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Gene mutations, expression correlations and promoter methylation levels of <t>ARID1A</t> , ARID1B and ARID2 in COAD. (A) Genetic alterations of ARID1A , ARID1B and ARID2 in patients from TCGA-COAD cohort, analyzed using the Cancer Virtual Cohort Discovery Analysis Platform. Expression correlations between (B) ARID1A and ARID1B , (C) ARID1A and ARID2 and (D) ARID1B and ARID2 in TCGA-COAD cohort, analyzed via the Gene Expression Profiling Interactive Analysis 2 platform. The promoter methylation level of (E) ARID1A , (F) ARID1B and (G) ARID2 in TCGA-COAD samples, analyzed via The University of ALabama at Birmingham CANcer data analysis portal. ** P<0.01. ARID, AT-rich interactive domain; COAD, colon adenocarcinoma; TCGA, The Cancer Genome Atlas.
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<t>ARID1A</t> protein expression in the empty vector control and ARID1A-overexpressing cells. (A) Western blot images of ARID1A and GAPDH (loading control). (B) Band intensity of ARID1A relative to GAPDH. The bar graph represents the mean ± standard deviation (n=3 per group). *P<0.05. ARID1A, AT-rich interacting domain-containing protein 1A; O/E, overexpression; MW, molecular weight.
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Figure 1. Immunohistochemical staining for <t>ARID1A.</t> (A) Preserved expression; (B) Loss of expres- sion. Magnification: 200×.
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Image Search Results


Gene mutations, expression correlations and promoter methylation levels of ARID1A , ARID1B and ARID2 in COAD. (A) Genetic alterations of ARID1A , ARID1B and ARID2 in patients from TCGA-COAD cohort, analyzed using the Cancer Virtual Cohort Discovery Analysis Platform. Expression correlations between (B) ARID1A and ARID1B , (C) ARID1A and ARID2 and (D) ARID1B and ARID2 in TCGA-COAD cohort, analyzed via the Gene Expression Profiling Interactive Analysis 2 platform. The promoter methylation level of (E) ARID1A , (F) ARID1B and (G) ARID2 in TCGA-COAD samples, analyzed via The University of ALabama at Birmingham CANcer data analysis portal. ** P<0.01. ARID, AT-rich interactive domain; COAD, colon adenocarcinoma; TCGA, The Cancer Genome Atlas.

Journal: Biomedical Reports

Article Title: Relationship between the protein expression of ARID1A, ARID1B and ARID2 with the clinicopathological characteristics of colorectal cancer

doi: 10.3892/br.2025.1997

Figure Lengend Snippet: Gene mutations, expression correlations and promoter methylation levels of ARID1A , ARID1B and ARID2 in COAD. (A) Genetic alterations of ARID1A , ARID1B and ARID2 in patients from TCGA-COAD cohort, analyzed using the Cancer Virtual Cohort Discovery Analysis Platform. Expression correlations between (B) ARID1A and ARID1B , (C) ARID1A and ARID2 and (D) ARID1B and ARID2 in TCGA-COAD cohort, analyzed via the Gene Expression Profiling Interactive Analysis 2 platform. The promoter methylation level of (E) ARID1A , (F) ARID1B and (G) ARID2 in TCGA-COAD samples, analyzed via The University of ALabama at Birmingham CANcer data analysis portal. ** P<0.01. ARID, AT-rich interactive domain; COAD, colon adenocarcinoma; TCGA, The Cancer Genome Atlas.

Article Snippet: To assess the expression of the ARID proteins, IHC was performed using the following specific antibodies: Anti-ARID1A rabbit polyclonal antibody (1:400; cat. no. HPA005456; MilliporeSigma), anti-ARID1B mouse monoclonal antibody (1:200; cat. no. ab57461; Abcam) and anti-ARID2 rabbit polyclonal antibody (1:250; cat. no. ab113283; Abcam).

Techniques: Expressing, Methylation, Gene Expression

ARID1A, ARID1B and ARID2 protein expression in colorectal cancer tissues. Immunohistochemistry of (A) ARID1A, (B) ARID1B and (C) ARID2 proteins in the adjacent non-cancerous area compared with the cancerous area. ARID protein staining appears brown (magnification, x400; scale bar, 20 µm). The H-score of (D) ARID1A, (E) ARID1B and (F) ARID2 protein expression in the non-cancerous area (black bar) compared with the cancerous area (white bar). The data are presented as the mean ± SEM and analyzed by the Mann-Whitney U test. (G) Distribution of ARID1A, ARID1B and ARID2 expression categorization in adjacent non-cancerous and cancerous areas. Expression is classified as low or high depending on the median H-score. ARID1A cut-off, 164; ARID1B cut-off, 100; ARID2 cut-off, 78. * P<0.05, ** P<0.01 and *** P<0.001. ARID, AT-rich interactive domain; H-score, histoscore; SEM, standard error of the mean; NA, adjacent non-cancerous area; CA, cancerous area.

Journal: Biomedical Reports

Article Title: Relationship between the protein expression of ARID1A, ARID1B and ARID2 with the clinicopathological characteristics of colorectal cancer

doi: 10.3892/br.2025.1997

Figure Lengend Snippet: ARID1A, ARID1B and ARID2 protein expression in colorectal cancer tissues. Immunohistochemistry of (A) ARID1A, (B) ARID1B and (C) ARID2 proteins in the adjacent non-cancerous area compared with the cancerous area. ARID protein staining appears brown (magnification, x400; scale bar, 20 µm). The H-score of (D) ARID1A, (E) ARID1B and (F) ARID2 protein expression in the non-cancerous area (black bar) compared with the cancerous area (white bar). The data are presented as the mean ± SEM and analyzed by the Mann-Whitney U test. (G) Distribution of ARID1A, ARID1B and ARID2 expression categorization in adjacent non-cancerous and cancerous areas. Expression is classified as low or high depending on the median H-score. ARID1A cut-off, 164; ARID1B cut-off, 100; ARID2 cut-off, 78. * P<0.05, ** P<0.01 and *** P<0.001. ARID, AT-rich interactive domain; H-score, histoscore; SEM, standard error of the mean; NA, adjacent non-cancerous area; CA, cancerous area.

Article Snippet: To assess the expression of the ARID proteins, IHC was performed using the following specific antibodies: Anti-ARID1A rabbit polyclonal antibody (1:400; cat. no. HPA005456; MilliporeSigma), anti-ARID1B mouse monoclonal antibody (1:200; cat. no. ab57461; Abcam) and anti-ARID2 rabbit polyclonal antibody (1:250; cat. no. ab113283; Abcam).

Techniques: Expressing, Immunohistochemistry, Staining, MANN-WHITNEY

Expression correlations of ARID1A, ARID1B and ARID2 protein in colorectal cancer. Scatterplots showing the relationships between (A) ARID1A and ARID1B, (B) ARID1A and ARID2 and (C) ARID1B and ARID2. (D) Heatmap of Spearman's correlation coefficients among the ARID proteins. * P<0.05. ARID, AT-rich interactive domain; H-score, histoscore.

Journal: Biomedical Reports

Article Title: Relationship between the protein expression of ARID1A, ARID1B and ARID2 with the clinicopathological characteristics of colorectal cancer

doi: 10.3892/br.2025.1997

Figure Lengend Snippet: Expression correlations of ARID1A, ARID1B and ARID2 protein in colorectal cancer. Scatterplots showing the relationships between (A) ARID1A and ARID1B, (B) ARID1A and ARID2 and (C) ARID1B and ARID2. (D) Heatmap of Spearman's correlation coefficients among the ARID proteins. * P<0.05. ARID, AT-rich interactive domain; H-score, histoscore.

Article Snippet: To assess the expression of the ARID proteins, IHC was performed using the following specific antibodies: Anti-ARID1A rabbit polyclonal antibody (1:400; cat. no. HPA005456; MilliporeSigma), anti-ARID1B mouse monoclonal antibody (1:200; cat. no. ab57461; Abcam) and anti-ARID2 rabbit polyclonal antibody (1:250; cat. no. ab113283; Abcam).

Techniques: Expressing

Relationship between ARID1A, ARID1B and ARID2 protein expression and the survival outcomes of patients with CRC. The 5-year progression-free survival outcomes based on the expression status of (A) ARID1A, (B) ARID1B and (C) ARID2 in patients with CRC (n=63), analyzed using log-rank test. Overall survival based on the expression status of (D) ARID1A, (E) ARID1B and (F) ARID2 in patients with CRC, analyzed using the KM plotter database. The KM plots for overall survival were generated directly by the KM plotter tool without any additional statistical analysis or modification. A late-stage crossover was observed in the survival curves, as provided by the tool. * P<0.05. ARID, AT-rich interactive domain; CRC, colorectal cancer; KM, Kaplan-Meier.

Journal: Biomedical Reports

Article Title: Relationship between the protein expression of ARID1A, ARID1B and ARID2 with the clinicopathological characteristics of colorectal cancer

doi: 10.3892/br.2025.1997

Figure Lengend Snippet: Relationship between ARID1A, ARID1B and ARID2 protein expression and the survival outcomes of patients with CRC. The 5-year progression-free survival outcomes based on the expression status of (A) ARID1A, (B) ARID1B and (C) ARID2 in patients with CRC (n=63), analyzed using log-rank test. Overall survival based on the expression status of (D) ARID1A, (E) ARID1B and (F) ARID2 in patients with CRC, analyzed using the KM plotter database. The KM plots for overall survival were generated directly by the KM plotter tool without any additional statistical analysis or modification. A late-stage crossover was observed in the survival curves, as provided by the tool. * P<0.05. ARID, AT-rich interactive domain; CRC, colorectal cancer; KM, Kaplan-Meier.

Article Snippet: To assess the expression of the ARID proteins, IHC was performed using the following specific antibodies: Anti-ARID1A rabbit polyclonal antibody (1:400; cat. no. HPA005456; MilliporeSigma), anti-ARID1B mouse monoclonal antibody (1:200; cat. no. ab57461; Abcam) and anti-ARID2 rabbit polyclonal antibody (1:250; cat. no. ab113283; Abcam).

Techniques: Expressing, Generated, Modification

ARID1A protein expression in the empty vector control and ARID1A-overexpressing cells. (A) Western blot images of ARID1A and GAPDH (loading control). (B) Band intensity of ARID1A relative to GAPDH. The bar graph represents the mean ± standard deviation (n=3 per group). *P<0.05. ARID1A, AT-rich interacting domain-containing protein 1A; O/E, overexpression; MW, molecular weight.

Journal: Oncology Letters

Article Title: Proteomic insights into the regulatory function of ARID1A in colon cancer cells

doi: 10.3892/ol.2024.14525

Figure Lengend Snippet: ARID1A protein expression in the empty vector control and ARID1A-overexpressing cells. (A) Western blot images of ARID1A and GAPDH (loading control). (B) Band intensity of ARID1A relative to GAPDH. The bar graph represents the mean ± standard deviation (n=3 per group). *P<0.05. ARID1A, AT-rich interacting domain-containing protein 1A; O/E, overexpression; MW, molecular weight.

Article Snippet: The membrane was incubated with 5% skimmed milk in PBS at 25°C for 1 h. Subsequently, it was incubated with rabbit polyclonal anti-ARID1A (1:1,000; cat. no. HPA005456; Sigma-Aldrich; Merck KGaA), rabbit monoclonal anti-c-Myc (1:1,000; cat. no. 5605; Cell Signaling Technology, Inc.), rabbit monoclonal anti-T cell factor (TCF)1/7 (1:1,000; cat. no. 2203; Cell Signaling Technology, Inc.), rabbit monoclonal anti-cyclin D1 (1:1,000; cat. no. 2978; Cell Signaling Technology, Inc.), rabbit polyclonal anti-zinc and ring finger 3 (ZNRF3; 1:1,000; cat. no. DF14289; Affinity Biosciences), or mouse monoclonal anti-GAPDH (1:5,000; cat. no. ab8245; Abcam) antibodies at 4°C overnight.

Techniques: Expressing, Plasmid Preparation, Control, Western Blot, Standard Deviation, Over Expression, Molecular Weight

Involvement of ARID1A and altered proteins in the Wnt signaling pathway. (A) Wnt signaling pathway information generated using Kyoto Encyclopedia of Genes and Genomes (hsa04310). The pathway is illustrated using data from the KEGG database ( https://www.genome.jp/pathway/hsa04310 ) . Red boxes indicate differentially altered proteins. (B) Western blot images for c-Myc, TCF1/TCF7 and cyclin D1, with GAPDH as the loading control. (C) Band intensity of proteins relative to GAPDH. The bar graph represents the mean ± standard deviation (n=3 per group). *P<0.05. ARID1A, AT-rich interacting domain-containing protein 1A; TCF, T cell factor; O/E, overexpression; MW, molecular weight.

Journal: Oncology Letters

Article Title: Proteomic insights into the regulatory function of ARID1A in colon cancer cells

doi: 10.3892/ol.2024.14525

Figure Lengend Snippet: Involvement of ARID1A and altered proteins in the Wnt signaling pathway. (A) Wnt signaling pathway information generated using Kyoto Encyclopedia of Genes and Genomes (hsa04310). The pathway is illustrated using data from the KEGG database ( https://www.genome.jp/pathway/hsa04310 ) . Red boxes indicate differentially altered proteins. (B) Western blot images for c-Myc, TCF1/TCF7 and cyclin D1, with GAPDH as the loading control. (C) Band intensity of proteins relative to GAPDH. The bar graph represents the mean ± standard deviation (n=3 per group). *P<0.05. ARID1A, AT-rich interacting domain-containing protein 1A; TCF, T cell factor; O/E, overexpression; MW, molecular weight.

Article Snippet: The membrane was incubated with 5% skimmed milk in PBS at 25°C for 1 h. Subsequently, it was incubated with rabbit polyclonal anti-ARID1A (1:1,000; cat. no. HPA005456; Sigma-Aldrich; Merck KGaA), rabbit monoclonal anti-c-Myc (1:1,000; cat. no. 5605; Cell Signaling Technology, Inc.), rabbit monoclonal anti-T cell factor (TCF)1/7 (1:1,000; cat. no. 2203; Cell Signaling Technology, Inc.), rabbit monoclonal anti-cyclin D1 (1:1,000; cat. no. 2978; Cell Signaling Technology, Inc.), rabbit polyclonal anti-zinc and ring finger 3 (ZNRF3; 1:1,000; cat. no. DF14289; Affinity Biosciences), or mouse monoclonal anti-GAPDH (1:5,000; cat. no. ab8245; Abcam) antibodies at 4°C overnight.

Techniques: Generated, Western Blot, Control, Standard Deviation, Over Expression, Molecular Weight

Association between ARID1A and altered proteins involved in the Wnt signaling pathway. (A) Interaction network of ARID1A and altered proteins involved in the Wnt signaling pathway constructed using GeneMANIA. (B) Heatmap of the HR of TCF7L1 and ZNRF3 for the overall survival of patients with COAD, created using GEPIA2. The framed block indicates a significant prognostic value. (C) Kaplan-Meier curve for overall survival of patients with COAD with different levels of ZNRF3 expression, plotted using GEPIA2. (D) Correlation between the expression of ARID1A and ZNRF3 in COAD, analyzed using GEPIA2. ARID1A, AT-rich interacting domain-containing protein 1A; TCF7L1, transcription factor 7 like 1; ZNRF3, zinc and ring finger 3; COAD, colon adenocarcinoma; GEPIA2, Gene Expression Profiling Interactive Analysis 2; HR, hazard ratio; TPM, transcripts per million.

Journal: Oncology Letters

Article Title: Proteomic insights into the regulatory function of ARID1A in colon cancer cells

doi: 10.3892/ol.2024.14525

Figure Lengend Snippet: Association between ARID1A and altered proteins involved in the Wnt signaling pathway. (A) Interaction network of ARID1A and altered proteins involved in the Wnt signaling pathway constructed using GeneMANIA. (B) Heatmap of the HR of TCF7L1 and ZNRF3 for the overall survival of patients with COAD, created using GEPIA2. The framed block indicates a significant prognostic value. (C) Kaplan-Meier curve for overall survival of patients with COAD with different levels of ZNRF3 expression, plotted using GEPIA2. (D) Correlation between the expression of ARID1A and ZNRF3 in COAD, analyzed using GEPIA2. ARID1A, AT-rich interacting domain-containing protein 1A; TCF7L1, transcription factor 7 like 1; ZNRF3, zinc and ring finger 3; COAD, colon adenocarcinoma; GEPIA2, Gene Expression Profiling Interactive Analysis 2; HR, hazard ratio; TPM, transcripts per million.

Article Snippet: The membrane was incubated with 5% skimmed milk in PBS at 25°C for 1 h. Subsequently, it was incubated with rabbit polyclonal anti-ARID1A (1:1,000; cat. no. HPA005456; Sigma-Aldrich; Merck KGaA), rabbit monoclonal anti-c-Myc (1:1,000; cat. no. 5605; Cell Signaling Technology, Inc.), rabbit monoclonal anti-T cell factor (TCF)1/7 (1:1,000; cat. no. 2203; Cell Signaling Technology, Inc.), rabbit monoclonal anti-cyclin D1 (1:1,000; cat. no. 2978; Cell Signaling Technology, Inc.), rabbit polyclonal anti-zinc and ring finger 3 (ZNRF3; 1:1,000; cat. no. DF14289; Affinity Biosciences), or mouse monoclonal anti-GAPDH (1:5,000; cat. no. ab8245; Abcam) antibodies at 4°C overnight.

Techniques: Construct, Blocking Assay, Expressing

ZNRF3 protein expression in the empty vector control and ARID1A-overexpressing cells. (A) Western blot images of ZNRF3 and GAPDH (loading control) expression. (B) Band intensity of ZNRF3 expression relative to GAPDH. The bar graph represents the mean ± standard deviation (n=3 per group). *P<0.05. ZNRF3, zinc and ring finger 3; ARID1A, AT-rich interacting domain-containing protein 1A; O/E, overexpression; MW, molecular weight.

Journal: Oncology Letters

Article Title: Proteomic insights into the regulatory function of ARID1A in colon cancer cells

doi: 10.3892/ol.2024.14525

Figure Lengend Snippet: ZNRF3 protein expression in the empty vector control and ARID1A-overexpressing cells. (A) Western blot images of ZNRF3 and GAPDH (loading control) expression. (B) Band intensity of ZNRF3 expression relative to GAPDH. The bar graph represents the mean ± standard deviation (n=3 per group). *P<0.05. ZNRF3, zinc and ring finger 3; ARID1A, AT-rich interacting domain-containing protein 1A; O/E, overexpression; MW, molecular weight.

Article Snippet: The membrane was incubated with 5% skimmed milk in PBS at 25°C for 1 h. Subsequently, it was incubated with rabbit polyclonal anti-ARID1A (1:1,000; cat. no. HPA005456; Sigma-Aldrich; Merck KGaA), rabbit monoclonal anti-c-Myc (1:1,000; cat. no. 5605; Cell Signaling Technology, Inc.), rabbit monoclonal anti-T cell factor (TCF)1/7 (1:1,000; cat. no. 2203; Cell Signaling Technology, Inc.), rabbit monoclonal anti-cyclin D1 (1:1,000; cat. no. 2978; Cell Signaling Technology, Inc.), rabbit polyclonal anti-zinc and ring finger 3 (ZNRF3; 1:1,000; cat. no. DF14289; Affinity Biosciences), or mouse monoclonal anti-GAPDH (1:5,000; cat. no. ab8245; Abcam) antibodies at 4°C overnight.

Techniques: Expressing, Plasmid Preparation, Control, Western Blot, Standard Deviation, Over Expression, Molecular Weight

Primer lists and their sequences used in the study

Journal: Journal of Cellular and Molecular Medicine

Article Title: ARID1A downregulation promotes cell proliferation and migration of colon cancer via VIM activation and CDH1 suppression

doi: 10.1111/jcmm.17590

Figure Lengend Snippet: Primer lists and their sequences used in the study

Article Snippet: The membrane was incubated overnight at 4°C with rabbit antibodies against β‐actin (1:1000, Beijing Zhongshan Biotechnology Co., Ltd); ARID1A (1:300, CUSABIO TECHNOLOGY LLC); E‐cadherin Polyclonal antibody, cat on: 20874‐1‐AP; and Vimentin Polyclonal antibody, cat no: 10366‐1‐AP after blocking with 5% non‐fat milk in Tris‐buffered saline containing 0.05%Tween‐20 (1–1000).

Techniques: Sequencing, Negative Control

Identified differentially expressed genes (DEGs)in HCT116‐ARID1A‐wild‐type vs. HCT116‐ARID1A‐knockout (A) Volcano plot of differentially expressed genes (B) Heat map of DEGs in control and knockout groups (C) upper part,KEGG and GO enrichment analysis of differentially upregulated genes. (C) lower part ,KEGG and GO enrichment analysis of differentially downregulated genes

Journal: Journal of Cellular and Molecular Medicine

Article Title: ARID1A downregulation promotes cell proliferation and migration of colon cancer via VIM activation and CDH1 suppression

doi: 10.1111/jcmm.17590

Figure Lengend Snippet: Identified differentially expressed genes (DEGs)in HCT116‐ARID1A‐wild‐type vs. HCT116‐ARID1A‐knockout (A) Volcano plot of differentially expressed genes (B) Heat map of DEGs in control and knockout groups (C) upper part,KEGG and GO enrichment analysis of differentially upregulated genes. (C) lower part ,KEGG and GO enrichment analysis of differentially downregulated genes

Article Snippet: The membrane was incubated overnight at 4°C with rabbit antibodies against β‐actin (1:1000, Beijing Zhongshan Biotechnology Co., Ltd); ARID1A (1:300, CUSABIO TECHNOLOGY LLC); E‐cadherin Polyclonal antibody, cat on: 20874‐1‐AP; and Vimentin Polyclonal antibody, cat no: 10366‐1‐AP after blocking with 5% non‐fat milk in Tris‐buffered saline containing 0.05%Tween‐20 (1–1000).

Techniques: Knock-Out, Control

Expression of EMT‐related markers (VIM) and correlation with ARID1A (A) Vimentin (VIM) overexpression was found in KO cell lines (B) VIM high expression is associated with a poor prognosis in COAD (C) VIM displays high expression in cells with lower ARID1A expression (SW620&RKO) and low expression in cells with a high ARID1A expression (HCT116&LoVo) (D) colon cancer samples were examined for co‐expression of Vimentin and ARID1A (E) GEPIA2 database visualization of the co‐expression of Vimentin and ARID1A in colon cancer tissue.

Journal: Journal of Cellular and Molecular Medicine

Article Title: ARID1A downregulation promotes cell proliferation and migration of colon cancer via VIM activation and CDH1 suppression

doi: 10.1111/jcmm.17590

Figure Lengend Snippet: Expression of EMT‐related markers (VIM) and correlation with ARID1A (A) Vimentin (VIM) overexpression was found in KO cell lines (B) VIM high expression is associated with a poor prognosis in COAD (C) VIM displays high expression in cells with lower ARID1A expression (SW620&RKO) and low expression in cells with a high ARID1A expression (HCT116&LoVo) (D) colon cancer samples were examined for co‐expression of Vimentin and ARID1A (E) GEPIA2 database visualization of the co‐expression of Vimentin and ARID1A in colon cancer tissue.

Article Snippet: The membrane was incubated overnight at 4°C with rabbit antibodies against β‐actin (1:1000, Beijing Zhongshan Biotechnology Co., Ltd); ARID1A (1:300, CUSABIO TECHNOLOGY LLC); E‐cadherin Polyclonal antibody, cat on: 20874‐1‐AP; and Vimentin Polyclonal antibody, cat no: 10366‐1‐AP after blocking with 5% non‐fat milk in Tris‐buffered saline containing 0.05%Tween‐20 (1–1000).

Techniques: Expressing, Over Expression

Expression of EMT‐related marker (CDH1) and correlation with ARID1A (A) CDH1 is downregulated in ARID1A deficient cells (B) shows a Kaplan–Maier result of CDH1 in COAD (C and D) E‐cadherin expression correlates positively with ARID1A expression in COAD

Journal: Journal of Cellular and Molecular Medicine

Article Title: ARID1A downregulation promotes cell proliferation and migration of colon cancer via VIM activation and CDH1 suppression

doi: 10.1111/jcmm.17590

Figure Lengend Snippet: Expression of EMT‐related marker (CDH1) and correlation with ARID1A (A) CDH1 is downregulated in ARID1A deficient cells (B) shows a Kaplan–Maier result of CDH1 in COAD (C and D) E‐cadherin expression correlates positively with ARID1A expression in COAD

Article Snippet: The membrane was incubated overnight at 4°C with rabbit antibodies against β‐actin (1:1000, Beijing Zhongshan Biotechnology Co., Ltd); ARID1A (1:300, CUSABIO TECHNOLOGY LLC); E‐cadherin Polyclonal antibody, cat on: 20874‐1‐AP; and Vimentin Polyclonal antibody, cat no: 10366‐1‐AP after blocking with 5% non‐fat milk in Tris‐buffered saline containing 0.05%Tween‐20 (1–1000).

Techniques: Expressing, Marker

 ARID1A  sequence and mutation profiles in CRC cells used in the research

Journal: Journal of Cellular and Molecular Medicine

Article Title: ARID1A downregulation promotes cell proliferation and migration of colon cancer via VIM activation and CDH1 suppression

doi: 10.1111/jcmm.17590

Figure Lengend Snippet: ARID1A sequence and mutation profiles in CRC cells used in the research

Article Snippet: The membrane was incubated overnight at 4°C with rabbit antibodies against β‐actin (1:1000, Beijing Zhongshan Biotechnology Co., Ltd); ARID1A (1:300, CUSABIO TECHNOLOGY LLC); E‐cadherin Polyclonal antibody, cat on: 20874‐1‐AP; and Vimentin Polyclonal antibody, cat no: 10366‐1‐AP after blocking with 5% non‐fat milk in Tris‐buffered saline containing 0.05%Tween‐20 (1–1000).

Techniques: Sequencing, Mutagenesis, Variant Assay

ARID1A knockdown in HCT116 cell line (A) At 50 nM, 4 μl siRNA‐ARID1A, qPCR demonstrates no change of vimentin and E‐cadherin expression levels in HCT116 after 24 h transfection (B) ARID1A deficiency at 75 nM, 6 μl siRNA‐ARID1A for 24 h activates VIM and suppress CDH1 in HCT116 (C) qPCR results of ARID1A downregulation using 75 nM, 6‐μl siRNA for 48 h showed VIM and CDH1 expression in HCT116. ARID1A silencing altered VIM and E‐cadherin expression (D and E) VIM and CDH1 expression were altered in qPCR results of LS174‐T‐ARID1A knocked down for 24 and 48 h, respectively. ns, Non‐significant; *p < 0.05, **p < 0.001, and ***p < 0.0001

Journal: Journal of Cellular and Molecular Medicine

Article Title: ARID1A downregulation promotes cell proliferation and migration of colon cancer via VIM activation and CDH1 suppression

doi: 10.1111/jcmm.17590

Figure Lengend Snippet: ARID1A knockdown in HCT116 cell line (A) At 50 nM, 4 μl siRNA‐ARID1A, qPCR demonstrates no change of vimentin and E‐cadherin expression levels in HCT116 after 24 h transfection (B) ARID1A deficiency at 75 nM, 6 μl siRNA‐ARID1A for 24 h activates VIM and suppress CDH1 in HCT116 (C) qPCR results of ARID1A downregulation using 75 nM, 6‐μl siRNA for 48 h showed VIM and CDH1 expression in HCT116. ARID1A silencing altered VIM and E‐cadherin expression (D and E) VIM and CDH1 expression were altered in qPCR results of LS174‐T‐ARID1A knocked down for 24 and 48 h, respectively. ns, Non‐significant; *p < 0.05, **p < 0.001, and ***p < 0.0001

Article Snippet: The membrane was incubated overnight at 4°C with rabbit antibodies against β‐actin (1:1000, Beijing Zhongshan Biotechnology Co., Ltd); ARID1A (1:300, CUSABIO TECHNOLOGY LLC); E‐cadherin Polyclonal antibody, cat on: 20874‐1‐AP; and Vimentin Polyclonal antibody, cat no: 10366‐1‐AP after blocking with 5% non‐fat milk in Tris‐buffered saline containing 0.05%Tween‐20 (1–1000).

Techniques: Knockdown, Expressing, Transfection

ARID1A silencing alters VIM and E‐cadherin expression (A and B) VIM and CDH1 expression were altered in WB results after ARID1A knocked down for 24 and 48 h.

Journal: Journal of Cellular and Molecular Medicine

Article Title: ARID1A downregulation promotes cell proliferation and migration of colon cancer via VIM activation and CDH1 suppression

doi: 10.1111/jcmm.17590

Figure Lengend Snippet: ARID1A silencing alters VIM and E‐cadherin expression (A and B) VIM and CDH1 expression were altered in WB results after ARID1A knocked down for 24 and 48 h.

Article Snippet: The membrane was incubated overnight at 4°C with rabbit antibodies against β‐actin (1:1000, Beijing Zhongshan Biotechnology Co., Ltd); ARID1A (1:300, CUSABIO TECHNOLOGY LLC); E‐cadherin Polyclonal antibody, cat on: 20874‐1‐AP; and Vimentin Polyclonal antibody, cat no: 10366‐1‐AP after blocking with 5% non‐fat milk in Tris‐buffered saline containing 0.05%Tween‐20 (1–1000).

Techniques: Expressing

ARID1A knockdown promotes colon cell line migration and proliferation (A and B) The effect of ARID1A depletion on HCT116 and LS174T cell migration (C) The effect of ARID1A depletion on LS174T cell invasion (D) The proliferation of HCT116 cells was assessed at specified times following ARID1A siRNA transfection (E) Immunoprecipitated DNA from ChIP experiments with anti‐ARID1A antibody was examined by real‐time qPCR using E‐cadherin and Vimentin‐specific promoter primers. IP stands for Immunoprecipitated. *p < 0.05, **p < 0.001, and ***p < 0.0001. Statistical differences were calculated using an imageJ software.

Journal: Journal of Cellular and Molecular Medicine

Article Title: ARID1A downregulation promotes cell proliferation and migration of colon cancer via VIM activation and CDH1 suppression

doi: 10.1111/jcmm.17590

Figure Lengend Snippet: ARID1A knockdown promotes colon cell line migration and proliferation (A and B) The effect of ARID1A depletion on HCT116 and LS174T cell migration (C) The effect of ARID1A depletion on LS174T cell invasion (D) The proliferation of HCT116 cells was assessed at specified times following ARID1A siRNA transfection (E) Immunoprecipitated DNA from ChIP experiments with anti‐ARID1A antibody was examined by real‐time qPCR using E‐cadherin and Vimentin‐specific promoter primers. IP stands for Immunoprecipitated. *p < 0.05, **p < 0.001, and ***p < 0.0001. Statistical differences were calculated using an imageJ software.

Article Snippet: The membrane was incubated overnight at 4°C with rabbit antibodies against β‐actin (1:1000, Beijing Zhongshan Biotechnology Co., Ltd); ARID1A (1:300, CUSABIO TECHNOLOGY LLC); E‐cadherin Polyclonal antibody, cat on: 20874‐1‐AP; and Vimentin Polyclonal antibody, cat no: 10366‐1‐AP after blocking with 5% non‐fat milk in Tris‐buffered saline containing 0.05%Tween‐20 (1–1000).

Techniques: Knockdown, Migration, Transfection, Immunoprecipitation, Software

List of 87  ARID1A  interaction proteins in HCT116

Journal: Journal of Cellular and Molecular Medicine

Article Title: ARID1A downregulation promotes cell proliferation and migration of colon cancer via VIM activation and CDH1 suppression

doi: 10.1111/jcmm.17590

Figure Lengend Snippet: List of 87 ARID1A interaction proteins in HCT116

Article Snippet: The membrane was incubated overnight at 4°C with rabbit antibodies against β‐actin (1:1000, Beijing Zhongshan Biotechnology Co., Ltd); ARID1A (1:300, CUSABIO TECHNOLOGY LLC); E‐cadherin Polyclonal antibody, cat on: 20874‐1‐AP; and Vimentin Polyclonal antibody, cat no: 10366‐1‐AP after blocking with 5% non‐fat milk in Tris‐buffered saline containing 0.05%Tween‐20 (1–1000).

Techniques:

Figure 1. Immunohistochemical staining for ARID1A. (A) Preserved expression; (B) Loss of expres- sion. Magnification: 200×.

Journal: Diagnostics (Basel, Switzerland)

Article Title: Relevance of ARID1A Mutations in Endometrial Carcinomas.

doi: 10.3390/diagnostics12030592

Figure Lengend Snippet: Figure 1. Immunohistochemical staining for ARID1A. (A) Preserved expression; (B) Loss of expres- sion. Magnification: 200×.

Article Snippet: ARID1A expression was evaluated using the rabbit anti-ARID1A polyclonal antibody (Atlas Antibodies AB, Sweden—1:90 dilution).

Techniques: Immunohistochemical staining, Staining, Expressing

Figure 2. ARID1A expression between wildtype and mutant patients by RNAseq. WT: ARID1A wildtype samples; MUT: ARID1A mutant samples.

Journal: Diagnostics (Basel, Switzerland)

Article Title: Relevance of ARID1A Mutations in Endometrial Carcinomas.

doi: 10.3390/diagnostics12030592

Figure Lengend Snippet: Figure 2. ARID1A expression between wildtype and mutant patients by RNAseq. WT: ARID1A wildtype samples; MUT: ARID1A mutant samples.

Article Snippet: ARID1A expression was evaluated using the rabbit anti-ARID1A polyclonal antibody (Atlas Antibodies AB, Sweden—1:90 dilution).

Techniques: Expressing, Mutagenesis

Figure 3. ARID1A expression between wildtype and mutant patients by qRT-PCR. WT: ARID1A wildtype samples; MUT: ARID1A mutant samples.

Journal: Diagnostics (Basel, Switzerland)

Article Title: Relevance of ARID1A Mutations in Endometrial Carcinomas.

doi: 10.3390/diagnostics12030592

Figure Lengend Snippet: Figure 3. ARID1A expression between wildtype and mutant patients by qRT-PCR. WT: ARID1A wildtype samples; MUT: ARID1A mutant samples.

Article Snippet: ARID1A expression was evaluated using the rabbit anti-ARID1A polyclonal antibody (Atlas Antibodies AB, Sweden—1:90 dilution).

Techniques: Expressing, Mutagenesis, Quantitative RT-PCR

Figure 4. Details of ARID1A Leu1100 (A), Asn1705 (B), Arg1833 (C), Arg1906 (D), and Leu2195 (E) and of the neighboring residues in the available structures. In each panel, the wildtype structure and the mutant calculated in silico have been reported on the left and on the right, respectively. ARID1A helices are in blue, while helices and strands from other SWI/SNF subunits are in light blue and in light yellow. The considered residue is in ball-and-stick representation while the residues in the vicinity are in sticks. The atoms are colored according to the atom type. The hydrogen bonds have been highlighted by using yellow dashed lines.

Journal: Diagnostics (Basel, Switzerland)

Article Title: Relevance of ARID1A Mutations in Endometrial Carcinomas.

doi: 10.3390/diagnostics12030592

Figure Lengend Snippet: Figure 4. Details of ARID1A Leu1100 (A), Asn1705 (B), Arg1833 (C), Arg1906 (D), and Leu2195 (E) and of the neighboring residues in the available structures. In each panel, the wildtype structure and the mutant calculated in silico have been reported on the left and on the right, respectively. ARID1A helices are in blue, while helices and strands from other SWI/SNF subunits are in light blue and in light yellow. The considered residue is in ball-and-stick representation while the residues in the vicinity are in sticks. The atoms are colored according to the atom type. The hydrogen bonds have been highlighted by using yellow dashed lines.

Article Snippet: ARID1A expression was evaluated using the rabbit anti-ARID1A polyclonal antibody (Atlas Antibodies AB, Sweden—1:90 dilution).

Techniques: Mutagenesis, In Silico, Residue