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e cadherin  (Proteintech)


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    Structured Review

    Proteintech e cadherin
    circSMAD4 drives tumor-educated M2-like polarization of macrophages and promotes tumor-cell aggressiveness. (A) Workflow for generating TC-hMDMs and TC-BMDMs, circSMAD4 knockdown, and downstream functional assays. (B) RT–qPCR analysis of M1-associated markers (MHC-II [HLA-DRA in TC-hMDMs; H2-Ab1 in TC-BMDMs], NOS2, and CD86) and M2-associated markers (CD163, CD206, and ARG1) in TC-hMDMs and TC-BMDMs. (C) Representative flow-cytometry histograms for HLA-DR, iNOS, CD86, CD163, CD206, and ARG1 in TC-hMDMs. Gating strategy and marker thresholds were defined based on FMO controls (see ). (D) Flow-cytometry quantification of marker-positive cells in TC-hMDMs and TC-BMDMs. (E) ELISA of IL-10, TGF-β, and iNOS in culture supernatants. (F) CCK-8 assays of A549 and LLC cells. (G) Colony-formation assays of A549 and LLC cells with quantification. (H) Bioluminescence-based growth readouts of patient-derived LUAD organoids (PDO #1 and PDO #2) after co-culture with TC-hMDMs. (I) Immunoblot analysis of EMT-related proteins <t>(E-cadherin,</t> N-cadherin, Vimentin) in A549 and LLC cells. (J) Transwell migration and invasion assays of A549 and LLC cells with quantification. Scale bar, 50 μm. ∗P < 0.05; ∗∗P < 0.01; ∗∗∗P < 0.001; ∗∗∗∗P < 0.0001; ns, not significant.
    E Cadherin, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 3363 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/polyclonal/E-cadherin+Polyclonal+antibody/pmc13050104-89-12-13
    Average 96 stars, based on 3363 article reviews
    e cadherin - by Bioz Stars, 2026-11
    96/100 stars

    Images

    1) Product Images from "CircSMAD4 shapes matrix-remodeling TAMs in lung adenocarcinoma"

    Article Title: CircSMAD4 shapes matrix-remodeling TAMs in lung adenocarcinoma

    Journal: Non-coding RNA Research

    doi: 10.1016/j.ncrna.2026.03.003

    circSMAD4 drives tumor-educated M2-like polarization of macrophages and promotes tumor-cell aggressiveness. (A) Workflow for generating TC-hMDMs and TC-BMDMs, circSMAD4 knockdown, and downstream functional assays. (B) RT–qPCR analysis of M1-associated markers (MHC-II [HLA-DRA in TC-hMDMs; H2-Ab1 in TC-BMDMs], NOS2, and CD86) and M2-associated markers (CD163, CD206, and ARG1) in TC-hMDMs and TC-BMDMs. (C) Representative flow-cytometry histograms for HLA-DR, iNOS, CD86, CD163, CD206, and ARG1 in TC-hMDMs. Gating strategy and marker thresholds were defined based on FMO controls (see ). (D) Flow-cytometry quantification of marker-positive cells in TC-hMDMs and TC-BMDMs. (E) ELISA of IL-10, TGF-β, and iNOS in culture supernatants. (F) CCK-8 assays of A549 and LLC cells. (G) Colony-formation assays of A549 and LLC cells with quantification. (H) Bioluminescence-based growth readouts of patient-derived LUAD organoids (PDO #1 and PDO #2) after co-culture with TC-hMDMs. (I) Immunoblot analysis of EMT-related proteins (E-cadherin, N-cadherin, Vimentin) in A549 and LLC cells. (J) Transwell migration and invasion assays of A549 and LLC cells with quantification. Scale bar, 50 μm. ∗P < 0.05; ∗∗P < 0.01; ∗∗∗P < 0.001; ∗∗∗∗P < 0.0001; ns, not significant.
    Figure Legend Snippet: circSMAD4 drives tumor-educated M2-like polarization of macrophages and promotes tumor-cell aggressiveness. (A) Workflow for generating TC-hMDMs and TC-BMDMs, circSMAD4 knockdown, and downstream functional assays. (B) RT–qPCR analysis of M1-associated markers (MHC-II [HLA-DRA in TC-hMDMs; H2-Ab1 in TC-BMDMs], NOS2, and CD86) and M2-associated markers (CD163, CD206, and ARG1) in TC-hMDMs and TC-BMDMs. (C) Representative flow-cytometry histograms for HLA-DR, iNOS, CD86, CD163, CD206, and ARG1 in TC-hMDMs. Gating strategy and marker thresholds were defined based on FMO controls (see ). (D) Flow-cytometry quantification of marker-positive cells in TC-hMDMs and TC-BMDMs. (E) ELISA of IL-10, TGF-β, and iNOS in culture supernatants. (F) CCK-8 assays of A549 and LLC cells. (G) Colony-formation assays of A549 and LLC cells with quantification. (H) Bioluminescence-based growth readouts of patient-derived LUAD organoids (PDO #1 and PDO #2) after co-culture with TC-hMDMs. (I) Immunoblot analysis of EMT-related proteins (E-cadherin, N-cadherin, Vimentin) in A549 and LLC cells. (J) Transwell migration and invasion assays of A549 and LLC cells with quantification. Scale bar, 50 μm. ∗P < 0.05; ∗∗P < 0.01; ∗∗∗P < 0.001; ∗∗∗∗P < 0.0001; ns, not significant.

    Techniques Used: Knockdown, Functional Assay, Quantitative RT-PCR, Flow Cytometry, Marker, Enzyme-linked Immunosorbent Assay, CCK-8 Assay, Derivative Assay, Co-Culture Assay, Western Blot, Migration

    circSMAD4 depletion in macrophages restrains LUAD growth and metastasis in vivo. (A) Schematic of orthotopic lung implantation and experimental metastasis models using LLC cells mixed with BMDMs expressing shNC or sh-circSMAD4. (B) Representative images of orthotopic lung tumors. (C) Tumor weight of orthotopic implants. (D) Overall survival of mice bearing orthotopic tumors. (E) Immunofluorescence showing F4/80 and circSMAD4 signals in tumor tissues. Scale bar, 50 μm. (F, G) Representative Ki-67 IHC staining and quantification in orthotopic tumors. Scale bar, 50 μm. (H) Representative bioluminescence images of lung tumor burden in the metastasis model. (I) Tumor weight in the metastasis model. (J) Overall survival of mice in the metastasis model. (K–M) Representative IHC staining and quantification of E-cadherin and vimentin in tumors. Scale bar, 50 μm. ∗P < 0.05; ∗∗P < 0.01; ∗∗∗P < 0.001; ∗∗∗∗P < 0.0001; ns, not significant.
    Figure Legend Snippet: circSMAD4 depletion in macrophages restrains LUAD growth and metastasis in vivo. (A) Schematic of orthotopic lung implantation and experimental metastasis models using LLC cells mixed with BMDMs expressing shNC or sh-circSMAD4. (B) Representative images of orthotopic lung tumors. (C) Tumor weight of orthotopic implants. (D) Overall survival of mice bearing orthotopic tumors. (E) Immunofluorescence showing F4/80 and circSMAD4 signals in tumor tissues. Scale bar, 50 μm. (F, G) Representative Ki-67 IHC staining and quantification in orthotopic tumors. Scale bar, 50 μm. (H) Representative bioluminescence images of lung tumor burden in the metastasis model. (I) Tumor weight in the metastasis model. (J) Overall survival of mice in the metastasis model. (K–M) Representative IHC staining and quantification of E-cadherin and vimentin in tumors. Scale bar, 50 μm. ∗P < 0.05; ∗∗P < 0.01; ∗∗∗P < 0.001; ∗∗∗∗P < 0.0001; ns, not significant.

    Techniques Used: In Vivo, Expressing, Immunofluorescence, Immunohistochemistry

    Related Articles

    Western Blot:

    Article Title: Curcumin analogue FLLL32 induces ferroptosis by targeting the STAT3-GPX4/SLC40A1 axis in colorectal cancer
    Article Snippet: .. Primary antibodies used for immunoblot analysis were as follows: β-Tubulin (ZSGB-BIO, TA347064), STAT3 (HUABIO, ET1603-40), Phospho-STAT3 (Tyr705) (CST, 9145S), GPX4 (HUABIO, ET1706-45), SLC40A1 (CST, 80672T), FTH1 (Abclonal, A1144), FTL (Abclonal, A1768), Lamin B1 (Abclonal, A11495), E-cadherin (Proteintech, 20874-1-AP), N-cadherin (Proteintech, 22018-1-AP), Vimentin (Proteintech, 10366-1-AP), and HA-tag (Proteintech, 66006-2-Ig). .. HRP-conjugated goat anti-rabbit IgG (ZSGB-BIO, ZF-0511) and HRP-conjugated goat anti-mouse IgG (ZSGB-BIO, ZB-5305) were used as secondary antibodies.

    Article Title: Mitochondrial modulator M1 attenuates ovarian aging by remodeling granulosa cell metabolism and improving oocyte maturation.
    Article Snippet: Ovarian aging is characterized by granulosa cell (GC) dysfunction and compromised oocyte maturation, yet effective mitochondria-targeted interventions remain limited.. We investigated the association of the mitochondrial fusion promoter M1 with age-related transcriptional, mitochondrial, and metabolic phenotypes.. Reanalysis of public single-cell transcriptomic data identified ageassociated differences in a granulosa-enriched cluster across mitochondrial dynamics-related, glycolysis/lactate metabolic, bioenergetic/TCA-cycle, and granulosa-cell phenotype programs.

    Analysis:

    Article Title: Curcumin analogue FLLL32 induces ferroptosis by targeting the STAT3-GPX4/SLC40A1 axis in colorectal cancer
    Article Snippet: .. Primary antibodies used for immunoblot analysis were as follows: β-Tubulin (ZSGB-BIO, TA347064), STAT3 (HUABIO, ET1603-40), Phospho-STAT3 (Tyr705) (CST, 9145S), GPX4 (HUABIO, ET1706-45), SLC40A1 (CST, 80672T), FTH1 (Abclonal, A1144), FTL (Abclonal, A1768), Lamin B1 (Abclonal, A11495), E-cadherin (Proteintech, 20874-1-AP), N-cadherin (Proteintech, 22018-1-AP), Vimentin (Proteintech, 10366-1-AP), and HA-tag (Proteintech, 66006-2-Ig). .. HRP-conjugated goat anti-rabbit IgG (ZSGB-BIO, ZF-0511) and HRP-conjugated goat anti-mouse IgG (ZSGB-BIO, ZB-5305) were used as secondary antibodies.

    Hemagglutination Assay:

    Article Title: Curcumin analogue FLLL32 induces ferroptosis by targeting the STAT3-GPX4/SLC40A1 axis in colorectal cancer
    Article Snippet: .. Primary antibodies used for immunoblot analysis were as follows: β-Tubulin (ZSGB-BIO, TA347064), STAT3 (HUABIO, ET1603-40), Phospho-STAT3 (Tyr705) (CST, 9145S), GPX4 (HUABIO, ET1706-45), SLC40A1 (CST, 80672T), FTH1 (Abclonal, A1144), FTL (Abclonal, A1768), Lamin B1 (Abclonal, A11495), E-cadherin (Proteintech, 20874-1-AP), N-cadherin (Proteintech, 22018-1-AP), Vimentin (Proteintech, 10366-1-AP), and HA-tag (Proteintech, 66006-2-Ig). .. HRP-conjugated goat anti-rabbit IgG (ZSGB-BIO, ZF-0511) and HRP-conjugated goat anti-mouse IgG (ZSGB-BIO, ZB-5305) were used as secondary antibodies.

    Incubation:

    Article Title: ZDHHC5-mediated S-palmitoylation of NOD2 drives neutrophil extracellular trap formation via mitophagy to exacerbate inflammation in COPD
    Article Snippet: .. Subsequently, slices were subjected to overnight incubation at 4 °C with primary antibodies against NOD2 (Cat. #30628-1-AP, Proteintech, Wuhan, China), ZDHHC5 (Cat. #21324-1-AP, Proteintech), E-cadherin (Cat. #20874-1-AP, Proteintech), or N-cadherin (Cat. # AF4039, Affinity Bioscience, Changzhou, China). .. Slices were rinsed in phosphate-buffered saline (PBS), followed by 1-h incubation at RT with an HRP-labeled goat anti-rabbit secondary antibody (Cat. #ab6721, Abcam).

    Article Title: Carrier-Free Cur/DTX@ICG Ternary Nanoparticles for Suppressing Lung Metastasis in Triple-Negative Breast Cancer.
    Article Snippet: Chemotherapy for advanced breast cancer may promote metastatic progression through inflammatory responses.. To address this challenge, we developed carrier-free Cur/DTX@ICG nanoparticles via molecular co-assembly, achieving a high drugloading capacity of 66.7%.. This theranostic platform integrates docetaxel, curcumin, and indocyanine green for chemotherapy, anti-inflammatory chemosensitization, and fluorescence imaging.

    Article Title: Chronic co-exposure to benzo[a]pyrene and BDE-47 induces malignant transformation of human mammary epithelial cells via dysregulation of the miR-491-5p/VPS28 axis.
    Article Snippet: Benzo[a]pyrene (B[a]P) and 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) are widespread environmental pollutants associated with breast carcinogenesis, yet their combined effects remain unclear.. In this study, a chronic low-dose exposure model was established using human mammary epithelial MCF-10A cells to investigate coexposure-induced malignant transformation and underlying mechanisms.. Both single and combined exposures promoted proliferation, clonogenicity, epithelial–mesenchymal transition, and tumorigenicity.

    Cell-Signaling:

    Article Title: Mitochondrial modulator M1 attenuates ovarian aging by remodeling granulosa cell metabolism and improving oocyte maturation.
    Article Snippet: Ovarian aging is characterized by granulosa cell (GC) dysfunction and compromised oocyte maturation, yet effective mitochondria-targeted interventions remain limited.. We investigated the association of the mitochondrial fusion promoter M1 with age-related transcriptional, mitochondrial, and metabolic phenotypes.. Reanalysis of public single-cell transcriptomic data identified ageassociated differences in a granulosa-enriched cluster across mitochondrial dynamics-related, glycolysis/lactate metabolic, bioenergetic/TCA-cycle, and granulosa-cell phenotype programs.

    Membrane:

    Article Title: Chronic co-exposure to benzo[a]pyrene and BDE-47 induces malignant transformation of human mammary epithelial cells via dysregulation of the miR-491-5p/VPS28 axis.
    Article Snippet: Benzo[a]pyrene (B[a]P) and 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) are widespread environmental pollutants associated with breast carcinogenesis, yet their combined effects remain unclear.. In this study, a chronic low-dose exposure model was established using human mammary epithelial MCF-10A cells to investigate coexposure-induced malignant transformation and underlying mechanisms.. Both single and combined exposures promoted proliferation, clonogenicity, epithelial–mesenchymal transition, and tumorigenicity.



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