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rabbit anti rat smad7  (Proteintech)


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    Structured Review

    Proteintech rabbit anti rat smad7
    Figure 11: Protein expression levels of hepatic TGF-𝛽1, p-Smad2, Smad2, p-Smad3, Smad3, and <t>Smad7.</t> Notes: A: blank control group (distilled water); B: model control group (distilled water); C: positive control group (3 g/kg⋅bw/day, positive medicine); D: low dose group (0.333 g/kg⋅bw/day, PSSS compound); E: medium dose group (0.667 g/kg⋅bw/day, PSSS compound); F: High dose group (1 g/kg⋅bw/day, PSSS compound). TGF-𝛽1, transforming growth factor-𝛽1.
    Rabbit Anti Rat Smad7, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 142 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+rat+smad7/SMAD7+Antibody/pm31118972-88-48-53
    Average 95 stars, based on 142 article reviews
    rabbit anti rat smad7 - by Bioz Stars, 2026-09
    95/100 stars

    Images

    1) Product Images from "A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF- β 1/Smad Signaling Pathway."

    Article Title: A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF- β 1/Smad Signaling Pathway.

    Journal: Evidence-based complementary and alternative medicine : eCAM

    doi: 10.1155/2019/9121347

    Figure 11: Protein expression levels of hepatic TGF-𝛽1, p-Smad2, Smad2, p-Smad3, Smad3, and Smad7. Notes: A: blank control group (distilled water); B: model control group (distilled water); C: positive control group (3 g/kg⋅bw/day, positive medicine); D: low dose group (0.333 g/kg⋅bw/day, PSSS compound); E: medium dose group (0.667 g/kg⋅bw/day, PSSS compound); F: High dose group (1 g/kg⋅bw/day, PSSS compound). TGF-𝛽1, transforming growth factor-𝛽1.
    Figure Legend Snippet: Figure 11: Protein expression levels of hepatic TGF-𝛽1, p-Smad2, Smad2, p-Smad3, Smad3, and Smad7. Notes: A: blank control group (distilled water); B: model control group (distilled water); C: positive control group (3 g/kg⋅bw/day, positive medicine); D: low dose group (0.333 g/kg⋅bw/day, PSSS compound); E: medium dose group (0.667 g/kg⋅bw/day, PSSS compound); F: High dose group (1 g/kg⋅bw/day, PSSS compound). TGF-𝛽1, transforming growth factor-𝛽1.

    Techniques Used: Expressing, Control, Positive Control

    Related Articles

    Saline:

    Article Title: A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF- β 1/Smad Signaling Pathway
    Article Snippet: Proteins were separated by 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel and transferred onto polyvinylidene fluoride (PVDF) membranes (Millipore, USA). .. PVDF membranes were blocked in 5% bovine serum albumin dissolved in tris-buffered saline containing Tween-20 (TBST) for 2 h and then incubated in primary rabbit anti-rat TGF- β 1 (monoclonal, 1:1000, Abcam, USA), rabbit anti-rat p-Smad2, rabbit anti-rat Smad2, rabbit anti-rat p-Smad3, rabbit anti-rat Smad3 (all monoclonal, 1:1000, CST, USA), rabbit anti-rat Smad7 (polyclonal, 1:1000, Proteintech group, Wuhan, China), and rabbit anti-rat GADPH (polyclonal, 1:10000, Proteintech group, Wuhan, China) overnight at 4°C. .. After washing by TBST, the membranes were incubated with HRP-conjugated affinipure goat anti-rabbit secondary antibodies (1:1000, Proteintech group, Wuhan, China) for 1 h. Subsequently, proteins were visualized with enhanced chemiluminescence solution (Millipore, USA) and BIO-RAD ChemiDoc XRS+.

    Article Title: A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF- β 1/Smad Signaling Pathway.
    Article Snippet: Proteins were separated by 10% sodium dodecyl sulfatepolyacrylamide gel electrophoresis gel and transferred onto polyvinylidene fluoride (PVDF) membranes (Millipore, USA). .. PVDF membranes were blocked in 5% bovine serum albumin dissolved in tris-buffered saline containing Tween20 (TBST) for 2 h and then incubated in primary rabbit antirat TGF-β1 (monoclonal, 1:1000, Abcam, USA), rabbit antirat p-Smad2, rabbit anti-rat Smad2, rabbit anti-rat p-Smad3, rabbit anti-rat Smad3 (all monoclonal, 1:1000, CST, USA), rabbit anti-rat Smad7 (polyclonal, 1:1000, Proteintech group, Wuhan, China), and rabbit anti-rat GADPH (polyclonal, 1:10000, Proteintech group, Wuhan, China) overnight at 4∘C. .. After washing by TBST, the membranes were incubated with HRP-conjugated affinipure goat anti-rabbit secondary antibodies (1:1000, Proteintech group, Wuhan, China) for 1 h. Subsequently, proteins were visualized with enhanced chemiluminescence solution (Millipore, USA) and BIO-RAD ChemiDoc XRS+.

    Incubation:

    Article Title: A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF- β 1/Smad Signaling Pathway
    Article Snippet: Proteins were separated by 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel and transferred onto polyvinylidene fluoride (PVDF) membranes (Millipore, USA). .. PVDF membranes were blocked in 5% bovine serum albumin dissolved in tris-buffered saline containing Tween-20 (TBST) for 2 h and then incubated in primary rabbit anti-rat TGF- β 1 (monoclonal, 1:1000, Abcam, USA), rabbit anti-rat p-Smad2, rabbit anti-rat Smad2, rabbit anti-rat p-Smad3, rabbit anti-rat Smad3 (all monoclonal, 1:1000, CST, USA), rabbit anti-rat Smad7 (polyclonal, 1:1000, Proteintech group, Wuhan, China), and rabbit anti-rat GADPH (polyclonal, 1:10000, Proteintech group, Wuhan, China) overnight at 4°C. .. After washing by TBST, the membranes were incubated with HRP-conjugated affinipure goat anti-rabbit secondary antibodies (1:1000, Proteintech group, Wuhan, China) for 1 h. Subsequently, proteins were visualized with enhanced chemiluminescence solution (Millipore, USA) and BIO-RAD ChemiDoc XRS+.

    Article Title: A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF- β 1/Smad Signaling Pathway.
    Article Snippet: Proteins were separated by 10% sodium dodecyl sulfatepolyacrylamide gel electrophoresis gel and transferred onto polyvinylidene fluoride (PVDF) membranes (Millipore, USA). .. PVDF membranes were blocked in 5% bovine serum albumin dissolved in tris-buffered saline containing Tween20 (TBST) for 2 h and then incubated in primary rabbit antirat TGF-β1 (monoclonal, 1:1000, Abcam, USA), rabbit antirat p-Smad2, rabbit anti-rat Smad2, rabbit anti-rat p-Smad3, rabbit anti-rat Smad3 (all monoclonal, 1:1000, CST, USA), rabbit anti-rat Smad7 (polyclonal, 1:1000, Proteintech group, Wuhan, China), and rabbit anti-rat GADPH (polyclonal, 1:10000, Proteintech group, Wuhan, China) overnight at 4∘C. .. After washing by TBST, the membranes were incubated with HRP-conjugated affinipure goat anti-rabbit secondary antibodies (1:1000, Proteintech group, Wuhan, China) for 1 h. Subsequently, proteins were visualized with enhanced chemiluminescence solution (Millipore, USA) and BIO-RAD ChemiDoc XRS+.



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    Figure 11: Protein expression levels of hepatic TGF-𝛽1, p-Smad2, Smad2, p-Smad3, Smad3, and <t>Smad7.</t> Notes: A: blank control group (distilled water); B: model control group (distilled water); C: positive control group (3 g/kg⋅bw/day, positive medicine); D: low dose group (0.333 g/kg⋅bw/day, PSSS compound); E: medium dose group (0.667 g/kg⋅bw/day, PSSS compound); F: High dose group (1 g/kg⋅bw/day, PSSS compound). TGF-𝛽1, transforming growth factor-𝛽1.
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    Image Search Results


    Primers for quantitative PCR analysis

    Journal: International Journal of Clinical and Experimental Pathology

    Article Title: Centella asiatica inhibits renal interstitial fibrosis by regulating Smad3 and Smad7 expression in the TGFβ signaling pathway

    doi:

    Figure Lengend Snippet: Primers for quantitative PCR analysis

    Article Snippet: The slides were incubated with primary antibodies of the rabbit anti-rat Smad3 and Smad7 (1:100; Bioss, Beijing, China) overnight at 4°C.

    Techniques: Real-time Polymerase Chain Reaction, Sequencing

    Treatment of CA inhibited Smad3 expression and increased Smad7 expression in the renal tissues of the UUO rats. CA or vehicle control was orally administered in sham- or UUO-operated rats starting on the day of the surgery for 14 days. A. Representative photomicrographs show the immuno-histochemical results of each group (400×). B. Quantification of Smad3 and Smad7 expression in each group. Error bars represent mean ± SD. *P<0.05 compared with Smad3 in sham group; #P<0.05 compared with Smad3 in UUO group; +P<0.05 compared with Smad7 in sham group; &P<0.05 compared with Smad7 in UUO group.

    Journal: International Journal of Clinical and Experimental Pathology

    Article Title: Centella asiatica inhibits renal interstitial fibrosis by regulating Smad3 and Smad7 expression in the TGFβ signaling pathway

    doi:

    Figure Lengend Snippet: Treatment of CA inhibited Smad3 expression and increased Smad7 expression in the renal tissues of the UUO rats. CA or vehicle control was orally administered in sham- or UUO-operated rats starting on the day of the surgery for 14 days. A. Representative photomicrographs show the immuno-histochemical results of each group (400×). B. Quantification of Smad3 and Smad7 expression in each group. Error bars represent mean ± SD. *P<0.05 compared with Smad3 in sham group; #P<0.05 compared with Smad3 in UUO group; +P<0.05 compared with Smad7 in sham group; &P<0.05 compared with Smad7 in UUO group.

    Article Snippet: The slides were incubated with primary antibodies of the rabbit anti-rat Smad3 and Smad7 (1:100; Bioss, Beijing, China) overnight at 4°C.

    Techniques: Expressing

     Smad3  mRNA and protein expression in each group (mean ± SD)

    Journal: International Journal of Clinical and Experimental Pathology

    Article Title: Centella asiatica inhibits renal interstitial fibrosis by regulating Smad3 and Smad7 expression in the TGFβ signaling pathway

    doi:

    Figure Lengend Snippet: Smad3 mRNA and protein expression in each group (mean ± SD)

    Article Snippet: The slides were incubated with primary antibodies of the rabbit anti-rat Smad3 and Smad7 (1:100; Bioss, Beijing, China) overnight at 4°C.

    Techniques: Expressing

    Treatment of CA inhibited Smad3 gene and protein expression in the renal tissues of the UUO rats. CA or vehicle control was orally administered in sham- or UUO-operated rats starting on the day of the surgery for 14 days. A. Smad3 was measured by the Western Blot; B. Quantitative data of the Smad3 mRNA and protein expression analyzed for each group. The error bars represent mean ± SD. *P<0.05 compared with Smad3 mRNA level in sham group; #P<0.05 compared with Smad3 mRNA level in UUO group; +P<0.05 compared with Smad3 protein level in sham group; &P<0.05 compared with Smad3 protein level in UUO group.

    Journal: International Journal of Clinical and Experimental Pathology

    Article Title: Centella asiatica inhibits renal interstitial fibrosis by regulating Smad3 and Smad7 expression in the TGFβ signaling pathway

    doi:

    Figure Lengend Snippet: Treatment of CA inhibited Smad3 gene and protein expression in the renal tissues of the UUO rats. CA or vehicle control was orally administered in sham- or UUO-operated rats starting on the day of the surgery for 14 days. A. Smad3 was measured by the Western Blot; B. Quantitative data of the Smad3 mRNA and protein expression analyzed for each group. The error bars represent mean ± SD. *P<0.05 compared with Smad3 mRNA level in sham group; #P<0.05 compared with Smad3 mRNA level in UUO group; +P<0.05 compared with Smad3 protein level in sham group; &P<0.05 compared with Smad3 protein level in UUO group.

    Article Snippet: The slides were incubated with primary antibodies of the rabbit anti-rat Smad3 and Smad7 (1:100; Bioss, Beijing, China) overnight at 4°C.

    Techniques: Expressing, Western Blot

    (a, b) Representative images of immunofluorescence staining of Smad 2/3 and Smad 7 on day 7 and day 14. (c, d) Mean fluorescence intensity (MFI) of Smad2/3 and Smad7 on day 7 and day 14, respectively. (n = 3, ∗∗∗∗p < 0.0001). (e–g) Western blot analysis and quantitative of protein expressions (Smad2/3 and Smad7) on day 7, 14. (H) Molecular mechanism of pSBLA2 hydrogel in preventing postoperative abdominal adhesions. (Created with BioRender.com ).

    Journal: Materials Today Bio

    Article Title: Zwitterion nanocomposite hydrogels with bioactivity and anti-adhesion properties for rapid prevention of postoperative and recurrent adhesion

    doi: 10.1016/j.mtbio.2025.101811

    Figure Lengend Snippet: (a, b) Representative images of immunofluorescence staining of Smad 2/3 and Smad 7 on day 7 and day 14. (c, d) Mean fluorescence intensity (MFI) of Smad2/3 and Smad7 on day 7 and day 14, respectively. (n = 3, ∗∗∗∗p < 0.0001). (e–g) Western blot analysis and quantitative of protein expressions (Smad2/3 and Smad7) on day 7, 14. (H) Molecular mechanism of pSBLA2 hydrogel in preventing postoperative abdominal adhesions. (Created with BioRender.com ).

    Article Snippet: Rabbit anti-rat Smad7 antibodies were obtained from Sanying Biotechnology.

    Techniques: Immunofluorescence, Staining, Fluorescence, Western Blot

    Figure 11: Protein expression levels of hepatic TGF-𝛽1, p-Smad2, Smad2, p-Smad3, Smad3, and Smad7. Notes: A: blank control group (distilled water); B: model control group (distilled water); C: positive control group (3 g/kg⋅bw/day, positive medicine); D: low dose group (0.333 g/kg⋅bw/day, PSSS compound); E: medium dose group (0.667 g/kg⋅bw/day, PSSS compound); F: High dose group (1 g/kg⋅bw/day, PSSS compound). TGF-𝛽1, transforming growth factor-𝛽1.

    Journal: Evidence-based complementary and alternative medicine : eCAM

    Article Title: A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF- β 1/Smad Signaling Pathway.

    doi: 10.1155/2019/9121347

    Figure Lengend Snippet: Figure 11: Protein expression levels of hepatic TGF-𝛽1, p-Smad2, Smad2, p-Smad3, Smad3, and Smad7. Notes: A: blank control group (distilled water); B: model control group (distilled water); C: positive control group (3 g/kg⋅bw/day, positive medicine); D: low dose group (0.333 g/kg⋅bw/day, PSSS compound); E: medium dose group (0.667 g/kg⋅bw/day, PSSS compound); F: High dose group (1 g/kg⋅bw/day, PSSS compound). TGF-𝛽1, transforming growth factor-𝛽1.

    Article Snippet: PVDF membranes were blocked in 5% bovine serum albumin dissolved in tris-buffered saline containing Tween20 (TBST) for 2 h and then incubated in primary rabbit antirat TGF-β1 (monoclonal, 1:1000, Abcam, USA), rabbit antirat p-Smad2, rabbit anti-rat Smad2, rabbit anti-rat p-Smad3, rabbit anti-rat Smad3 (all monoclonal, 1:1000, CST, USA), rabbit anti-rat Smad7 (polyclonal, 1:1000, Proteintech group, Wuhan, China), and rabbit anti-rat GADPH (polyclonal, 1:10000, Proteintech group, Wuhan, China) overnight at 4∘C.

    Techniques: Expressing, Control, Positive Control

    Reverse transcription-quantitative polymerase chain reaction primer sequences.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Reverse transcription-quantitative polymerase chain reaction primer sequences.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques: Polymerase Chain Reaction, Sequencing

    Target association verification between miR-20b-5p and Smad7. (A) Predicted binding site of miR-20b-5p in the Smad7 3′UTR. (B) Detection of luciferase activity by dual luciferase reporter gene assays. * P<0.05, compared with the NC group. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; mut, mutant; wt, wild-type; NC, negative control.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Target association verification between miR-20b-5p and Smad7. (A) Predicted binding site of miR-20b-5p in the Smad7 3′UTR. (B) Detection of luciferase activity by dual luciferase reporter gene assays. * P<0.05, compared with the NC group. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; mut, mutant; wt, wild-type; NC, negative control.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques: Binding Assay, Luciferase, Activity Assay, Mutagenesis, Negative Control

    Survival rates of rats.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Survival rates of rats.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques:

    Results of LVEDV, LVEDD, LVESV and LVESD by echocardiography (n=5).

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Results of LVEDV, LVEDD, LVESV and LVESD by echocardiography (n=5).

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques:

    Echocardiograph results of LVEEF and LVEFS (n=5).

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Echocardiograph results of LVEEF and LVEFS (n=5).

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques:

    Echocardiograph results of LVESP and LVEDP (n=5).

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Echocardiograph results of LVESP and LVEDP (n=5).

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques:

    Myocardial infarct size in rats in each group. (A) Triphenyltetrazolium chloride staining results of rats in each group. (B) Comparison of myocardial infarct size in rats in each group. * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR, ischemia-reperfusion; INFS, infarct size.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Myocardial infarct size in rats in each group. (A) Triphenyltetrazolium chloride staining results of rats in each group. (B) Comparison of myocardial infarct size in rats in each group. * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR, ischemia-reperfusion; INFS, infarct size.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques: Staining, Small Interfering RNA, Negative Control

    Ultrastructure of cardiomyocytes in rats in each group (n=3). Images at magnification, ×3,000. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR, ischemia-reperfusion.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Ultrastructure of cardiomyocytes in rats in each group (n=3). Images at magnification, ×3,000. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR, ischemia-reperfusion.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques: Small Interfering RNA, Negative Control

    Hematoxylin and eosin staining of the myocardium in rats in each group (n=3). Images at magnification, ×200. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR, ischemia-reperfusion.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Hematoxylin and eosin staining of the myocardium in rats in each group (n=3). Images at magnification, ×200. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR, ischemia-reperfusion.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques: Staining, Small Interfering RNA, Negative Control

    Masson's staining of myocardial tissue from rats in each group. (A) Masson's staining of myocardial tissue from rats in each group (magnification, ×400). (B) Changes in CVF and PVCA in rats in each group are shown in a bar graph. * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group. CVF, myocardial collagen volume fraction; PVCA, perivascular collagen area; miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR, ischemia-reperfusion.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Masson's staining of myocardial tissue from rats in each group. (A) Masson's staining of myocardial tissue from rats in each group (magnification, ×400). (B) Changes in CVF and PVCA in rats in each group are shown in a bar graph. * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group. CVF, myocardial collagen volume fraction; PVCA, perivascular collagen area; miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR, ischemia-reperfusion.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques: Staining, Small Interfering RNA, Negative Control

    Immunohistochemical results of rats in each group (n=3). (A) Immunohistochemical results (magnification, ×400). (B) Comparison of the Smad7-positive rate among all rat groups. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR; ischemia-reperfusion; * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Immunohistochemical results of rats in each group (n=3). (A) Immunohistochemical results (magnification, ×400). (B) Comparison of the Smad7-positive rate among all rat groups. miR-20b-5p, microRNA-20b-5p; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; NC, negative control; IR; ischemia-reperfusion; * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques: Immunohistochemical staining, Small Interfering RNA, Negative Control

    Expression of miR-20b-5p and mRNA expression of TGF-β1/Smad signaling pathway-related proteins in myocardial tissue from rats in each group. * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group. miR-20b-5p, microRNA-20b-5p; Smad3, small mothers against decapentaplegic homolog 3; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; TGF-β1, transforming growth factor-β1; NC, negative control; IR, ischemia-reperfusion.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Expression of miR-20b-5p and mRNA expression of TGF-β1/Smad signaling pathway-related proteins in myocardial tissue from rats in each group. * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group. miR-20b-5p, microRNA-20b-5p; Smad3, small mothers against decapentaplegic homolog 3; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; TGF-β1, transforming growth factor-β1; NC, negative control; IR, ischemia-reperfusion.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques: Expressing, Small Interfering RNA, Negative Control

    Expression of TGF-β1/Smad signaling pathway components in myocardial tissue from rats in each group. (A) Banding diagram of the expression of TGF-β1/Smad signaling pathway components in myocardial tissue from rats in each group, (B) Histogram of the expression of TGF-β1/Smad signaling pathway components in myocardial tissue from rats in each group. * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group. miR-20b-5p, microRNA-20b-5p; Smad3, small mothers against decapentaplegic homolog 3; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; TGF-β1, transforming growth factor-β1; NC, negative control; IR, ischemia-reperfusion.

    Journal: International Journal of Molecular Medicine

    Article Title: MicroRNA-20b-5p promotes ventricular remodeling by targeting the TGF-β/Smad signaling pathway in a rat model of ischemia-reperfusion injury

    doi: 10.3892/ijmm.2018.3695

    Figure Lengend Snippet: Expression of TGF-β1/Smad signaling pathway components in myocardial tissue from rats in each group. (A) Banding diagram of the expression of TGF-β1/Smad signaling pathway components in myocardial tissue from rats in each group, (B) Histogram of the expression of TGF-β1/Smad signaling pathway components in myocardial tissue from rats in each group. * P<0.05, compared with the sham group; # P<0.05, compared with the IR group; & P<0.05, compared with the miR-20b-5p inhibitors + si-Smad7 group. miR-20b-5p, microRNA-20b-5p; Smad3, small mothers against decapentaplegic homolog 3; Smad7, small mothers against decapentaplegic homolog 7; si-, small interfering RNA; TGF-β1, transforming growth factor-β1; NC, negative control; IR, ischemia-reperfusion.

    Article Snippet: According to the conventional method of immunohistochemical staining, following the elimination of endogenous peroxidase activity in 0.3% H 2 O 2 − methanol solution at room temperature for 10 min, a 1:100 dilution of rabbit anti-rat Smad7 antibody (cat. no. BA1399; 1:100; Wuhan Boster Biological Technology Co., Ltd., Wuhan, China) was added to the cardiac tissue for 16 h at 4°C.

    Techniques: Expressing, Small Interfering RNA, Negative Control