 (DAP3) and DAP3 binding cell death enhancer‑1 (DELE1) in human colorectal cancer, and their impacts on clinical outcome and chemoresistance.

    doi: 10.3892/ijo.2022.5455

    Figure Lengend Snippet: Figure 4. Correlation between DAP3 and DELE1 with angiogenesis biomarkers. (A and B) Correlation efficiency between DAP3 and angiogenesis markers in The Cancer Genome Atlas‑COAD cohort was presented in (A) heatmap (A) and (B) scatter plots. (C and D) Association between DELE1 and angiogenesis biomarkers was revealed in (C) heatmap and (D) scatter plots. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1. **P<0.01.

    Article Snippet: Anti‐human DELE1 siRNA was purchased from Santa Cruz Biotechnologies, Inc. An anti‐human DAP3 ribozyme transgene that was specifically used to target and knockdown human DAP3 was prepared as previously reported (12).

    Techniques: Binding Assay

    Figure 5. Validation of the DAP3 and DELE1 knockdown in RKO cells by quantitative PCR gene transcript analysis. Left panel: Expression of DAP3 in the cell models. The levels of expression in wild type, control transfection (control plasmid and control siRNA), DAP3 knockdown, DELE1 knockdown and DAP3/DELE1 dual knockdown cells were compared. Control transfections resulted in minor and statistically insignificant changes of DAP3 when compared with wild type cells (P>0.05) Right panel: Expression of DELE1 in the cell models. The levels of expression in wild type, control transfection (control plasmid and control siRNA), DELE1 knockdown and DAP3/DELE1 dual knockdown cells were compared. Control transfections resulted in minor and statisti‑ cally insignificant changes of DELE1 when compared with wild type cells (P>0.05). Values presented in the figure are mean and standard deviation. Error bars represent standard deviation. **P<0.01 vs. RKO wild type cells, ΔΔP<0.001 vs. RKO‑control‑plasmid cells and ##P<0.01 VS RKO‑control‑siRNA cells. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1; siRNA, small interfering RNA.

    Journal: International journal of oncology

    Article Title: Death associated protein‑3 (DAP3) and DAP3 binding cell death enhancer‑1 (DELE1) in human colorectal cancer, and their impacts on clinical outcome and chemoresistance.

    doi: 10.3892/ijo.2022.5455

    Figure Lengend Snippet: Figure 5. Validation of the DAP3 and DELE1 knockdown in RKO cells by quantitative PCR gene transcript analysis. Left panel: Expression of DAP3 in the cell models. The levels of expression in wild type, control transfection (control plasmid and control siRNA), DAP3 knockdown, DELE1 knockdown and DAP3/DELE1 dual knockdown cells were compared. Control transfections resulted in minor and statistically insignificant changes of DAP3 when compared with wild type cells (P>0.05) Right panel: Expression of DELE1 in the cell models. The levels of expression in wild type, control transfection (control plasmid and control siRNA), DELE1 knockdown and DAP3/DELE1 dual knockdown cells were compared. Control transfections resulted in minor and statisti‑ cally insignificant changes of DELE1 when compared with wild type cells (P>0.05). Values presented in the figure are mean and standard deviation. Error bars represent standard deviation. **P<0.01 vs. RKO wild type cells, ΔΔP<0.001 vs. RKO‑control‑plasmid cells and ##P<0.01 VS RKO‑control‑siRNA cells. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1; siRNA, small interfering RNA.

    Article Snippet: Anti‐human DELE1 siRNA was purchased from Santa Cruz Biotechnologies, Inc. An anti‐human DAP3 ribozyme transgene that was specifically used to target and knockdown human DAP3 was prepared as previously reported (12).

    Techniques: Biomarker Discovery, Knockdown, Real-time Polymerase Chain Reaction, Expressing, Control, Transfection, Plasmid Preparation, Standard Deviation, Binding Assay, Small Interfering RNA

    Figure 7. Metabolic of colorectal cancer cells following DAP3 and DELE1 knockdown. (A) Concentrations of extracellular glucose in different RKO cells were determined by luminescence measurement. (B) NAD(P)H measurements quantified by luminescence in different RKO cells. (C) Differential extracellular lactate expression and the ratio in different RKO cells. (D) NO2 Standard curve and measurements of NO2 in different RKO cells. Error bar stands standard error of means. *P<0.05 and **P<0.01 by Student's t‑test. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1.

    Journal: International journal of oncology

    Article Title: Death associated protein‑3 (DAP3) and DAP3 binding cell death enhancer‑1 (DELE1) in human colorectal cancer, and their impacts on clinical outcome and chemoresistance.

    doi: 10.3892/ijo.2022.5455

    Figure Lengend Snippet: Figure 7. Metabolic of colorectal cancer cells following DAP3 and DELE1 knockdown. (A) Concentrations of extracellular glucose in different RKO cells were determined by luminescence measurement. (B) NAD(P)H measurements quantified by luminescence in different RKO cells. (C) Differential extracellular lactate expression and the ratio in different RKO cells. (D) NO2 Standard curve and measurements of NO2 in different RKO cells. Error bar stands standard error of means. *P<0.05 and **P<0.01 by Student's t‑test. DAP3, death associated protein‑3; DELE1, DAP3 binding cell death enhancer‑1.

    Article Snippet: Anti‐human DELE1 siRNA was purchased from Santa Cruz Biotechnologies, Inc. An anti‐human DAP3 ribozyme transgene that was specifically used to target and knockdown human DAP3 was prepared as previously reported (12).

    Techniques: Knockdown, Expressing, Binding Assay