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tgf β1 rabbit polyclonal antibody  (Proteintech)


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    Proteintech tgf β1 rabbit polyclonal antibody
    Tgf β1 Rabbit Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1112 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tgf+%CE%B21+rabbit+polyclonal+antibody/pm41407243-151-18-23?v=Proteintech
    Average 96 stars, based on 1112 article reviews
    tgf β1 rabbit polyclonal antibody - by Bioz Stars, 2026-08
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    Mechanism diagram of moxibustion intervention in gastric cancer mice for immune regulation and anti-tumor effects. Moxibustion can reverse tumor immune escape and enhance the immune function of the body by regulating and reducing the proportion of CD4 + CD25+Foxp3+Treg cells in the blood and the expression levels of IL-10 and <t>TGF-β1.</t> The acupoints for the corresponding experimental mice are Zhongwan (CV12), Qihai (CV6), Guanyuan (CV4), and Zusanli (ST36).
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    Proteintech rabbit polyclonal antibodies against tgf β1
    Intratracheal administration of PS-MPs induced pulmonary fibrosis in rats. Masson’s trichrome staining revealed green collagen deposition in the rat lungs ( A , C ). The expression levels of <t>TGF-β1</t> ( B , D ) and p-Smad2 ( E , F ) increased, and the expression levels of p-Akt ( E , G ) and nuclear β-catenin ( E , H ) decreased in the lungs of the rats in the PS-MP exposure groups. Abbreviations for WB analysis are C: control, V: vehicle, L: 0.31 mg PS-MPs, H: 1.25 mg PS-MPs. All the results are expressed as the mean ± SD; n = 4. * p < 0.05, ** p < 0.01 vs. the control group; # p < 0.05, ## p < 0.01 vs. the vehicle group; bar = 100 μm.
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    Boster Bio polyclonal rabbit antihuman tgf β1
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    Proteintech anti tgf β1 rabbit polyclonal antibody
    Spatial transcriptome map of internal hemorrhoid tissue. A: Hematoxylin and eosin-stained section of internal hemorrhoid tissue; B: Spatial transcriptome; C: Differences in expression of the classic marker genes collagen 3 alpha 1, decorin, and actin alpha 2 in fibroblasts; D: Spatial localization of the classic marker genes collagen 3 alpha 1, decorin, and actin alpha 2 in fibroblasts; E: Spatial distribution of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth <t>factor-β1;</t> F: Differences in gene expression of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth factor-β1. COL3A1 : Collagen 3 alpha 1; DCN : Decorin; ACTA2 : Actin alpha 2; Sphk1 : Sphingosine kinase 1; S1PR1 : Sphingosine-1-phosphate receptor 1; <t>TGF-β1</t> : Transforming growth factor-β1.
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    Abbkine Inc rabbit polyclonal anti-tgf-β1 antibody
    F4/80, F4/80 stain; PAI-1, plasminogen activator inhibitor-1 stain; PAS, periodic acid-Schiff stain; STZ, streptozotocin; <t>TGF-β1,</t> transforming growth factor beta-1 stain. Original magnification, ×400.
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    Image Search Results


    Mechanism diagram of moxibustion intervention in gastric cancer mice for immune regulation and anti-tumor effects. Moxibustion can reverse tumor immune escape and enhance the immune function of the body by regulating and reducing the proportion of CD4 + CD25+Foxp3+Treg cells in the blood and the expression levels of IL-10 and TGF-β1. The acupoints for the corresponding experimental mice are Zhongwan (CV12), Qihai (CV6), Guanyuan (CV4), and Zusanli (ST36).

    Journal: Frontiers in Pharmacology

    Article Title: Moxibustion combined with chemotherapy inhibits gastric cancer growth by modulating the immunosuppressive microenvironment involving the Treg/IL-10/TGF-β1 axis

    doi: 10.3389/fphar.2025.1688182

    Figure Lengend Snippet: Mechanism diagram of moxibustion intervention in gastric cancer mice for immune regulation and anti-tumor effects. Moxibustion can reverse tumor immune escape and enhance the immune function of the body by regulating and reducing the proportion of CD4 + CD25+Foxp3+Treg cells in the blood and the expression levels of IL-10 and TGF-β1. The acupoints for the corresponding experimental mice are Zhongwan (CV12), Qihai (CV6), Guanyuan (CV4), and Zusanli (ST36).

    Article Snippet: The primary antibodies and their dilution ratios were as follows: rabbit polyclonal antibody against Foxp3 (Bioss, cat. Bs-23074R, lot: AF03154485), diluted 1:1,000; rabbit polyclonal antibody against TGF-β1 (Bioss, cat. Bs-0086R, lot: AG19301,531), diluted 1:2000; mouse monoclonal antibody against GAPDH (Zhongshan Jinqiao, cat. TA-08, lot: 230040220), diluted 1:2000.

    Techniques: Expressing

    Correlation analysis among FOXP3, IL-10, and TGF-β1 in gastric cancer. In gastric cancer tissues, FOXP3, IL-10 and TGFβ1 are all associated with immune cells to varying degrees (A) , and have a strong association with Treg cells (B) .

    Journal: Frontiers in Pharmacology

    Article Title: Moxibustion combined with chemotherapy inhibits gastric cancer growth by modulating the immunosuppressive microenvironment involving the Treg/IL-10/TGF-β1 axis

    doi: 10.3389/fphar.2025.1688182

    Figure Lengend Snippet: Correlation analysis among FOXP3, IL-10, and TGF-β1 in gastric cancer. In gastric cancer tissues, FOXP3, IL-10 and TGFβ1 are all associated with immune cells to varying degrees (A) , and have a strong association with Treg cells (B) .

    Article Snippet: The primary antibodies and their dilution ratios were as follows: rabbit polyclonal antibody against Foxp3 (Bioss, cat. Bs-23074R, lot: AF03154485), diluted 1:1,000; rabbit polyclonal antibody against TGF-β1 (Bioss, cat. Bs-0086R, lot: AG19301,531), diluted 1:2000; mouse monoclonal antibody against GAPDH (Zhongshan Jinqiao, cat. TA-08, lot: 230040220), diluted 1:2000.

    Techniques:

    Experimental results in mice. (A) Grouped appearance images of nude mice, showing the general conditions of the model group, moxibustion group, chemotherapy group, and moxibustion combined with chemotherapy group. (B) Gross specimens of tumor tissues from each group of nude mice, comparing the size and shape differences of tumors in each group through a ruler. The two sub-figures have visual proportion differences due to different shooting distances; the actual size should be based on the scale and quantitative data. (C) The changes in tumor volume of each group of mice. The horizontal axis represents the number of days of observation after mouse modeling, and the vertical axis indicates the size of the tumor volume. The expression differences began to be shown from the 12th day as illustrated in the figure. The significant differences between groups are indicated by the letter method. If the letters are the same, it means there is no statistical difference between the two groups; otherwise, there is a difference (p < 0.05). (A) compared with the model group; (B) compared with the moxibustion group; (C) compared with the chemotherapy group. Model group: 32.01 ± 5.49 mm 3 , 92.19 ± 20.40 mm 3 , 157.30 ± 28.79 mm 3 , 276.10 ± 76.86 mm 3 . Moxibustion group: 32.96 ± 2.93 mm 3 , 51.29 ± 12.55 mm 3 , 85.08 ± 17.83 mm 3 , 182.55 ± 15.40 mm 3 . Chemotherapy group: 30.36 ± 7.72 mm 3 , 37.97 ± 15.11 mm 3 , 68.57 ± 15.09 mm 3 , 123.15 ± 36.76 mm 3 . Moxibustion combined with chemotherapy group: 26.39 ± 10.52 mm 3 , 31.50 ± 8.50 mm 3 , 43.53 ± 14.24 mm 3 , 64.09 ± 17.86 mm 3 . There were significant differences in tumor volume among the groups of mice (overall between-group effect: F (3,20) = 90.502, p < 0.001, partial η 2 = 0.931). Post hoc comparisons, with the moxibustion plus chemotherapy group as the reference, showed that on the ninth day, the tumor volume of the model group and the moxibustion group was significantly larger than that of the moxibustion plus chemotherapy group (both p < 0.05); by the 12th day, the tumor volume of the chemotherapy group was also significantly larger than that of the moxibustion plus chemotherapy group (p = 0.041); on the 15th day, the tumor volume of all single-treatment groups was extremely significantly larger than that of the moxibustion plus chemotherapy group (model group vs. combined group: p < 0.001; moxibustion group vs. combined group: p < 0.001; chemotherapy group vs. combined group: p = 0.031). (D) HE staining pathological sections of tumor tissues from each group (upper: low-power field; lower: high-power field of the selected area). (E) Protein expression of FOXP3 and TGF-β1 in tumor tissues. (a) Protein molecular weight standard. (b) Representative results of three independent repeated experiments detected by Western blot. The letters A-E above the bands represent the blank control group, model group, moxibustion group, chemotherapy group, and combined treatment group, respectively. (c–d) Semi-quantitative statistical analysis of FOXP3 (c) and TGF-β1 (d) protein expression. The data were calculated by the ratio of the gray value of the target protein to GAPDH and expressed as mean ± standard deviation. *p < 0.05, **p < 0.01, ***p < 0.001 (α = 0.05).

    Journal: Frontiers in Pharmacology

    Article Title: Moxibustion combined with chemotherapy inhibits gastric cancer growth by modulating the immunosuppressive microenvironment involving the Treg/IL-10/TGF-β1 axis

    doi: 10.3389/fphar.2025.1688182

    Figure Lengend Snippet: Experimental results in mice. (A) Grouped appearance images of nude mice, showing the general conditions of the model group, moxibustion group, chemotherapy group, and moxibustion combined with chemotherapy group. (B) Gross specimens of tumor tissues from each group of nude mice, comparing the size and shape differences of tumors in each group through a ruler. The two sub-figures have visual proportion differences due to different shooting distances; the actual size should be based on the scale and quantitative data. (C) The changes in tumor volume of each group of mice. The horizontal axis represents the number of days of observation after mouse modeling, and the vertical axis indicates the size of the tumor volume. The expression differences began to be shown from the 12th day as illustrated in the figure. The significant differences between groups are indicated by the letter method. If the letters are the same, it means there is no statistical difference between the two groups; otherwise, there is a difference (p < 0.05). (A) compared with the model group; (B) compared with the moxibustion group; (C) compared with the chemotherapy group. Model group: 32.01 ± 5.49 mm 3 , 92.19 ± 20.40 mm 3 , 157.30 ± 28.79 mm 3 , 276.10 ± 76.86 mm 3 . Moxibustion group: 32.96 ± 2.93 mm 3 , 51.29 ± 12.55 mm 3 , 85.08 ± 17.83 mm 3 , 182.55 ± 15.40 mm 3 . Chemotherapy group: 30.36 ± 7.72 mm 3 , 37.97 ± 15.11 mm 3 , 68.57 ± 15.09 mm 3 , 123.15 ± 36.76 mm 3 . Moxibustion combined with chemotherapy group: 26.39 ± 10.52 mm 3 , 31.50 ± 8.50 mm 3 , 43.53 ± 14.24 mm 3 , 64.09 ± 17.86 mm 3 . There were significant differences in tumor volume among the groups of mice (overall between-group effect: F (3,20) = 90.502, p < 0.001, partial η 2 = 0.931). Post hoc comparisons, with the moxibustion plus chemotherapy group as the reference, showed that on the ninth day, the tumor volume of the model group and the moxibustion group was significantly larger than that of the moxibustion plus chemotherapy group (both p < 0.05); by the 12th day, the tumor volume of the chemotherapy group was also significantly larger than that of the moxibustion plus chemotherapy group (p = 0.041); on the 15th day, the tumor volume of all single-treatment groups was extremely significantly larger than that of the moxibustion plus chemotherapy group (model group vs. combined group: p < 0.001; moxibustion group vs. combined group: p < 0.001; chemotherapy group vs. combined group: p = 0.031). (D) HE staining pathological sections of tumor tissues from each group (upper: low-power field; lower: high-power field of the selected area). (E) Protein expression of FOXP3 and TGF-β1 in tumor tissues. (a) Protein molecular weight standard. (b) Representative results of three independent repeated experiments detected by Western blot. The letters A-E above the bands represent the blank control group, model group, moxibustion group, chemotherapy group, and combined treatment group, respectively. (c–d) Semi-quantitative statistical analysis of FOXP3 (c) and TGF-β1 (d) protein expression. The data were calculated by the ratio of the gray value of the target protein to GAPDH and expressed as mean ± standard deviation. *p < 0.05, **p < 0.01, ***p < 0.001 (α = 0.05).

    Article Snippet: The primary antibodies and their dilution ratios were as follows: rabbit polyclonal antibody against Foxp3 (Bioss, cat. Bs-23074R, lot: AF03154485), diluted 1:1,000; rabbit polyclonal antibody against TGF-β1 (Bioss, cat. Bs-0086R, lot: AG19301,531), diluted 1:2000; mouse monoclonal antibody against GAPDH (Zhongshan Jinqiao, cat. TA-08, lot: 230040220), diluted 1:2000.

    Techniques: Expressing, Staining, Molecular Weight, Western Blot, Control, Standard Deviation

    The effects on the expression of FOXP3+ Treg in the tumor microenvironment and key inhibitory factors in the peripheral blood of mice in each group. (A) Representative flow cytometry dot plots of the proportion of CD4 + CD25+FOXP3+ regulatory T (Treg) cells in the peripheral blood of each group of mice. The cell gating strategy was based on the consensus marker scheme for Treg cell analysis: first, the lymphocyte population was gated, followed by gating of CD4 + T cells and CD25 + cells in sequence, and finally the Treg cell population was determined by FOXP3+ cells. The model group was 7.49%, the moxibustion group was 5.42%, the chemotherapy group was 4.73%, and the moxibustion combined with chemotherapy group was 4.15%. (B) Comparison of CD4 + CD25 + FOXP3 + Treg, TGF-β1 and IL-10 levels in the serum of mice among different groups. A, B, C, and D represent different groups. The expression levels of Treg (%) in the model group, moxibustion group, chemotherapy group, and moxibustion combined with chemotherapy group were 7.02 ± 0.45, 5.59 ± 0.35, 4.73 ± 0.57, and 3.91 ± 0.21, respectively; the expression levels of TGF-β1 (pg/mL) were 547.84 ± 7.25, 325.24 ± 15.03, 322.05 ± 21.91, and 266.82 ± 13.71, respectively; the expression levels of IL-10 (pg/mL) were 127.21 ± 2.07, 101.68 ± 1.42, 84.53 ± 4.25, and 51.42 ± 3.65, respectively.

    Journal: Frontiers in Pharmacology

    Article Title: Moxibustion combined with chemotherapy inhibits gastric cancer growth by modulating the immunosuppressive microenvironment involving the Treg/IL-10/TGF-β1 axis

    doi: 10.3389/fphar.2025.1688182

    Figure Lengend Snippet: The effects on the expression of FOXP3+ Treg in the tumor microenvironment and key inhibitory factors in the peripheral blood of mice in each group. (A) Representative flow cytometry dot plots of the proportion of CD4 + CD25+FOXP3+ regulatory T (Treg) cells in the peripheral blood of each group of mice. The cell gating strategy was based on the consensus marker scheme for Treg cell analysis: first, the lymphocyte population was gated, followed by gating of CD4 + T cells and CD25 + cells in sequence, and finally the Treg cell population was determined by FOXP3+ cells. The model group was 7.49%, the moxibustion group was 5.42%, the chemotherapy group was 4.73%, and the moxibustion combined with chemotherapy group was 4.15%. (B) Comparison of CD4 + CD25 + FOXP3 + Treg, TGF-β1 and IL-10 levels in the serum of mice among different groups. A, B, C, and D represent different groups. The expression levels of Treg (%) in the model group, moxibustion group, chemotherapy group, and moxibustion combined with chemotherapy group were 7.02 ± 0.45, 5.59 ± 0.35, 4.73 ± 0.57, and 3.91 ± 0.21, respectively; the expression levels of TGF-β1 (pg/mL) were 547.84 ± 7.25, 325.24 ± 15.03, 322.05 ± 21.91, and 266.82 ± 13.71, respectively; the expression levels of IL-10 (pg/mL) were 127.21 ± 2.07, 101.68 ± 1.42, 84.53 ± 4.25, and 51.42 ± 3.65, respectively.

    Article Snippet: The primary antibodies and their dilution ratios were as follows: rabbit polyclonal antibody against Foxp3 (Bioss, cat. Bs-23074R, lot: AF03154485), diluted 1:1,000; rabbit polyclonal antibody against TGF-β1 (Bioss, cat. Bs-0086R, lot: AG19301,531), diluted 1:2000; mouse monoclonal antibody against GAPDH (Zhongshan Jinqiao, cat. TA-08, lot: 230040220), diluted 1:2000.

    Techniques: Expressing, Flow Cytometry, Marker, Cell Analysis, Sequencing, Comparison

    Intratracheal administration of PS-MPs induced pulmonary fibrosis in rats. Masson’s trichrome staining revealed green collagen deposition in the rat lungs ( A , C ). The expression levels of TGF-β1 ( B , D ) and p-Smad2 ( E , F ) increased, and the expression levels of p-Akt ( E , G ) and nuclear β-catenin ( E , H ) decreased in the lungs of the rats in the PS-MP exposure groups. Abbreviations for WB analysis are C: control, V: vehicle, L: 0.31 mg PS-MPs, H: 1.25 mg PS-MPs. All the results are expressed as the mean ± SD; n = 4. * p < 0.05, ** p < 0.01 vs. the control group; # p < 0.05, ## p < 0.01 vs. the vehicle group; bar = 100 μm.

    Journal: Toxics

    Article Title: Intratracheal Administration of Polystyrene Micro(nano)plastics with a Mixed Particle Size Promote Pulmonary Fibrosis in Rats by Activating TGF-β1 Signaling and Destabilizing Mitochondrial Dynamics and Mitophagy in a Dose- and Time-Dependent Manner

    doi: 10.3390/toxics13060487

    Figure Lengend Snippet: Intratracheal administration of PS-MPs induced pulmonary fibrosis in rats. Masson’s trichrome staining revealed green collagen deposition in the rat lungs ( A , C ). The expression levels of TGF-β1 ( B , D ) and p-Smad2 ( E , F ) increased, and the expression levels of p-Akt ( E , G ) and nuclear β-catenin ( E , H ) decreased in the lungs of the rats in the PS-MP exposure groups. Abbreviations for WB analysis are C: control, V: vehicle, L: 0.31 mg PS-MPs, H: 1.25 mg PS-MPs. All the results are expressed as the mean ± SD; n = 4. * p < 0.05, ** p < 0.01 vs. the control group; # p < 0.05, ## p < 0.01 vs. the vehicle group; bar = 100 μm.

    Article Snippet: Rabbit polyclonal antibodies against TGF-β1 (21898-1-AP), DRP1 (12957-1-AP), Mfn1 (13798-1-AP), Mfn2 (12186-1-AP), VDAC1 (55259-1-AP), and β-actin (81115-1-RR) were purchased from ProteinTech (Wuhan, China).

    Techniques: Staining, Expressing, Control

    Spatial transcriptome map of internal hemorrhoid tissue. A: Hematoxylin and eosin-stained section of internal hemorrhoid tissue; B: Spatial transcriptome; C: Differences in expression of the classic marker genes collagen 3 alpha 1, decorin, and actin alpha 2 in fibroblasts; D: Spatial localization of the classic marker genes collagen 3 alpha 1, decorin, and actin alpha 2 in fibroblasts; E: Spatial distribution of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth factor-β1; F: Differences in gene expression of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth factor-β1. COL3A1 : Collagen 3 alpha 1; DCN : Decorin; ACTA2 : Actin alpha 2; Sphk1 : Sphingosine kinase 1; S1PR1 : Sphingosine-1-phosphate receptor 1; TGF-β1 : Transforming growth factor-β1.

    Journal: World Journal of Gastrointestinal Surgery

    Article Title: Single-nucleus RNA sequencing and spatial transcriptomics reveal the mechanism by which Xiaozhiling injection treats internal hemorrhoids

    doi: 10.4240/wjgs.v17.i4.103494

    Figure Lengend Snippet: Spatial transcriptome map of internal hemorrhoid tissue. A: Hematoxylin and eosin-stained section of internal hemorrhoid tissue; B: Spatial transcriptome; C: Differences in expression of the classic marker genes collagen 3 alpha 1, decorin, and actin alpha 2 in fibroblasts; D: Spatial localization of the classic marker genes collagen 3 alpha 1, decorin, and actin alpha 2 in fibroblasts; E: Spatial distribution of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth factor-β1; F: Differences in gene expression of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth factor-β1. COL3A1 : Collagen 3 alpha 1; DCN : Decorin; ACTA2 : Actin alpha 2; Sphk1 : Sphingosine kinase 1; S1PR1 : Sphingosine-1-phosphate receptor 1; TGF-β1 : Transforming growth factor-β1.

    Article Snippet: Xiaozhiling injection (Beijing China Resources High-Tech Natural Medicine Co., Ltd.); inhaled isoflurane (Baxter Healthcare Corporation, China); 4% neutral formaldehyde fixative solution; 6% croton oil (Beijing Huawei Ruike Chemical Co., Ltd.); pyridine (Beijing Lambolide Trading Co., Ltd.); ether (Xilong Science Co., Ltd.); horseradish peroxidase-conjugated polyclonal anti-rabbit/mouse IgG (Boster); an anti-TGF-β1 rabbit polyclonal antibody (Proteintech); an anti-Sphk1 rabbit polyclonal antibody (Proteintech); an anti-sphingosine-1-phosphate receptor 1 (S1PR1) rabbit polyclonal antibody (Proteintech); and an alpha smooth muscle actin specific monoclonal antibody (Proteintech) were used in this study.

    Techniques: Staining, Expressing, Marker, Gene Expression

    Spatial transcriptome. A: Hematoxylin and eosin-stained section 1 week after Xiaozhiling injection; B: Spatial transcriptome; C: Differences in expression of the classic fibroblast marker genes collagen 3 alpha 1, decorin, and actin alpha 2 in different clusters; D: Spatial localization of the classic fibroblast marker genes collagen 3 alpha 1, decorin, and actin alpha 2; E: Spatial localization of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth factor-β1; F: Differences in expression of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth factor-β1 in different clusters; G: Analysis of differences between the two groups. COL3A1 : Collagen 3 alpha 1; DCN : Decorin; ACTA2 : Actin alpha 2; Sphk1: Sphingosine kinase 1; S1PR1: Sphingosine-1-phosphate receptor 1; TGF-β1: Transforming growth factor-β1.

    Journal: World Journal of Gastrointestinal Surgery

    Article Title: Single-nucleus RNA sequencing and spatial transcriptomics reveal the mechanism by which Xiaozhiling injection treats internal hemorrhoids

    doi: 10.4240/wjgs.v17.i4.103494

    Figure Lengend Snippet: Spatial transcriptome. A: Hematoxylin and eosin-stained section 1 week after Xiaozhiling injection; B: Spatial transcriptome; C: Differences in expression of the classic fibroblast marker genes collagen 3 alpha 1, decorin, and actin alpha 2 in different clusters; D: Spatial localization of the classic fibroblast marker genes collagen 3 alpha 1, decorin, and actin alpha 2; E: Spatial localization of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth factor-β1; F: Differences in expression of sphingosine kinase 1, sphingosine-1-phosphate receptor 1, and transforming growth factor-β1 in different clusters; G: Analysis of differences between the two groups. COL3A1 : Collagen 3 alpha 1; DCN : Decorin; ACTA2 : Actin alpha 2; Sphk1: Sphingosine kinase 1; S1PR1: Sphingosine-1-phosphate receptor 1; TGF-β1: Transforming growth factor-β1.

    Article Snippet: Xiaozhiling injection (Beijing China Resources High-Tech Natural Medicine Co., Ltd.); inhaled isoflurane (Baxter Healthcare Corporation, China); 4% neutral formaldehyde fixative solution; 6% croton oil (Beijing Huawei Ruike Chemical Co., Ltd.); pyridine (Beijing Lambolide Trading Co., Ltd.); ether (Xilong Science Co., Ltd.); horseradish peroxidase-conjugated polyclonal anti-rabbit/mouse IgG (Boster); an anti-TGF-β1 rabbit polyclonal antibody (Proteintech); an anti-Sphk1 rabbit polyclonal antibody (Proteintech); an anti-sphingosine-1-phosphate receptor 1 (S1PR1) rabbit polyclonal antibody (Proteintech); and an alpha smooth muscle actin specific monoclonal antibody (Proteintech) were used in this study.

    Techniques: Staining, Injection, Expressing, Marker

    Immunohistochemical staining of internal hemorrhoid tissue. A: Sphingosine kinase 1 (100 ×); B: Sphingosine-1-phosphate receptor 1 (100 ×); C: Transforming growth factor-β1 (100 ×); D: Sphingosine kinase 1 (400 ×); E: Sphingosine-1-phosphate receptor 1 (400 ×); F: Transforming growth factor-β1 (400 ×).

    Journal: World Journal of Gastrointestinal Surgery

    Article Title: Single-nucleus RNA sequencing and spatial transcriptomics reveal the mechanism by which Xiaozhiling injection treats internal hemorrhoids

    doi: 10.4240/wjgs.v17.i4.103494

    Figure Lengend Snippet: Immunohistochemical staining of internal hemorrhoid tissue. A: Sphingosine kinase 1 (100 ×); B: Sphingosine-1-phosphate receptor 1 (100 ×); C: Transforming growth factor-β1 (100 ×); D: Sphingosine kinase 1 (400 ×); E: Sphingosine-1-phosphate receptor 1 (400 ×); F: Transforming growth factor-β1 (400 ×).

    Article Snippet: Xiaozhiling injection (Beijing China Resources High-Tech Natural Medicine Co., Ltd.); inhaled isoflurane (Baxter Healthcare Corporation, China); 4% neutral formaldehyde fixative solution; 6% croton oil (Beijing Huawei Ruike Chemical Co., Ltd.); pyridine (Beijing Lambolide Trading Co., Ltd.); ether (Xilong Science Co., Ltd.); horseradish peroxidase-conjugated polyclonal anti-rabbit/mouse IgG (Boster); an anti-TGF-β1 rabbit polyclonal antibody (Proteintech); an anti-Sphk1 rabbit polyclonal antibody (Proteintech); an anti-sphingosine-1-phosphate receptor 1 (S1PR1) rabbit polyclonal antibody (Proteintech); and an alpha smooth muscle actin specific monoclonal antibody (Proteintech) were used in this study.

    Techniques: Immunohistochemical staining, Staining

    Immunohistochemical staining. A: Sphingosine kinase 1 (100 ×); B: Sphingosine-1-phosphate receptor 1 (100 ×); C: Transforming growth factor-β1 (100 ×); D: Sphingosine kinase 1 (400 ×); E: Sphingosine-1-phosphate receptor 1 (400 ×); F: Transforming growth factor-β1 (400 ×).

    Journal: World Journal of Gastrointestinal Surgery

    Article Title: Single-nucleus RNA sequencing and spatial transcriptomics reveal the mechanism by which Xiaozhiling injection treats internal hemorrhoids

    doi: 10.4240/wjgs.v17.i4.103494

    Figure Lengend Snippet: Immunohistochemical staining. A: Sphingosine kinase 1 (100 ×); B: Sphingosine-1-phosphate receptor 1 (100 ×); C: Transforming growth factor-β1 (100 ×); D: Sphingosine kinase 1 (400 ×); E: Sphingosine-1-phosphate receptor 1 (400 ×); F: Transforming growth factor-β1 (400 ×).

    Article Snippet: Xiaozhiling injection (Beijing China Resources High-Tech Natural Medicine Co., Ltd.); inhaled isoflurane (Baxter Healthcare Corporation, China); 4% neutral formaldehyde fixative solution; 6% croton oil (Beijing Huawei Ruike Chemical Co., Ltd.); pyridine (Beijing Lambolide Trading Co., Ltd.); ether (Xilong Science Co., Ltd.); horseradish peroxidase-conjugated polyclonal anti-rabbit/mouse IgG (Boster); an anti-TGF-β1 rabbit polyclonal antibody (Proteintech); an anti-Sphk1 rabbit polyclonal antibody (Proteintech); an anti-sphingosine-1-phosphate receptor 1 (S1PR1) rabbit polyclonal antibody (Proteintech); and an alpha smooth muscle actin specific monoclonal antibody (Proteintech) were used in this study.

    Techniques: Immunohistochemical staining, Staining

    Expression of sphingosine kinase 1-sphingosine-1-phosphate pathway related proteins in rectal tissues. Sphk1: Sphingosine kinase 1; S1PR1: Sphingosine-1-phosphate receptor 1; TGF-β1: Transforming growth factor-β1.

    Journal: World Journal of Gastrointestinal Surgery

    Article Title: Single-nucleus RNA sequencing and spatial transcriptomics reveal the mechanism by which Xiaozhiling injection treats internal hemorrhoids

    doi: 10.4240/wjgs.v17.i4.103494

    Figure Lengend Snippet: Expression of sphingosine kinase 1-sphingosine-1-phosphate pathway related proteins in rectal tissues. Sphk1: Sphingosine kinase 1; S1PR1: Sphingosine-1-phosphate receptor 1; TGF-β1: Transforming growth factor-β1.

    Article Snippet: Xiaozhiling injection (Beijing China Resources High-Tech Natural Medicine Co., Ltd.); inhaled isoflurane (Baxter Healthcare Corporation, China); 4% neutral formaldehyde fixative solution; 6% croton oil (Beijing Huawei Ruike Chemical Co., Ltd.); pyridine (Beijing Lambolide Trading Co., Ltd.); ether (Xilong Science Co., Ltd.); horseradish peroxidase-conjugated polyclonal anti-rabbit/mouse IgG (Boster); an anti-TGF-β1 rabbit polyclonal antibody (Proteintech); an anti-Sphk1 rabbit polyclonal antibody (Proteintech); an anti-sphingosine-1-phosphate receptor 1 (S1PR1) rabbit polyclonal antibody (Proteintech); and an alpha smooth muscle actin specific monoclonal antibody (Proteintech) were used in this study.

    Techniques: Expressing

    F4/80, F4/80 stain; PAI-1, plasminogen activator inhibitor-1 stain; PAS, periodic acid-Schiff stain; STZ, streptozotocin; TGF-β1, transforming growth factor beta-1 stain. Original magnification, ×400.

    Journal: Kidney Research and Clinical Practice

    Article Title: Pan-Nox inhibitor treatment improves renal function in aging murine diabetic kidneys

    doi: 10.23876/j.krcp.23.004

    Figure Lengend Snippet: F4/80, F4/80 stain; PAI-1, plasminogen activator inhibitor-1 stain; PAS, periodic acid-Schiff stain; STZ, streptozotocin; TGF-β1, transforming growth factor beta-1 stain. Original magnification, ×400.

    Article Snippet: Proteins were transferred onto a polyvinylidene difluoride membrane, and the membrane was hybridized in blocking buffer overnight at 4 °C with rabbit polyclonal anti-Nox1 antibody (1:1,000; Abcam Plc), rabbit polyclonal anti-Nox2 antibody (1:1,000; Bioworld Technology), rabbit polyclonal anti-Nox4 antibody (1:1,000; Bioworld Technology), rabbit polyclonal anti-PAI-1 antibody (1:1,000; Santa Cruz Biotechnology), mouse monoclonal anti-monocyte chemoattractant protein (MCP)-1 antibody (1:1000; Lsbio), rabbit polyclonal anti-type IV collagen antibody (1:1,000; Abcam Plc), rabbit polyclonal anti-TGF-β1 antibody (1:1,000; Abbkine), goat polyclonal anti-Klotho antibody (1:1,000; R&D Systems Inc.), rabbit polyclonal anti-phospho FoxO1 antibody (1:1,000; Lsbio), rabbit polyclonal anti-total-FoxO1 antibody (1:1,000; Cell Signaling Technology), rabbit polyclonal anti-NRF2 antibody (1:1,000; Cell Signaling Technology), or mouse monoclonal anti-β actin antibody (1:5,000; Sigma-Aldrich).

    Techniques: Staining

    (A) Mesangial expansion score, (B) scoring for F4/80-positive cells, (C) IHC staining score for plasminogen activator inhibitor 1 (PAI-1), and (D) IHC staining score for transforming growth factor beta 1 (TGF-β1). Data are shown as the mean ± standard error of mean. p < 0.001 vs. control or APX-115, # p < 0.05, ## p < 0.01, ### p < 0.001 vs. streptozotocin (STZ).

    Journal: Kidney Research and Clinical Practice

    Article Title: Pan-Nox inhibitor treatment improves renal function in aging murine diabetic kidneys

    doi: 10.23876/j.krcp.23.004

    Figure Lengend Snippet: (A) Mesangial expansion score, (B) scoring for F4/80-positive cells, (C) IHC staining score for plasminogen activator inhibitor 1 (PAI-1), and (D) IHC staining score for transforming growth factor beta 1 (TGF-β1). Data are shown as the mean ± standard error of mean. p < 0.001 vs. control or APX-115, # p < 0.05, ## p < 0.01, ### p < 0.001 vs. streptozotocin (STZ).

    Article Snippet: Proteins were transferred onto a polyvinylidene difluoride membrane, and the membrane was hybridized in blocking buffer overnight at 4 °C with rabbit polyclonal anti-Nox1 antibody (1:1,000; Abcam Plc), rabbit polyclonal anti-Nox2 antibody (1:1,000; Bioworld Technology), rabbit polyclonal anti-Nox4 antibody (1:1,000; Bioworld Technology), rabbit polyclonal anti-PAI-1 antibody (1:1,000; Santa Cruz Biotechnology), mouse monoclonal anti-monocyte chemoattractant protein (MCP)-1 antibody (1:1000; Lsbio), rabbit polyclonal anti-type IV collagen antibody (1:1,000; Abcam Plc), rabbit polyclonal anti-TGF-β1 antibody (1:1,000; Abbkine), goat polyclonal anti-Klotho antibody (1:1,000; R&D Systems Inc.), rabbit polyclonal anti-phospho FoxO1 antibody (1:1,000; Lsbio), rabbit polyclonal anti-total-FoxO1 antibody (1:1,000; Cell Signaling Technology), rabbit polyclonal anti-NRF2 antibody (1:1,000; Cell Signaling Technology), or mouse monoclonal anti-β actin antibody (1:5,000; Sigma-Aldrich).

    Techniques: Immunohistochemistry, Control

    (A) Representative immunoblots for transforming growth factor beta 1 (TGF-β1) and monocyte chemoattractant protein 1 (MCP-1); (B) densitometric analysis of immunoblots for TGF-β1 and MCP-1; (C) representative immunoblots for Nox1, Nox2, and Nox4; and (D) densitometric analysis of immunoblots for Nox1, Nox2, and Nox4. Data are shown as the mean ± standard error of mean. Nox, nicotinamide adenine dinucleotide phosphate oxidase; STX, streptozotocin. * p < 0.05, ** p < 0.01 vs. control or APX-115, # p < 0.05, ## p < 0.01 vs. STZ.

    Journal: Kidney Research and Clinical Practice

    Article Title: Pan-Nox inhibitor treatment improves renal function in aging murine diabetic kidneys

    doi: 10.23876/j.krcp.23.004

    Figure Lengend Snippet: (A) Representative immunoblots for transforming growth factor beta 1 (TGF-β1) and monocyte chemoattractant protein 1 (MCP-1); (B) densitometric analysis of immunoblots for TGF-β1 and MCP-1; (C) representative immunoblots for Nox1, Nox2, and Nox4; and (D) densitometric analysis of immunoblots for Nox1, Nox2, and Nox4. Data are shown as the mean ± standard error of mean. Nox, nicotinamide adenine dinucleotide phosphate oxidase; STX, streptozotocin. * p < 0.05, ** p < 0.01 vs. control or APX-115, # p < 0.05, ## p < 0.01 vs. STZ.

    Article Snippet: Proteins were transferred onto a polyvinylidene difluoride membrane, and the membrane was hybridized in blocking buffer overnight at 4 °C with rabbit polyclonal anti-Nox1 antibody (1:1,000; Abcam Plc), rabbit polyclonal anti-Nox2 antibody (1:1,000; Bioworld Technology), rabbit polyclonal anti-Nox4 antibody (1:1,000; Bioworld Technology), rabbit polyclonal anti-PAI-1 antibody (1:1,000; Santa Cruz Biotechnology), mouse monoclonal anti-monocyte chemoattractant protein (MCP)-1 antibody (1:1000; Lsbio), rabbit polyclonal anti-type IV collagen antibody (1:1,000; Abcam Plc), rabbit polyclonal anti-TGF-β1 antibody (1:1,000; Abbkine), goat polyclonal anti-Klotho antibody (1:1,000; R&D Systems Inc.), rabbit polyclonal anti-phospho FoxO1 antibody (1:1,000; Lsbio), rabbit polyclonal anti-total-FoxO1 antibody (1:1,000; Cell Signaling Technology), rabbit polyclonal anti-NRF2 antibody (1:1,000; Cell Signaling Technology), or mouse monoclonal anti-β actin antibody (1:5,000; Sigma-Aldrich).

    Techniques: Western Blot, Control