anti vimentin Search Results


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Developmental Studies Hybridoma Bank vimentin
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R&D Systems antibody production recombinant human vimentin rhvim
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Santa Cruz Biotechnology vimentin
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
Vimentin, supplied by Santa Cruz Biotechnology, 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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Cell Signaling Technology Inc anti phospho vimentin ser56
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
Anti Phospho Vimentin Ser56, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Valiant Co Ltd monoclonal mouse antibody
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
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Proteintech vimentin
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
Vimentin, 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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Cell Signaling Technology Inc antitwist
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
Antitwist, supplied by Cell Signaling Technology Inc, 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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Bioss vimentin
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
Vimentin, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sino Biological vimentin
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
Vimentin, supplied by Sino Biological, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems vimentin
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
Vimentin, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluidigm standard biotools 3143027d
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
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Boster Bio antibodies mouse anti human monoclonal antibody
Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization <t>of</t> <t>E-cadherin</t> (green) and <t>vimentin</t> (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.
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Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization of E-cadherin (green) and vimentin (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.

Journal: Cancer cell

Article Title: Loss of p53 in enterocytes generates an inflammatory microenvironment enabling invasion and lymph node metastasis of carcinogen-induced colorectal tumors.

doi: 10.1016/j.ccr.2012.11.014

Figure Lengend Snippet: Figure 4. Activation of NF-kB Is Associated with Cxcl1 and Twist Upregulation in p53-Deficient Invasive Carcinoma (A) GSEA comparing all differentially regulated genes from AOM-induced invasive cancers in Tp53DIEC mice with a data set of NF-kB target genes obtained from microdissected invading human tumor epithelia (Horst et al., 2009). Normalized enrichment score: 1.46; p < 0.0001. (B) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (C–F) Immunohistochemical analysis of activated p-p65 (C), CXCL1 (D), F4/80 (E), and Gr-1 (F) in invasive cancers of AOM-challenged Tp53DIEC mice. Dashed white lines mark the basal membrane. Scale bars represent 50 mm. (G) Immunoblot analysis for the indicated proteins in lysates from invasive cancers from Tp53DIEC mice and noninvasive adenomas from Tp53F/F mice 16 weeks after the first AOM administration. (H) Immunohistochemical analysis of Twist in invasive cancers of AOM-challenged Tp53DIEC mice. The scale bar represents 50 mm. (I) Colocalization of E-cadherin (green) and vimentin (red) in invasive cancer epithelial cells of AOM-challenged Tp53DIEC mice, indicating EMT; nuclei are stained using 40,6-diamidino-2-phenylindole (blue). The scale bar represents 200 mm. (J–M) Representative immunohistochemical analysis of p53 (J and L) and p-p65 (K and M) in human colon cancer samples. Scale bars represent 100 mm. (N) Correlation of p53 staining and p-p65 staining (n = 59; c2 test, p < 0.05). (O) Correlation of p-p65 staining and the presence of lymph node (LN) metastases (n = 59; c2 test, p < 0.02). (P) Relative CD68 mRNA level in human colon cancer patients who were characterized by expression of both p53 and p-p65 (p53+/p-p65+; n = 23) or not (other; n = 30). Data are mean ± SE; *p < 0.05 by t test. (Q and R) Representative immunohistochemical staining of CD68 in human colon cancer patients who were characterized by expression of both p53 and phospho-p65 (Q) or the absence of p53 and phospho-p65 (R). Scale bars represent 100 mm. See also Figure S3.

Article Snippet: Standard immunohistochemical procedures were performed using the following antibodies: b-catenin (Santa Cruz; sc-1496), bromodeoxyuridine (BrdU) (AbD Serotec; MCA 2060), cleaved caspase-3 (Cell Signaling; 9661), CXCL1 (R&DSystems;MAB453), F4/80 (Caltag; MF48000), Gr-1 (eBioscience; 12-5931-82), phospho-Histone H2A.X (Cell Signaling; 2577), E-cadherin (Becton Dickinson; 610182), Twist (Abcam; 49254), vimentin (Santa Cruz; SC-7557), VE-cadherin (Santa Cruz; SC-6458), and occludin (Invitrogen; 711500).

Techniques: Activation Assay, Western Blot, Immunohistochemical staining, Membrane, Staining, Expressing