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mouse monoclonal antibody fn1  (Proteintech)


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    Proteintech mouse monoclonal antibody fn1
    Dot plot of PCA based on fibroblasts-specific ( A ) and endothelial cell-specific ( B ) gene markers to estimate their ability in distinguish the LNs subtypes ( n = 68). C Box plots illustrating the differences in COL1A1, α-SMA, <t>FN1,</t> CD31, and LYVE1 gene expression between LNs subtypes ( n = 50, 35, 31, 32, 11, and 14). Each data point represents an individual LN (biological replicates). Box plots represent the median (center line), 25th and 75th percentiles (bounds of the box), and minimum and maximum values (whiskers). The mIF staining and quantification reveal differential expression of α-SMA, FN1, COL1A1 ( n = 20 and 16) ( D ) and LYVE-1, CD31 ( n = 24 and 18) ( E ) between NLN_C1 and NLN_C4. Each data point represents an individual LN (biological replicates). Data are presented as mean values ± SD. The p value was calculated using a two-sided Student’s t test. Scale bars indicate 100 μm, 500 μm, and 1000 μm respectively. Source data are provided as a Source Data file. F Sirius Red staining results of differences in fibrosis levels between NLN_C1 and NLN_C4. Scale bars indicate 1000 μm. PC principal component, PCA principal component analysis, mIF multiplex immunofluorescence, SD standard deviation.
    Mouse Monoclonal Antibody Fn1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 954 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 96 stars, based on 954 article reviews
    mouse monoclonal antibody fn1 - by Bioz Stars, 2026-02
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    Images

    1) Product Images from "Lymph nodes molecular subtypes unravel lymph nodes heterogeneity and clinical implications in colorectal cancer"

    Article Title: Lymph nodes molecular subtypes unravel lymph nodes heterogeneity and clinical implications in colorectal cancer

    Journal: Nature Communications

    doi: 10.1038/s41467-025-63200-z

    Dot plot of PCA based on fibroblasts-specific ( A ) and endothelial cell-specific ( B ) gene markers to estimate their ability in distinguish the LNs subtypes ( n = 68). C Box plots illustrating the differences in COL1A1, α-SMA, FN1, CD31, and LYVE1 gene expression between LNs subtypes ( n = 50, 35, 31, 32, 11, and 14). Each data point represents an individual LN (biological replicates). Box plots represent the median (center line), 25th and 75th percentiles (bounds of the box), and minimum and maximum values (whiskers). The mIF staining and quantification reveal differential expression of α-SMA, FN1, COL1A1 ( n = 20 and 16) ( D ) and LYVE-1, CD31 ( n = 24 and 18) ( E ) between NLN_C1 and NLN_C4. Each data point represents an individual LN (biological replicates). Data are presented as mean values ± SD. The p value was calculated using a two-sided Student’s t test. Scale bars indicate 100 μm, 500 μm, and 1000 μm respectively. Source data are provided as a Source Data file. F Sirius Red staining results of differences in fibrosis levels between NLN_C1 and NLN_C4. Scale bars indicate 1000 μm. PC principal component, PCA principal component analysis, mIF multiplex immunofluorescence, SD standard deviation.
    Figure Legend Snippet: Dot plot of PCA based on fibroblasts-specific ( A ) and endothelial cell-specific ( B ) gene markers to estimate their ability in distinguish the LNs subtypes ( n = 68). C Box plots illustrating the differences in COL1A1, α-SMA, FN1, CD31, and LYVE1 gene expression between LNs subtypes ( n = 50, 35, 31, 32, 11, and 14). Each data point represents an individual LN (biological replicates). Box plots represent the median (center line), 25th and 75th percentiles (bounds of the box), and minimum and maximum values (whiskers). The mIF staining and quantification reveal differential expression of α-SMA, FN1, COL1A1 ( n = 20 and 16) ( D ) and LYVE-1, CD31 ( n = 24 and 18) ( E ) between NLN_C1 and NLN_C4. Each data point represents an individual LN (biological replicates). Data are presented as mean values ± SD. The p value was calculated using a two-sided Student’s t test. Scale bars indicate 100 μm, 500 μm, and 1000 μm respectively. Source data are provided as a Source Data file. F Sirius Red staining results of differences in fibrosis levels between NLN_C1 and NLN_C4. Scale bars indicate 1000 μm. PC principal component, PCA principal component analysis, mIF multiplex immunofluorescence, SD standard deviation.

    Techniques Used: Gene Expression, Staining, Quantitative Proteomics, Multiplex Assay, Immunofluorescence, Standard Deviation



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    mouse monoclonal antibody fn1  (Proteintech)
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    Proteintech mouse monoclonal antibody fn1
    Dot plot of PCA based on fibroblasts-specific ( A ) and endothelial cell-specific ( B ) gene markers to estimate their ability in distinguish the LNs subtypes ( n = 68). C Box plots illustrating the differences in COL1A1, α-SMA, <t>FN1,</t> CD31, and LYVE1 gene expression between LNs subtypes ( n = 50, 35, 31, 32, 11, and 14). Each data point represents an individual LN (biological replicates). Box plots represent the median (center line), 25th and 75th percentiles (bounds of the box), and minimum and maximum values (whiskers). The mIF staining and quantification reveal differential expression of α-SMA, FN1, COL1A1 ( n = 20 and 16) ( D ) and LYVE-1, CD31 ( n = 24 and 18) ( E ) between NLN_C1 and NLN_C4. Each data point represents an individual LN (biological replicates). Data are presented as mean values ± SD. The p value was calculated using a two-sided Student’s t test. Scale bars indicate 100 μm, 500 μm, and 1000 μm respectively. Source data are provided as a Source Data file. F Sirius Red staining results of differences in fibrosis levels between NLN_C1 and NLN_C4. Scale bars indicate 1000 μm. PC principal component, PCA principal component analysis, mIF multiplex immunofluorescence, SD standard deviation.
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    mouse monoclonal anti fn1 antibody  (Proteintech)
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    Dot plot of PCA based on fibroblasts-specific ( A ) and endothelial cell-specific ( B ) gene markers to estimate their ability in distinguish the LNs subtypes ( n = 68). C Box plots illustrating the differences in COL1A1, α-SMA, <t>FN1,</t> CD31, and LYVE1 gene expression between LNs subtypes ( n = 50, 35, 31, 32, 11, and 14). Each data point represents an individual LN (biological replicates). Box plots represent the median (center line), 25th and 75th percentiles (bounds of the box), and minimum and maximum values (whiskers). The mIF staining and quantification reveal differential expression of α-SMA, FN1, COL1A1 ( n = 20 and 16) ( D ) and LYVE-1, CD31 ( n = 24 and 18) ( E ) between NLN_C1 and NLN_C4. Each data point represents an individual LN (biological replicates). Data are presented as mean values ± SD. The p value was calculated using a two-sided Student’s t test. Scale bars indicate 100 μm, 500 μm, and 1000 μm respectively. Source data are provided as a Source Data file. F Sirius Red staining results of differences in fibrosis levels between NLN_C1 and NLN_C4. Scale bars indicate 1000 μm. PC principal component, PCA principal component analysis, mIF multiplex immunofluorescence, SD standard deviation.
    Mouse Monoclonal Anti Fn1 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    mouse monoclonal anti-fn1 antibody  (Proteintech)
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    Dot plot of PCA based on fibroblasts-specific ( A ) and endothelial cell-specific ( B ) gene markers to estimate their ability in distinguish the LNs subtypes ( n = 68). C Box plots illustrating the differences in COL1A1, α-SMA, <t>FN1,</t> CD31, and LYVE1 gene expression between LNs subtypes ( n = 50, 35, 31, 32, 11, and 14). Each data point represents an individual LN (biological replicates). Box plots represent the median (center line), 25th and 75th percentiles (bounds of the box), and minimum and maximum values (whiskers). The mIF staining and quantification reveal differential expression of α-SMA, FN1, COL1A1 ( n = 20 and 16) ( D ) and LYVE-1, CD31 ( n = 24 and 18) ( E ) between NLN_C1 and NLN_C4. Each data point represents an individual LN (biological replicates). Data are presented as mean values ± SD. The p value was calculated using a two-sided Student’s t test. Scale bars indicate 100 μm, 500 μm, and 1000 μm respectively. Source data are provided as a Source Data file. F Sirius Red staining results of differences in fibrosis levels between NLN_C1 and NLN_C4. Scale bars indicate 1000 μm. PC principal component, PCA principal component analysis, mIF multiplex immunofluorescence, SD standard deviation.
    Mouse Monoclonal Anti Fn1 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Dot plot of PCA based on fibroblasts-specific ( A ) and endothelial cell-specific ( B ) gene markers to estimate their ability in distinguish the LNs subtypes ( n = 68). C Box plots illustrating the differences in COL1A1, α-SMA, <t>FN1,</t> CD31, and LYVE1 gene expression between LNs subtypes ( n = 50, 35, 31, 32, 11, and 14). Each data point represents an individual LN (biological replicates). Box plots represent the median (center line), 25th and 75th percentiles (bounds of the box), and minimum and maximum values (whiskers). The mIF staining and quantification reveal differential expression of α-SMA, FN1, COL1A1 ( n = 20 and 16) ( D ) and LYVE-1, CD31 ( n = 24 and 18) ( E ) between NLN_C1 and NLN_C4. Each data point represents an individual LN (biological replicates). Data are presented as mean values ± SD. The p value was calculated using a two-sided Student’s t test. Scale bars indicate 100 μm, 500 μm, and 1000 μm respectively. Source data are provided as a Source Data file. F Sirius Red staining results of differences in fibrosis levels between NLN_C1 and NLN_C4. Scale bars indicate 1000 μm. PC principal component, PCA principal component analysis, mIF multiplex immunofluorescence, SD standard deviation.
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    mouse monoclonal primary antibodies against fn1  (Santa Cruz Biotechnology)
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    Immunostaining of cells for <t>CDH1</t> (A) and FN1 (B) proteins. (i) HEY cells (not transfected), HEY cells transfected with (ii) nc-miR, (iii) miR-200a, (iv) miR-141, (v) miR-200b, (vi) miR-200c, and (vii) miR-429. DAPI was used to stain the cell nuclei. Scale bars, 50 μm.
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    anti fibronectin mouse mab ma1116  (Boster Bio)
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    Immunostaining of cells for <t>CDH1</t> (A) and FN1 (B) proteins. (i) HEY cells (not transfected), HEY cells transfected with (ii) nc-miR, (iii) miR-200a, (iv) miR-141, (v) miR-200b, (vi) miR-200c, and (vii) miR-429. DAPI was used to stain the cell nuclei. Scale bars, 50 μm.
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    Log2 fold change in <t>FN1</t> gene expression in GC tissues. (A) FN1 expression in tumor tissues compared with that in normal tissues. (B) FN1 expression in the advanced T stage (T2 + T3 + T4) group compared with that in the early T stage (T1) group. (C) FN1 expression in the low differentiation group (high tumor grade) compared with that in the high differentiation group (intermediate and low tumor grade). (D) FN1 expression in the high clinical TNM stage (III+IV) group compared with that in the low clinical TNM stage (I+II) group. Error bars represent 95% confidence interval. *P<0.05 and **P<0.01 vs. normal tissue. FN1 , fibronectin 1; TNM, Tumor-Node-Metastasis; ns, non-significant.
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    fibronectin (fn1) mouse monoclonal antibody  (OriGene)
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    Log2 fold change in <t>FN1</t> gene expression in GC tissues. (A) FN1 expression in tumor tissues compared with that in normal tissues. (B) FN1 expression in the advanced T stage (T2 + T3 + T4) group compared with that in the early T stage (T1) group. (C) FN1 expression in the low differentiation group (high tumor grade) compared with that in the high differentiation group (intermediate and low tumor grade). (D) FN1 expression in the high clinical TNM stage (III+IV) group compared with that in the low clinical TNM stage (I+II) group. Error bars represent 95% confidence interval. *P<0.05 and **P<0.01 vs. normal tissue. FN1 , fibronectin 1; TNM, Tumor-Node-Metastasis; ns, non-significant.
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    Image Search Results


    Dot plot of PCA based on fibroblasts-specific ( A ) and endothelial cell-specific ( B ) gene markers to estimate their ability in distinguish the LNs subtypes ( n = 68). C Box plots illustrating the differences in COL1A1, α-SMA, FN1, CD31, and LYVE1 gene expression between LNs subtypes ( n = 50, 35, 31, 32, 11, and 14). Each data point represents an individual LN (biological replicates). Box plots represent the median (center line), 25th and 75th percentiles (bounds of the box), and minimum and maximum values (whiskers). The mIF staining and quantification reveal differential expression of α-SMA, FN1, COL1A1 ( n = 20 and 16) ( D ) and LYVE-1, CD31 ( n = 24 and 18) ( E ) between NLN_C1 and NLN_C4. Each data point represents an individual LN (biological replicates). Data are presented as mean values ± SD. The p value was calculated using a two-sided Student’s t test. Scale bars indicate 100 μm, 500 μm, and 1000 μm respectively. Source data are provided as a Source Data file. F Sirius Red staining results of differences in fibrosis levels between NLN_C1 and NLN_C4. Scale bars indicate 1000 μm. PC principal component, PCA principal component analysis, mIF multiplex immunofluorescence, SD standard deviation.

    Journal: Nature Communications

    Article Title: Lymph nodes molecular subtypes unravel lymph nodes heterogeneity and clinical implications in colorectal cancer

    doi: 10.1038/s41467-025-63200-z

    Figure Lengend Snippet: Dot plot of PCA based on fibroblasts-specific ( A ) and endothelial cell-specific ( B ) gene markers to estimate their ability in distinguish the LNs subtypes ( n = 68). C Box plots illustrating the differences in COL1A1, α-SMA, FN1, CD31, and LYVE1 gene expression between LNs subtypes ( n = 50, 35, 31, 32, 11, and 14). Each data point represents an individual LN (biological replicates). Box plots represent the median (center line), 25th and 75th percentiles (bounds of the box), and minimum and maximum values (whiskers). The mIF staining and quantification reveal differential expression of α-SMA, FN1, COL1A1 ( n = 20 and 16) ( D ) and LYVE-1, CD31 ( n = 24 and 18) ( E ) between NLN_C1 and NLN_C4. Each data point represents an individual LN (biological replicates). Data are presented as mean values ± SD. The p value was calculated using a two-sided Student’s t test. Scale bars indicate 100 μm, 500 μm, and 1000 μm respectively. Source data are provided as a Source Data file. F Sirius Red staining results of differences in fibrosis levels between NLN_C1 and NLN_C4. Scale bars indicate 1000 μm. PC principal component, PCA principal component analysis, mIF multiplex immunofluorescence, SD standard deviation.

    Article Snippet: The primary antibodies included rabbit polyclonal antibody CXCL13/BCA1 (Proteintech, 10927-1-AP); rabbit polyclonal antibody LYVE1 (Proteintech, 28321-1-AP); mouse monoclonal antibody CD20 (Proteintech, 60271-1-Ig); mouse monoclonal antibody FN1 (Proteintech, 66042-1-Ig); mouse monoclonal antibody CD31 (Proteintech, 66065-2-Ig); mouse monoclonal antibody COL1A1 (Proteintech, 67288-1-Ig); mouse monoclonal antibody PDPN (Proteintech, 67432-1-Ig); mouse monoclonal antibody CD35 (Proteintech, 68033-1-Ig); rabbit recombinant antibody α-SMA (Proteintech, 80008-1-RR); All images were captured using an EVOS FL Auto 2 Imaging System (Thermo Fisher Scientific).

    Techniques: Gene Expression, Staining, Quantitative Proteomics, Multiplex Assay, Immunofluorescence, Standard Deviation

    Immunostaining of cells for CDH1 (A) and FN1 (B) proteins. (i) HEY cells (not transfected), HEY cells transfected with (ii) nc-miR, (iii) miR-200a, (iv) miR-141, (v) miR-200b, (vi) miR-200c, and (vii) miR-429. DAPI was used to stain the cell nuclei. Scale bars, 50 μm.

    Journal: Journal of Ovarian Research

    Article Title: Sequence variation among members of the miR-200 microRNA family is correlated with variation in the ability to induce hallmarks of mesenchymal-epithelial transition in ovarian cancer cells

    doi: 10.1186/1757-2215-7-12

    Figure Lengend Snippet: Immunostaining of cells for CDH1 (A) and FN1 (B) proteins. (i) HEY cells (not transfected), HEY cells transfected with (ii) nc-miR, (iii) miR-200a, (iv) miR-141, (v) miR-200b, (vi) miR-200c, and (vii) miR-429. DAPI was used to stain the cell nuclei. Scale bars, 50 μm.

    Article Snippet: The slides were incubated with mouse monoclonal primary antibodies against CDH1 (E-cadherin) and FN1 (Fibronectin, 1:200; Santa Cruz Biotechnology, Inc., Santa Cruz, CA) in 5% BSA for 1 hour at room temperature.

    Techniques: Immunostaining, Transfection, Staining

    Log2 fold change in FN1 gene expression in GC tissues. (A) FN1 expression in tumor tissues compared with that in normal tissues. (B) FN1 expression in the advanced T stage (T2 + T3 + T4) group compared with that in the early T stage (T1) group. (C) FN1 expression in the low differentiation group (high tumor grade) compared with that in the high differentiation group (intermediate and low tumor grade). (D) FN1 expression in the high clinical TNM stage (III+IV) group compared with that in the low clinical TNM stage (I+II) group. Error bars represent 95% confidence interval. *P<0.05 and **P<0.01 vs. normal tissue. FN1 , fibronectin 1; TNM, Tumor-Node-Metastasis; ns, non-significant.

    Journal: Oncology Letters

    Article Title: High expression of fibronectin 1 indicates poor prognosis in gastric cancer

    doi: 10.3892/ol.2019.11088

    Figure Lengend Snippet: Log2 fold change in FN1 gene expression in GC tissues. (A) FN1 expression in tumor tissues compared with that in normal tissues. (B) FN1 expression in the advanced T stage (T2 + T3 + T4) group compared with that in the early T stage (T1) group. (C) FN1 expression in the low differentiation group (high tumor grade) compared with that in the high differentiation group (intermediate and low tumor grade). (D) FN1 expression in the high clinical TNM stage (III+IV) group compared with that in the low clinical TNM stage (I+II) group. Error bars represent 95% confidence interval. *P<0.05 and **P<0.01 vs. normal tissue. FN1 , fibronectin 1; TNM, Tumor-Node-Metastasis; ns, non-significant.

    Article Snippet: A mouse monoclonal antibody against FN1 (cat. no. 66042-1-Ig; ProteinTech Group, Inc.) was used at a 1:600 dilution at pH 9.0.

    Techniques: Gene Expression, Expressing

    Forest plot and meta-analysis of FN1 expression in gastric cancer. (A) Forest plot of the log2 fold change in FN1 expression in tumor tissues compared with that in normal tissues. (B) Forest plot of the log2 fold change in FN1 expression in the advanced T stage group (T2 + T3 + T4) compared with that in the early T stage group (T1). (C) Forest plot of the log2 fold change in FN1 expression in the low differentiation group (high tumor grade) compared with that in the high differentiation group (intermediate and low tumor grade). (D) Forest plot of the log2 fold change in FN1 expression in the high clinical TNM stage (III+IV) group compared with that in the low clinical TNM stage (I+II) group. (E) Forest plot of the comparison of overall survival in patients with gastric cancer with high and low FN1 expression (The gene expression value was equal to three, the first two-thirds were defined as high expression and the last one-third as low expression). FN1 , fibronectin 1; TNM, Tumor-Node-Metastasis; CI, confidence interval.

    Journal: Oncology Letters

    Article Title: High expression of fibronectin 1 indicates poor prognosis in gastric cancer

    doi: 10.3892/ol.2019.11088

    Figure Lengend Snippet: Forest plot and meta-analysis of FN1 expression in gastric cancer. (A) Forest plot of the log2 fold change in FN1 expression in tumor tissues compared with that in normal tissues. (B) Forest plot of the log2 fold change in FN1 expression in the advanced T stage group (T2 + T3 + T4) compared with that in the early T stage group (T1). (C) Forest plot of the log2 fold change in FN1 expression in the low differentiation group (high tumor grade) compared with that in the high differentiation group (intermediate and low tumor grade). (D) Forest plot of the log2 fold change in FN1 expression in the high clinical TNM stage (III+IV) group compared with that in the low clinical TNM stage (I+II) group. (E) Forest plot of the comparison of overall survival in patients with gastric cancer with high and low FN1 expression (The gene expression value was equal to three, the first two-thirds were defined as high expression and the last one-third as low expression). FN1 , fibronectin 1; TNM, Tumor-Node-Metastasis; CI, confidence interval.

    Article Snippet: A mouse monoclonal antibody against FN1 (cat. no. 66042-1-Ig; ProteinTech Group, Inc.) was used at a 1:600 dilution at pH 9.0.

    Techniques: Expressing, Comparison, Gene Expression

    Kaplan-Meier survival curves of the high- and low- FN1 expression groups in six cohorts. Survival curves for the following datasets: (A) GSE14208; (B) GSE15459; (C) GSE29272; (D) GSE34942; (E) GSE66229 and (F) TCGA. FN1 , fibronectin 1; TCGA, The Cancer Genome Atlas.

    Journal: Oncology Letters

    Article Title: High expression of fibronectin 1 indicates poor prognosis in gastric cancer

    doi: 10.3892/ol.2019.11088

    Figure Lengend Snippet: Kaplan-Meier survival curves of the high- and low- FN1 expression groups in six cohorts. Survival curves for the following datasets: (A) GSE14208; (B) GSE15459; (C) GSE29272; (D) GSE34942; (E) GSE66229 and (F) TCGA. FN1 , fibronectin 1; TCGA, The Cancer Genome Atlas.

    Article Snippet: A mouse monoclonal antibody against FN1 (cat. no. 66042-1-Ig; ProteinTech Group, Inc.) was used at a 1:600 dilution at pH 9.0.

    Techniques: Expressing

    Immunohistochemical analysis of FN1 in GC. (A) Normal gastric mucosa exhibited negative staining for FN1 . (B-D) E- FN1 expression in GS tissues. (B) Expression score, 0; (C) expression score, 6; and (D) expression score, 12. (E-H) S- FN1 expression in in GS tissues. (E) No expression; (F) low expression; (G) medium expression; and (H) high expression. Magnification, ×200. GC, gastric cancer; FN1 , fibronectin 1; S- FN1 , stromal FN1 ; E- FN1 , epithelial FN1 .

    Journal: Oncology Letters

    Article Title: High expression of fibronectin 1 indicates poor prognosis in gastric cancer

    doi: 10.3892/ol.2019.11088

    Figure Lengend Snippet: Immunohistochemical analysis of FN1 in GC. (A) Normal gastric mucosa exhibited negative staining for FN1 . (B-D) E- FN1 expression in GS tissues. (B) Expression score, 0; (C) expression score, 6; and (D) expression score, 12. (E-H) S- FN1 expression in in GS tissues. (E) No expression; (F) low expression; (G) medium expression; and (H) high expression. Magnification, ×200. GC, gastric cancer; FN1 , fibronectin 1; S- FN1 , stromal FN1 ; E- FN1 , epithelial FN1 .

    Article Snippet: A mouse monoclonal antibody against FN1 (cat. no. 66042-1-Ig; ProteinTech Group, Inc.) was used at a 1:600 dilution at pH 9.0.

    Techniques: Immunohistochemical staining, Negative Staining, Expressing

    Patient characteristics based on the immunohistochemistry results of FN1 expression in gastric cancer.

    Journal: Oncology Letters

    Article Title: High expression of fibronectin 1 indicates poor prognosis in gastric cancer

    doi: 10.3892/ol.2019.11088

    Figure Lengend Snippet: Patient characteristics based on the immunohistochemistry results of FN1 expression in gastric cancer.

    Article Snippet: A mouse monoclonal antibody against FN1 (cat. no. 66042-1-Ig; ProteinTech Group, Inc.) was used at a 1:600 dilution at pH 9.0.

    Techniques: Immunohistochemistry, Expressing

    Association between epithelial and stromal expression of FN1 in gastric cancer.

    Journal: Oncology Letters

    Article Title: High expression of fibronectin 1 indicates poor prognosis in gastric cancer

    doi: 10.3892/ol.2019.11088

    Figure Lengend Snippet: Association between epithelial and stromal expression of FN1 in gastric cancer.

    Article Snippet: A mouse monoclonal antibody against FN1 (cat. no. 66042-1-Ig; ProteinTech Group, Inc.) was used at a 1:600 dilution at pH 9.0.

    Techniques: Expressing

    The prognostic significance of FN1 in patients with gastric cancer based on immunohistochemistry. (A) Kaplan-Meier analysis of OS based on E- FN1 expression in 190 patients. (B) Kaplan-Meier analysis of OS based on S- FN1 expression in 190 patients. (C and D) Kaplan-Meier analysis of OS based on S- FN1 expression in patients with (C) TNM stage I+II (D) and III+IV gastric cancer. FN1 , fibronectin 1; S- FN1 , stromal FN1 ; E- FN1 , epithelial FN1 ; TNM, Tumor-Node-Metastasis; OS, overall survival.

    Journal: Oncology Letters

    Article Title: High expression of fibronectin 1 indicates poor prognosis in gastric cancer

    doi: 10.3892/ol.2019.11088

    Figure Lengend Snippet: The prognostic significance of FN1 in patients with gastric cancer based on immunohistochemistry. (A) Kaplan-Meier analysis of OS based on E- FN1 expression in 190 patients. (B) Kaplan-Meier analysis of OS based on S- FN1 expression in 190 patients. (C and D) Kaplan-Meier analysis of OS based on S- FN1 expression in patients with (C) TNM stage I+II (D) and III+IV gastric cancer. FN1 , fibronectin 1; S- FN1 , stromal FN1 ; E- FN1 , epithelial FN1 ; TNM, Tumor-Node-Metastasis; OS, overall survival.

    Article Snippet: A mouse monoclonal antibody against FN1 (cat. no. 66042-1-Ig; ProteinTech Group, Inc.) was used at a 1:600 dilution at pH 9.0.

    Techniques: Immunohistochemistry, Expressing

    Multivariate analysis of overall survival in 190 patients with gastric cancer.

    Journal: Oncology Letters

    Article Title: High expression of fibronectin 1 indicates poor prognosis in gastric cancer

    doi: 10.3892/ol.2019.11088

    Figure Lengend Snippet: Multivariate analysis of overall survival in 190 patients with gastric cancer.

    Article Snippet: A mouse monoclonal antibody against FN1 (cat. no. 66042-1-Ig; ProteinTech Group, Inc.) was used at a 1:600 dilution at pH 9.0.

    Techniques: Expressing