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cdh1  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc cdh1
    Cdh1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 5529 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti-cdh1/E-Cadherin+Rabbit+mAb/pm41904140-251-32-44
    Average 98 stars, based on 5529 article reviews
    cdh1 - by Bioz Stars, 2026-09
    98/100 stars

    Images

    Related Articles

    Immunofluorescence:

    Article Title: Classification of Atretic Small Antral Follicles in the Human Ovary
    Article Snippet: The primary antibodies used were mouse anti-CYP19A1 (1:100, sc-374176, Santa Cruz, Dallas, TX, USA), mouse anti-AR (1:100, sc-7305, Santa Cruz), mouse anti-AMH (1:100, MCA2246T, BioRad, Hercules, CA, USA), rabbit anti-CDH1 (1:100, CST3195S, Cell Signaling, Danvers, MA, USA), rabbit anti-MKI67 (1:100, ab15580, Abcam, Cambridge, UK), rabbit anti-cCASP3 (Asp175) (1:100, CST9661S, Cell Signaling), rabbit anti-COLLIV (1:100, AB748, Merck), mouse anti-CD68 (1:100, M087629-2, DAKO, Glostrup, Denmark), rabbit anti-ACTA2 (1:100, ab5694, Abcam), mouse anti-STAR (D-2) (1:100, sc-166821, Santa Cruz), rabbit anti-GSTA1 (1:100, HPA053817, Atlas Antibodies, Bromma, Sweden).


    Staining:

    Article Title: Classification of Atretic Small Antral Follicles in the Human Ovary
    Article Snippet: The primary antibodies used were mouse anti-CYP19A1 (1:100, sc-374176, Santa Cruz, Dallas, TX, USA), mouse anti-AR (1:100, sc-7305, Santa Cruz), mouse anti-AMH (1:100, MCA2246T, BioRad, Hercules, CA, USA), rabbit anti-CDH1 (1:100, CST3195S, Cell Signaling, Danvers, MA, USA), rabbit anti-MKI67 (1:100, ab15580, Abcam, Cambridge, UK), rabbit anti-cCASP3 (Asp175) (1:100, CST9661S, Cell Signaling), rabbit anti-COLLIV (1:100, AB748, Merck), mouse anti-CD68 (1:100, M087629-2, DAKO, Glostrup, Denmark), rabbit anti-ACTA2 (1:100, ab5694, Abcam), mouse anti-STAR (D-2) (1:100, sc-166821, Santa Cruz), rabbit anti-GSTA1 (1:100, HPA053817, Atlas Antibodies, Bromma, Sweden).


    Expressing:

    Article Title: Classification of Atretic Small Antral Follicles in the Human Ovary
    Article Snippet: The primary antibodies used were mouse anti-CYP19A1 (1:100, sc-374176, Santa Cruz, Dallas, TX, USA), mouse anti-AR (1:100, sc-7305, Santa Cruz), mouse anti-AMH (1:100, MCA2246T, BioRad, Hercules, CA, USA), rabbit anti-CDH1 (1:100, CST3195S, Cell Signaling, Danvers, MA, USA), rabbit anti-MKI67 (1:100, ab15580, Abcam, Cambridge, UK), rabbit anti-cCASP3 (Asp175) (1:100, CST9661S, Cell Signaling), rabbit anti-COLLIV (1:100, AB748, Merck), mouse anti-CD68 (1:100, M087629-2, DAKO, Glostrup, Denmark), rabbit anti-ACTA2 (1:100, ab5694, Abcam), mouse anti-STAR (D-2) (1:100, sc-166821, Santa Cruz), rabbit anti-GSTA1 (1:100, HPA053817, Atlas Antibodies, Bromma, Sweden).


    TUNEL Assay:

    Article Title: Classification of Atretic Small Antral Follicles in the Human Ovary
    Article Snippet: The primary antibodies used were mouse anti-CYP19A1 (1:100, sc-374176, Santa Cruz, Dallas, TX, USA), mouse anti-AR (1:100, sc-7305, Santa Cruz), mouse anti-AMH (1:100, MCA2246T, BioRad, Hercules, CA, USA), rabbit anti-CDH1 (1:100, CST3195S, Cell Signaling, Danvers, MA, USA), rabbit anti-MKI67 (1:100, ab15580, Abcam, Cambridge, UK), rabbit anti-cCASP3 (Asp175) (1:100, CST9661S, Cell Signaling), rabbit anti-COLLIV (1:100, AB748, Merck), mouse anti-CD68 (1:100, M087629-2, DAKO, Glostrup, Denmark), rabbit anti-ACTA2 (1:100, ab5694, Abcam), mouse anti-STAR (D-2) (1:100, sc-166821, Santa Cruz), rabbit anti-GSTA1 (1:100, HPA053817, Atlas Antibodies, Bromma, Sweden).




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    The number of lipid droplets in bEECs is related to the cell morphology: ( A ) The representative images of lipid droplets and cytoskeleton staining in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. BODIPY 493/503, F-action and DAPI marked lipid droplets, cytoskeleton and cell nuclei, respectively. Scale bar: 50 μm. ( B ) The fluorescence intensity analysis of BODIPY 493/503 staining in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. ( C ) The analysis of PLIN2 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. ( D , E ) The representative images and analysis of PLIN2 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( F , G ) The representative images and analysis of ZO-1 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( H , I ) The representative images and analysis of <t>CDH1</t> expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( J , K ) The representative images and analysis of β-catenin expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. The data are means ± SEM of three independent experiments. Statistically significant differences are indicated by asterisks: * p < 0.05, ** p < 0.01, ns p > 0.05.
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    The number of lipid droplets in bEECs is related to the cell morphology: ( A ) The representative images of lipid droplets and cytoskeleton staining in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. BODIPY 493/503, F-action and DAPI marked lipid droplets, cytoskeleton and cell nuclei, respectively. Scale bar: 50 μm. ( B ) The fluorescence intensity analysis of BODIPY 493/503 staining in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. ( C ) The analysis of PLIN2 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. ( D , E ) The representative images and analysis of PLIN2 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( F , G ) The representative images and analysis of ZO-1 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( H , I ) The representative images and analysis of <t>CDH1</t> expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( J , K ) The representative images and analysis of β-catenin expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. The data are means ± SEM of three independent experiments. Statistically significant differences are indicated by asterisks: * p < 0.05, ** p < 0.01, ns p > 0.05.
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    Image Search Results


    The number of lipid droplets in bEECs is related to the cell morphology: ( A ) The representative images of lipid droplets and cytoskeleton staining in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. BODIPY 493/503, F-action and DAPI marked lipid droplets, cytoskeleton and cell nuclei, respectively. Scale bar: 50 μm. ( B ) The fluorescence intensity analysis of BODIPY 493/503 staining in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. ( C ) The analysis of PLIN2 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. ( D , E ) The representative images and analysis of PLIN2 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( F , G ) The representative images and analysis of ZO-1 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( H , I ) The representative images and analysis of CDH1 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( J , K ) The representative images and analysis of β-catenin expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. The data are means ± SEM of three independent experiments. Statistically significant differences are indicated by asterisks: * p < 0.05, ** p < 0.01, ns p > 0.05.

    Journal: Animals : an Open Access Journal from MDPI

    Article Title: FABP3 Mediates Lipid Droplet Accumulation and Adhesive Capacity in Bovine Endometrial Epithelial Cells via PGE 2 /PTGER4/PPAR Axis

    doi: 10.3390/ani15233417

    Figure Lengend Snippet: The number of lipid droplets in bEECs is related to the cell morphology: ( A ) The representative images of lipid droplets and cytoskeleton staining in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. BODIPY 493/503, F-action and DAPI marked lipid droplets, cytoskeleton and cell nuclei, respectively. Scale bar: 50 μm. ( B ) The fluorescence intensity analysis of BODIPY 493/503 staining in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. ( C ) The analysis of PLIN2 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA. ( D , E ) The representative images and analysis of PLIN2 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( F , G ) The representative images and analysis of ZO-1 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( H , I ) The representative images and analysis of CDH1 expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. ( J , K ) The representative images and analysis of β-catenin expression in bEECs after treatment with 5% FBS, 1% BSA or 5% FBS + OA, respectively. The data are means ± SEM of three independent experiments. Statistically significant differences are indicated by asterisks: * p < 0.05, ** p < 0.01, ns p > 0.05.

    Article Snippet: After blocking with 5% non-fat milk for 2 h, the membranes were incubated with primary antibodies at 4 °C overnight, including anti-PLIN2 antibody (1:1000, ab181452, Abcam) [ ], anti-CDH1 antibody (1:1000, 3195, Cell Signaling Technology, Danvers, MA, USA) [ ], anti-ZO-1 antibody (1:1000, 21773-1-AP, Proteintech, bovine), anti-β-catenin antibody (1:500, sc-53484, Santa Cruz, CA, USA) [ ], anti-FABP3 antibody (1:1000, ab133585, Abcam), anti-OPN antibody (1:1000, 22952-1-AP, Proteintech) [ ], anti-ITGB3 antibody (1:1000, CY5237, Abways, Shanghai, China), anti-PTGER2 antibody (1:1000, ab167171, Abcam), anti-PTGER4 antibody (1:1000, ab217966, Abcam), anti-β-Tubulin antibody (1:2000, 56739S, Cell signaling Technology) [ ] and anti-GAPDH (1:2000, 60004-1-Ig, Proteintech) [ ].

    Techniques: Staining, Fluorescence, Expressing

    The expression of FABP3 regulates endometrial epithelial cell remodeling: ( A , B ) The representative images and analysis of BTCs spheroid adhesion rate in bEECs after FABP3 knockdown, respectively. BTCs: Bovine placental trophoblast cells. Scale bar: 200 μm. ( C ) Representative images of scanning electron microscope in the microvilli structure on the surface of bEECs after FABP3 knockdown. Scale bar: 20 μm (Others), 10 μm (Enlarge). ( D – F ) The representative images and analysis of the protein expression related to cell adhesion (OPN and ITGB3) in bEECs between shN and shFABP3 groups, respectively. ( G – J ) The representative images and analysis of the protein expression (ZO-1, CDH1 and β-catenin) in bEECs between shN and shFABP3 groups, respectively. The data are means ± SEM of three independent experiments. Statistically significant differences are indicated by asterisks: * p < 0.05, ** p < 0.01, ns p > 0.05.

    Journal: Animals : an Open Access Journal from MDPI

    Article Title: FABP3 Mediates Lipid Droplet Accumulation and Adhesive Capacity in Bovine Endometrial Epithelial Cells via PGE 2 /PTGER4/PPAR Axis

    doi: 10.3390/ani15233417

    Figure Lengend Snippet: The expression of FABP3 regulates endometrial epithelial cell remodeling: ( A , B ) The representative images and analysis of BTCs spheroid adhesion rate in bEECs after FABP3 knockdown, respectively. BTCs: Bovine placental trophoblast cells. Scale bar: 200 μm. ( C ) Representative images of scanning electron microscope in the microvilli structure on the surface of bEECs after FABP3 knockdown. Scale bar: 20 μm (Others), 10 μm (Enlarge). ( D – F ) The representative images and analysis of the protein expression related to cell adhesion (OPN and ITGB3) in bEECs between shN and shFABP3 groups, respectively. ( G – J ) The representative images and analysis of the protein expression (ZO-1, CDH1 and β-catenin) in bEECs between shN and shFABP3 groups, respectively. The data are means ± SEM of three independent experiments. Statistically significant differences are indicated by asterisks: * p < 0.05, ** p < 0.01, ns p > 0.05.

    Article Snippet: After blocking with 5% non-fat milk for 2 h, the membranes were incubated with primary antibodies at 4 °C overnight, including anti-PLIN2 antibody (1:1000, ab181452, Abcam) [ ], anti-CDH1 antibody (1:1000, 3195, Cell Signaling Technology, Danvers, MA, USA) [ ], anti-ZO-1 antibody (1:1000, 21773-1-AP, Proteintech, bovine), anti-β-catenin antibody (1:500, sc-53484, Santa Cruz, CA, USA) [ ], anti-FABP3 antibody (1:1000, ab133585, Abcam), anti-OPN antibody (1:1000, 22952-1-AP, Proteintech) [ ], anti-ITGB3 antibody (1:1000, CY5237, Abways, Shanghai, China), anti-PTGER2 antibody (1:1000, ab167171, Abcam), anti-PTGER4 antibody (1:1000, ab217966, Abcam), anti-β-Tubulin antibody (1:2000, 56739S, Cell signaling Technology) [ ] and anti-GAPDH (1:2000, 60004-1-Ig, Proteintech) [ ].

    Techniques: Expressing, Knockdown, Microscopy

    Expression of E-cadherin in resectable gastric cancer tissues (magnification, ×200). (A) E-cadherin-positive group. (B) E-cadherin-negative group.

    Journal: Oncology Letters

    Article Title: Clinical importance of E-cadherin deficiency in resectable gastric cancer: A nested case-control study

    doi: 10.3892/ol.2025.15173

    Figure Lengend Snippet: Expression of E-cadherin in resectable gastric cancer tissues (magnification, ×200). (A) E-cadherin-positive group. (B) E-cadherin-negative group.

    Article Snippet: Rabbit anti-human E-cadherin antibody (clone number, EP6; Beijing Zhongshan Jinqiao Biotechnology Co., Ltd.) was utilized for immunohistochemical staining.

    Techniques: Expressing

    Comparison of curves of DFS between patients with E-cadherin deficiency and E-cadherin-positive expression in resectable gastric cancer after propensity score matching (P=0.590). DFS, disease-free survival.

    Journal: Oncology Letters

    Article Title: Clinical importance of E-cadherin deficiency in resectable gastric cancer: A nested case-control study

    doi: 10.3892/ol.2025.15173

    Figure Lengend Snippet: Comparison of curves of DFS between patients with E-cadherin deficiency and E-cadherin-positive expression in resectable gastric cancer after propensity score matching (P=0.590). DFS, disease-free survival.

    Article Snippet: Rabbit anti-human E-cadherin antibody (clone number, EP6; Beijing Zhongshan Jinqiao Biotechnology Co., Ltd.) was utilized for immunohistochemical staining.

    Techniques: Comparison, Expressing

    Comparison of curves of OS between patients with E-cadherin deficiency and E-cadherin-positive expression in resectable gastric cancer after propensity score matching (P=0.863). OS, overall survival.

    Journal: Oncology Letters

    Article Title: Clinical importance of E-cadherin deficiency in resectable gastric cancer: A nested case-control study

    doi: 10.3892/ol.2025.15173

    Figure Lengend Snippet: Comparison of curves of OS between patients with E-cadherin deficiency and E-cadherin-positive expression in resectable gastric cancer after propensity score matching (P=0.863). OS, overall survival.

    Article Snippet: Rabbit anti-human E-cadherin antibody (clone number, EP6; Beijing Zhongshan Jinqiao Biotechnology Co., Ltd.) was utilized for immunohistochemical staining.

    Techniques: Comparison, Expressing