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p smad2  (Bioss)


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    Structured Review

    Bioss p smad2
    LPS induced activation of rat uterine fibroblasts. (A) WB detection of LAMC2 expression levels in epithelial cells, (B) Relative expression of LAMC2 in epithelial cells, (C) Level of LAMC2 in cells detected by ELISA in epithelial cells, (D) WB detection of E-cad, N-cad, α-SMA,TGF-β1, <t>SMAD2/3</t> in fibroblasts, (E) Relative expression of E-cad, N-cad, α-SMA,TGF-β1, SMAD2, SMAD3 in fibroblasts, (F) Immunofluorescence staining of COL1A1 in fibroblasts, (G) Immunofluorescence staining of COL3A1 in fibroblasts, (H) Immunofluorescence staining of α-SMA in fibroblasts, (I) Mean fluorescence intensity of COL1A1, COL3A1 and α-SMA. Compared to model in fibroblasts, * P < 0.05, ** P < 0.01.
    P Smad2, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/p+smad2/Smad2(Ser465+%2B+Ser467)+Antibody/pmc13106170-115-52-56
    Average 94 stars, based on 19 article reviews
    p smad2 - by Bioz Stars, 2026-09
    94/100 stars

    Images

    1) Product Images from "Molecular mechanism of Danshen injection in treating endometrial fibrosis induced by intrauterine adhesions via the LAMC2-CD44-TGF-β1-SMAD2/3 signaling pathway"

    Article Title: Molecular mechanism of Danshen injection in treating endometrial fibrosis induced by intrauterine adhesions via the LAMC2-CD44-TGF-β1-SMAD2/3 signaling pathway

    Journal: Frontiers in Physiology

    doi: 10.3389/fphys.2026.1794215

    LPS induced activation of rat uterine fibroblasts. (A) WB detection of LAMC2 expression levels in epithelial cells, (B) Relative expression of LAMC2 in epithelial cells, (C) Level of LAMC2 in cells detected by ELISA in epithelial cells, (D) WB detection of E-cad, N-cad, α-SMA,TGF-β1, SMAD2/3 in fibroblasts, (E) Relative expression of E-cad, N-cad, α-SMA,TGF-β1, SMAD2, SMAD3 in fibroblasts, (F) Immunofluorescence staining of COL1A1 in fibroblasts, (G) Immunofluorescence staining of COL3A1 in fibroblasts, (H) Immunofluorescence staining of α-SMA in fibroblasts, (I) Mean fluorescence intensity of COL1A1, COL3A1 and α-SMA. Compared to model in fibroblasts, * P < 0.05, ** P < 0.01.
    Figure Legend Snippet: LPS induced activation of rat uterine fibroblasts. (A) WB detection of LAMC2 expression levels in epithelial cells, (B) Relative expression of LAMC2 in epithelial cells, (C) Level of LAMC2 in cells detected by ELISA in epithelial cells, (D) WB detection of E-cad, N-cad, α-SMA,TGF-β1, SMAD2/3 in fibroblasts, (E) Relative expression of E-cad, N-cad, α-SMA,TGF-β1, SMAD2, SMAD3 in fibroblasts, (F) Immunofluorescence staining of COL1A1 in fibroblasts, (G) Immunofluorescence staining of COL3A1 in fibroblasts, (H) Immunofluorescence staining of α-SMA in fibroblasts, (I) Mean fluorescence intensity of COL1A1, COL3A1 and α-SMA. Compared to model in fibroblasts, * P < 0.05, ** P < 0.01.

    Techniques Used: Activation Assay, Expressing, Enzyme-linked Immunosorbent Assay, Immunofluorescence, Staining, Fluorescence

    Danshen injection improves endometrial fibrosis in IUA rats by inhibiting the LAMC2-CD44-TGF-β1- SMAD2/3 signaling pathway. (A) Uterine Weight, (B) Uterine Length, (C) Grading of intrauterine adhesions in each group, (D) Number of uterine glands, (E) Collagen volume fraction, (F) H&E Staining, (G) MASSON Staining, (H) Immunofluorescence staining of COL1A1, (I) Immunofluorescence staining of COL3A1, (J) Immunofluorescence staining of α-SMA, (K) Mean fluorescence intensity of COL1A1, COL3A1 and α-SMA, L: WB detection of LAMC2, TGF-β1, SMAD2, SMAD3, (L) Relative expression of protein LAMC2, TGF-β1, SMAD2, SMAD3. Compared to model, * P < 0.05, ** P < 0.01. For panels A-C, n = 6 independent animals per group; for panels (D–M) , n=3 independent animals per group.
    Figure Legend Snippet: Danshen injection improves endometrial fibrosis in IUA rats by inhibiting the LAMC2-CD44-TGF-β1- SMAD2/3 signaling pathway. (A) Uterine Weight, (B) Uterine Length, (C) Grading of intrauterine adhesions in each group, (D) Number of uterine glands, (E) Collagen volume fraction, (F) H&E Staining, (G) MASSON Staining, (H) Immunofluorescence staining of COL1A1, (I) Immunofluorescence staining of COL3A1, (J) Immunofluorescence staining of α-SMA, (K) Mean fluorescence intensity of COL1A1, COL3A1 and α-SMA, L: WB detection of LAMC2, TGF-β1, SMAD2, SMAD3, (L) Relative expression of protein LAMC2, TGF-β1, SMAD2, SMAD3. Compared to model, * P < 0.05, ** P < 0.01. For panels A-C, n = 6 independent animals per group; for panels (D–M) , n=3 independent animals per group.

    Techniques Used: Injection, Staining, Immunofluorescence, Fluorescence, Expressing

    Related Articles

    other:


    Membrane:

    Article Title: Mechanistic Insights into Yunpi-Xiefei-Huatan decoction effects on autophagy and MUC5AC secretion in rat tracheal epithelial cells via the TGF-β3/Smad2/Smad3 pathway.
    Article Snippet: Ethnopharmacological relevance: Bronchial asthma (BA) is a common chronic respiratory disease in children.. Yunpi–Xiefei–Huatan decoction (YXHD) is known to relieve cough and reduce phlegm, and is widely applied in the clinical treatment of childhood asthma.. However, its mechanism of action has not been fully elucidated.

    Blocking Assay:

    Article Title: Mechanistic Insights into Yunpi-Xiefei-Huatan decoction effects on autophagy and MUC5AC secretion in rat tracheal epithelial cells via the TGF-β3/Smad2/Smad3 pathway.
    Article Snippet: Ethnopharmacological relevance: Bronchial asthma (BA) is a common chronic respiratory disease in children.. Yunpi–Xiefei–Huatan decoction (YXHD) is known to relieve cough and reduce phlegm, and is widely applied in the clinical treatment of childhood asthma.. However, its mechanism of action has not been fully elucidated.

    Incubation:

    Article Title: Mechanistic Insights into Yunpi-Xiefei-Huatan decoction effects on autophagy and MUC5AC secretion in rat tracheal epithelial cells via the TGF-β3/Smad2/Smad3 pathway.
    Article Snippet: Ethnopharmacological relevance: Bronchial asthma (BA) is a common chronic respiratory disease in children.. Yunpi–Xiefei–Huatan decoction (YXHD) is known to relieve cough and reduce phlegm, and is widely applied in the clinical treatment of childhood asthma.. However, its mechanism of action has not been fully elucidated.

    Article Title: Regulation of Smad2/3 Nuclear Exclusion by Follicle-Stimulating Hormone (FSH) in Chicken Follicular Granulosa Cells and Its Effect on FOXO3/4
    Article Snippet: The protein concentration was adjusted using a BCA assay kit (Beyotime, Shanghai, China), following the manufacturer’s instructions. .. Protein samples were separated using 10% SDS-PAGE gel (Epizyme Biotech, Shanghai, China), and the proteins were transferred to membranes after electrophoresis at 150 V. The membranes were blocked with 5% skim milk powder and incubated overnight at 4 °C with the following primary antibodies: anti-FOXO3 (Proteintech, Wuhan, China, 1:2000 dilution), p-FOXO3 (Bioss, Beijing, China, 1:1000 dilution), anti-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), p-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad2 (Bioss, Beijing, China, 1:1000 dilution), p-Smad2 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad3 (Bioss, Beijing, China, 1:1000 dilution), p-Smad3 (Bioss, Beijing, China, 1:1000 dilution), and anti-β-actin (Boster Biological Technology, Wuhan, China, 1:10,000 dilution). ..

    Article Title: Regulation of Smad2/3 Nuclear Exclusion by Follicle-Stimulating Hormone (FSH) in Chicken Follicular Granulosa Cells and Its Effect on FOXO3/4
    Article Snippet: The protein concentration was adjusted using a BCA assay kit (Beyotime, Shanghai, China), following the manufacturer’s instructions. .. Protein samples were separated using 10% SDS-PAGE gel (Epizyme Biotech, Shanghai, China), and the proteins were transferred to membranes after electrophoresis at 150 V. The membranes were blocked with 5% skim milk powder and incubated overnight at 4 ◦C with the following primary antibodies: anti-FOXO3 (Proteintech, Wuhan, China, 1:2000 dilution), p-FOXO3 (Bioss, Beijing, China, 1:1000 dilution), anti-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), p-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad2 (Bioss, Beijing, China, 1:1000 dilution), p-Smad2 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad3 (Bioss, Beijing, China, 1:1000 dilution), p-Smad3 (Bioss, Beijing, China, 1:1000 dilution), and anti-β-actin (Boster Biological Technology, Wuhan, China, 1:10,000 dilution). ..

    Article Title: The mutualistic relationship between M2c macrophages of TGFβ1 induction and gastric cancer cells: the correlation between protective mechanisms in the tumor microenvironment and polarization of subtypes of cells
    Article Snippet: .. After 2 h of closure with skimmed milk in TBST, the membranes were analyzed using TNF-α (Boster, A00002-5), IL-10 (Boster, A00021-2), TGFβ1 (Boster, BM4876), Smad2 (Immunoway, YP1185), p-Smad2 (Bioss, bs-20341R), Smad3 (Immunoway, YT4334), p-Smad3 (Bioss, bs-5235R), E-cadherin (Immunoway, YM0207), N-cadherin (Immunoway, YM4937), Vimentin (Immunoway, YT4880), GAPDH (Boster, BA2913), GPX4 (Boster, BM5231), FSP1 (Proteintech, #20886-1-AP), DHODH (Boster, M04035-1) and SLC7A11 (Boster, BM5318) were incubated overnight at 4°C. ..

    SDS Page:

    Article Title: Regulation of Smad2/3 Nuclear Exclusion by Follicle-Stimulating Hormone (FSH) in Chicken Follicular Granulosa Cells and Its Effect on FOXO3/4
    Article Snippet: The protein concentration was adjusted using a BCA assay kit (Beyotime, Shanghai, China), following the manufacturer’s instructions. .. Protein samples were separated using 10% SDS-PAGE gel (Epizyme Biotech, Shanghai, China), and the proteins were transferred to membranes after electrophoresis at 150 V. The membranes were blocked with 5% skim milk powder and incubated overnight at 4 °C with the following primary antibodies: anti-FOXO3 (Proteintech, Wuhan, China, 1:2000 dilution), p-FOXO3 (Bioss, Beijing, China, 1:1000 dilution), anti-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), p-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad2 (Bioss, Beijing, China, 1:1000 dilution), p-Smad2 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad3 (Bioss, Beijing, China, 1:1000 dilution), p-Smad3 (Bioss, Beijing, China, 1:1000 dilution), and anti-β-actin (Boster Biological Technology, Wuhan, China, 1:10,000 dilution). ..

    Article Title: Regulation of Smad2/3 Nuclear Exclusion by Follicle-Stimulating Hormone (FSH) in Chicken Follicular Granulosa Cells and Its Effect on FOXO3/4
    Article Snippet: The protein concentration was adjusted using a BCA assay kit (Beyotime, Shanghai, China), following the manufacturer’s instructions. .. Protein samples were separated using 10% SDS-PAGE gel (Epizyme Biotech, Shanghai, China), and the proteins were transferred to membranes after electrophoresis at 150 V. The membranes were blocked with 5% skim milk powder and incubated overnight at 4 ◦C with the following primary antibodies: anti-FOXO3 (Proteintech, Wuhan, China, 1:2000 dilution), p-FOXO3 (Bioss, Beijing, China, 1:1000 dilution), anti-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), p-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad2 (Bioss, Beijing, China, 1:1000 dilution), p-Smad2 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad3 (Bioss, Beijing, China, 1:1000 dilution), p-Smad3 (Bioss, Beijing, China, 1:1000 dilution), and anti-β-actin (Boster Biological Technology, Wuhan, China, 1:10,000 dilution). ..

    Electrophoresis:

    Article Title: Regulation of Smad2/3 Nuclear Exclusion by Follicle-Stimulating Hormone (FSH) in Chicken Follicular Granulosa Cells and Its Effect on FOXO3/4
    Article Snippet: The protein concentration was adjusted using a BCA assay kit (Beyotime, Shanghai, China), following the manufacturer’s instructions. .. Protein samples were separated using 10% SDS-PAGE gel (Epizyme Biotech, Shanghai, China), and the proteins were transferred to membranes after electrophoresis at 150 V. The membranes were blocked with 5% skim milk powder and incubated overnight at 4 °C with the following primary antibodies: anti-FOXO3 (Proteintech, Wuhan, China, 1:2000 dilution), p-FOXO3 (Bioss, Beijing, China, 1:1000 dilution), anti-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), p-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad2 (Bioss, Beijing, China, 1:1000 dilution), p-Smad2 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad3 (Bioss, Beijing, China, 1:1000 dilution), p-Smad3 (Bioss, Beijing, China, 1:1000 dilution), and anti-β-actin (Boster Biological Technology, Wuhan, China, 1:10,000 dilution). ..

    Article Title: Regulation of Smad2/3 Nuclear Exclusion by Follicle-Stimulating Hormone (FSH) in Chicken Follicular Granulosa Cells and Its Effect on FOXO3/4
    Article Snippet: The protein concentration was adjusted using a BCA assay kit (Beyotime, Shanghai, China), following the manufacturer’s instructions. .. Protein samples were separated using 10% SDS-PAGE gel (Epizyme Biotech, Shanghai, China), and the proteins were transferred to membranes after electrophoresis at 150 V. The membranes were blocked with 5% skim milk powder and incubated overnight at 4 ◦C with the following primary antibodies: anti-FOXO3 (Proteintech, Wuhan, China, 1:2000 dilution), p-FOXO3 (Bioss, Beijing, China, 1:1000 dilution), anti-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), p-FOXO4 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad2 (Bioss, Beijing, China, 1:1000 dilution), p-Smad2 (Bioss, Beijing, China, 1:1000 dilution), anti-Smad3 (Bioss, Beijing, China, 1:1000 dilution), p-Smad3 (Bioss, Beijing, China, 1:1000 dilution), and anti-β-actin (Boster Biological Technology, Wuhan, China, 1:10,000 dilution). ..



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    Image Search Results


    LPS induced activation of rat uterine fibroblasts. (A) WB detection of LAMC2 expression levels in epithelial cells, (B) Relative expression of LAMC2 in epithelial cells, (C) Level of LAMC2 in cells detected by ELISA in epithelial cells, (D) WB detection of E-cad, N-cad, α-SMA,TGF-β1, SMAD2/3 in fibroblasts, (E) Relative expression of E-cad, N-cad, α-SMA,TGF-β1, SMAD2, SMAD3 in fibroblasts, (F) Immunofluorescence staining of COL1A1 in fibroblasts, (G) Immunofluorescence staining of COL3A1 in fibroblasts, (H) Immunofluorescence staining of α-SMA in fibroblasts, (I) Mean fluorescence intensity of COL1A1, COL3A1 and α-SMA. Compared to model in fibroblasts, * P < 0.05, ** P < 0.01.

    Journal: Frontiers in Physiology

    Article Title: Molecular mechanism of Danshen injection in treating endometrial fibrosis induced by intrauterine adhesions via the LAMC2-CD44-TGF-β1-SMAD2/3 signaling pathway

    doi: 10.3389/fphys.2026.1794215

    Figure Lengend Snippet: LPS induced activation of rat uterine fibroblasts. (A) WB detection of LAMC2 expression levels in epithelial cells, (B) Relative expression of LAMC2 in epithelial cells, (C) Level of LAMC2 in cells detected by ELISA in epithelial cells, (D) WB detection of E-cad, N-cad, α-SMA,TGF-β1, SMAD2/3 in fibroblasts, (E) Relative expression of E-cad, N-cad, α-SMA,TGF-β1, SMAD2, SMAD3 in fibroblasts, (F) Immunofluorescence staining of COL1A1 in fibroblasts, (G) Immunofluorescence staining of COL3A1 in fibroblasts, (H) Immunofluorescence staining of α-SMA in fibroblasts, (I) Mean fluorescence intensity of COL1A1, COL3A1 and α-SMA. Compared to model in fibroblasts, * P < 0.05, ** P < 0.01.

    Article Snippet: Primary antibodies: CK-19 (1:1000; YM8269, Immunoway, USA), Vimentin (1:1000; YM8324, Immunoway, USA), GAPDH (1:1000; A19056, ABclonal, China), LAMC2 (1:1000; A1869, ABclonal, China), E-cad (1:1000; A20798, ABclonal, China), N-cad (1:500; A0433, ABclonal, China), α-SMA (1:1000; A2319, ABclonal, China), TGF-β1 (1:2000; A15103, ABclonal, China), SMAD2 (1:5000; bsm-52223R, Bioss, China), SMAD3 (1:1000; A16913, ABclonal, China), p- SMAD2 (1:5000; bs-3419R, Bioss, China), p- SMAD3 (1:2000; Ap0727, ABclonal, China), and a secondary antibody (1:2000; AS014, ABclonal, China).

    Techniques: Activation Assay, Expressing, Enzyme-linked Immunosorbent Assay, Immunofluorescence, Staining, Fluorescence

    Danshen injection improves endometrial fibrosis in IUA rats by inhibiting the LAMC2-CD44-TGF-β1- SMAD2/3 signaling pathway. (A) Uterine Weight, (B) Uterine Length, (C) Grading of intrauterine adhesions in each group, (D) Number of uterine glands, (E) Collagen volume fraction, (F) H&E Staining, (G) MASSON Staining, (H) Immunofluorescence staining of COL1A1, (I) Immunofluorescence staining of COL3A1, (J) Immunofluorescence staining of α-SMA, (K) Mean fluorescence intensity of COL1A1, COL3A1 and α-SMA, L: WB detection of LAMC2, TGF-β1, SMAD2, SMAD3, (L) Relative expression of protein LAMC2, TGF-β1, SMAD2, SMAD3. Compared to model, * P < 0.05, ** P < 0.01. For panels A-C, n = 6 independent animals per group; for panels (D–M) , n=3 independent animals per group.

    Journal: Frontiers in Physiology

    Article Title: Molecular mechanism of Danshen injection in treating endometrial fibrosis induced by intrauterine adhesions via the LAMC2-CD44-TGF-β1-SMAD2/3 signaling pathway

    doi: 10.3389/fphys.2026.1794215

    Figure Lengend Snippet: Danshen injection improves endometrial fibrosis in IUA rats by inhibiting the LAMC2-CD44-TGF-β1- SMAD2/3 signaling pathway. (A) Uterine Weight, (B) Uterine Length, (C) Grading of intrauterine adhesions in each group, (D) Number of uterine glands, (E) Collagen volume fraction, (F) H&E Staining, (G) MASSON Staining, (H) Immunofluorescence staining of COL1A1, (I) Immunofluorescence staining of COL3A1, (J) Immunofluorescence staining of α-SMA, (K) Mean fluorescence intensity of COL1A1, COL3A1 and α-SMA, L: WB detection of LAMC2, TGF-β1, SMAD2, SMAD3, (L) Relative expression of protein LAMC2, TGF-β1, SMAD2, SMAD3. Compared to model, * P < 0.05, ** P < 0.01. For panels A-C, n = 6 independent animals per group; for panels (D–M) , n=3 independent animals per group.

    Article Snippet: Primary antibodies: CK-19 (1:1000; YM8269, Immunoway, USA), Vimentin (1:1000; YM8324, Immunoway, USA), GAPDH (1:1000; A19056, ABclonal, China), LAMC2 (1:1000; A1869, ABclonal, China), E-cad (1:1000; A20798, ABclonal, China), N-cad (1:500; A0433, ABclonal, China), α-SMA (1:1000; A2319, ABclonal, China), TGF-β1 (1:2000; A15103, ABclonal, China), SMAD2 (1:5000; bsm-52223R, Bioss, China), SMAD3 (1:1000; A16913, ABclonal, China), p- SMAD2 (1:5000; bs-3419R, Bioss, China), p- SMAD3 (1:2000; Ap0727, ABclonal, China), and a secondary antibody (1:2000; AS014, ABclonal, China).

    Techniques: Injection, Staining, Immunofluorescence, Fluorescence, Expressing