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antibodies against timp1  (Proteintech)


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    Structured Review

    Proteintech antibodies against timp1
    Antibodies Against Timp1, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 49 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/antibodies against timp1/product/Proteintech
    Average 95 stars, based on 49 article reviews
    antibodies against timp1 - by Bioz Stars, 2026-02
    95/100 stars

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    Proteintech anti timp1 antibodies
    <t>TIMP1</t> expression in several types of cancer. (A) UALCAN database was used to analyze the expression levels of TIMP1 in several types of pan-cancer tissues (indicated by the red box) and their corresponding normal tissues (indicated by the blue box). (B) Expression of TIMP1 was significantly upregulated in colon cancer tissues compared with that in normal tissues. (C) Expression level of TIMP1 was significantly upregulated in colon tissues compared with that in normal tissues, based on TCGA data from the Gene Expression Profiling Interactive Analysis 2.0 database. (D) Expression level of TIMP1 was significantly upregulated in colon tissues (G2) compared with in normal tissues (G1) in the GSE24550 dataset. (E) Protein expression of TIMP1 in colon tissues from CPTAC data based on the UALCAN database. *P<0.05; ****P<0.0001. TIMP1, tissue inhibitor of matrix metalloproteinase 1; UALCAN, University of Alabama at Birmingham CANcer data analysis Portal; TCGA, The Cancer Genome Atlas; CPTAC, Clinical Proteomic Tumor Analysis Consortium; TPM, transcripts per million; G, grade; COAD, colon adenocarcinoma.
    Anti Timp1 Antibodies, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Proteintech timp1
    Myeloid-specific Nogo-B deficiency alleviates liver injury and fibrosis. ( A ) Breeding scheme used to generate mice with myeloid-specific Nogo-B deletion. ( B ) Identification of myeloid-specific Nogo-B-deficient mice. ( C ) Serum Nogo-B concentrations in the 3 liver fibrosis models, as determined by ELISA. ( D ) Measurement of ALT and AST in the serum of the mice. ( E ) Collagen I and α-SMA mRNA expression in the murine livers was evaluated through qRT-PCR. ( F–H ) Liver sections from the mice were subjected to H&E and Sirius Red staining and Masson staining and α-SMA IHC analysis, and the proportions of Sirius red-positive and Masson-positive and a-SMA-positive regions were quantified. ( I–K ) Hepatic protein levels of collagen I, MMP-9, α-SMA, and <t>TIMP-1</t> were assessed via Western blotting; GAPDH served as the loading control. The data are presented as the means ± SEMs; n = 6 per group; original magnification, 10×; scale bars, 200 μm; ∗∗ P < .01.
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    Proteintech metalloproteinase 1 timp1 rabbit pab
    Western blot analysis of EECs treated with Tellimagrandin II: ( a ) protein immunoblot; ( b ) ALDH7A1; ( c ) SMOX; ( d ) NLRP3; ( e ) Caspase-1; ( f ) β-catenin; ( g ) cleaved Caspase-3; ( h ) BAX; ( i ) MMP2; ( j ) <t>TIMP1.</t> Each experiment was repeated three times. *:P <0.05; **:P <0.01; ***:P <0.001; ****P <0.0001.
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    Proteintech timp1 elisa kit
    Western blot analysis of EECs treated with Tellimagrandin II: ( a ) protein immunoblot; ( b ) ALDH7A1; ( c ) SMOX; ( d ) NLRP3; ( e ) Caspase-1; ( f ) β-catenin; ( g ) cleaved Caspase-3; ( h ) BAX; ( i ) MMP2; ( j ) <t>TIMP1.</t> Each experiment was repeated three times. *:P <0.05; **:P <0.01; ***:P <0.001; ****P <0.0001.
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    Proteintech timp1 concentrations
    Western blot analysis of EECs treated with Tellimagrandin II: ( a ) protein immunoblot; ( b ) ALDH7A1; ( c ) SMOX; ( d ) NLRP3; ( e ) Caspase-1; ( f ) β-catenin; ( g ) cleaved Caspase-3; ( h ) BAX; ( i ) MMP2; ( j ) <t>TIMP1.</t> Each experiment was repeated three times. *:P <0.05; **:P <0.01; ***:P <0.001; ****P <0.0001.
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    Image Search Results


    TIMP1 expression in several types of cancer. (A) UALCAN database was used to analyze the expression levels of TIMP1 in several types of pan-cancer tissues (indicated by the red box) and their corresponding normal tissues (indicated by the blue box). (B) Expression of TIMP1 was significantly upregulated in colon cancer tissues compared with that in normal tissues. (C) Expression level of TIMP1 was significantly upregulated in colon tissues compared with that in normal tissues, based on TCGA data from the Gene Expression Profiling Interactive Analysis 2.0 database. (D) Expression level of TIMP1 was significantly upregulated in colon tissues (G2) compared with in normal tissues (G1) in the GSE24550 dataset. (E) Protein expression of TIMP1 in colon tissues from CPTAC data based on the UALCAN database. *P<0.05; ****P<0.0001. TIMP1, tissue inhibitor of matrix metalloproteinase 1; UALCAN, University of Alabama at Birmingham CANcer data analysis Portal; TCGA, The Cancer Genome Atlas; CPTAC, Clinical Proteomic Tumor Analysis Consortium; TPM, transcripts per million; G, grade; COAD, colon adenocarcinoma.

    Journal: Oncology Letters

    Article Title: TIMP1 expression in colorectal cancer: Linking prognosis, tumor immunity and molecular pathways

    doi: 10.3892/ol.2025.15390

    Figure Lengend Snippet: TIMP1 expression in several types of cancer. (A) UALCAN database was used to analyze the expression levels of TIMP1 in several types of pan-cancer tissues (indicated by the red box) and their corresponding normal tissues (indicated by the blue box). (B) Expression of TIMP1 was significantly upregulated in colon cancer tissues compared with that in normal tissues. (C) Expression level of TIMP1 was significantly upregulated in colon tissues compared with that in normal tissues, based on TCGA data from the Gene Expression Profiling Interactive Analysis 2.0 database. (D) Expression level of TIMP1 was significantly upregulated in colon tissues (G2) compared with in normal tissues (G1) in the GSE24550 dataset. (E) Protein expression of TIMP1 in colon tissues from CPTAC data based on the UALCAN database. *P<0.05; ****P<0.0001. TIMP1, tissue inhibitor of matrix metalloproteinase 1; UALCAN, University of Alabama at Birmingham CANcer data analysis Portal; TCGA, The Cancer Genome Atlas; CPTAC, Clinical Proteomic Tumor Analysis Consortium; TPM, transcripts per million; G, grade; COAD, colon adenocarcinoma.

    Article Snippet: The sections were then incubated with anti-TIMP1 antibodies (1:300 dilution; cat. no. 16644-1-AP; Proteintech Group, Inc.) overnight at 4°C, succeeded by incubation with a biotinylated goat anti-rabbit secondary antibody working solution (1:500 dilution; cat. no. SA1020; Boster Biological Technology Co. Ltd.) at 37°C for 30 min. Immunodetection was subsequently executed employing the Dako EnVision detection system (Agilent Technologies, Inc.).

    Techniques: Expressing, Gene Expression

    Association between TIMP1 expression and survival prognosis of patients with CRC. (A) Association between TIMP1 expression and the overall survival of patients with CRC was analyzed using the GEPIA 2.0 database. (B) Association between TIMP1 expression and the overall survival of patients with colon cancer was analyzed using the University of Alabama at Birmingham CANcer data analysis Portal database. (C) Kaplan-Meier survival curve for TIMP1 in CRC-The Cancer Genome Atlas data, with different groups compared using the log-rank test. (D) Association between TIMP1 expression and the disease-free survival of patients with CRC was analyzed using the GEPIA 2.0 database. TIMP1, tissue inhibitor of matrix metalloproteinase 1; CRC, colorectal cancer; GEPIA, Gene Expression Profiling Interactive Analysis; HR, hazard ratio; CI, confidence interval; COAD, colon adenocarcinoma.

    Journal: Oncology Letters

    Article Title: TIMP1 expression in colorectal cancer: Linking prognosis, tumor immunity and molecular pathways

    doi: 10.3892/ol.2025.15390

    Figure Lengend Snippet: Association between TIMP1 expression and survival prognosis of patients with CRC. (A) Association between TIMP1 expression and the overall survival of patients with CRC was analyzed using the GEPIA 2.0 database. (B) Association between TIMP1 expression and the overall survival of patients with colon cancer was analyzed using the University of Alabama at Birmingham CANcer data analysis Portal database. (C) Kaplan-Meier survival curve for TIMP1 in CRC-The Cancer Genome Atlas data, with different groups compared using the log-rank test. (D) Association between TIMP1 expression and the disease-free survival of patients with CRC was analyzed using the GEPIA 2.0 database. TIMP1, tissue inhibitor of matrix metalloproteinase 1; CRC, colorectal cancer; GEPIA, Gene Expression Profiling Interactive Analysis; HR, hazard ratio; CI, confidence interval; COAD, colon adenocarcinoma.

    Article Snippet: The sections were then incubated with anti-TIMP1 antibodies (1:300 dilution; cat. no. 16644-1-AP; Proteintech Group, Inc.) overnight at 4°C, succeeded by incubation with a biotinylated goat anti-rabbit secondary antibody working solution (1:500 dilution; cat. no. SA1020; Boster Biological Technology Co. Ltd.) at 37°C for 30 min. Immunodetection was subsequently executed employing the Dako EnVision detection system (Agilent Technologies, Inc.).

    Techniques: Expressing, Gene Expression

    TIMP1 serves as a prognostic factor for overall survival in CRC. (A) Univariate and (B) multivariate Cox analyses of TCGA data of patients with CRC for TIMP1 expression and clinical characteristics. (C) Nomogram formulated to predict 1-year overall survival for patients with CRC from TCGA data. (D) Calibration curve for the overall survival nomogram model in the discovery cohort, where the diagonal dashed line denotes the ideal nomogram, and the red line represent the observed 1-year nomograms. TIMP1, tissue inhibitor of matrix metalloproteinase 1; CRC, colorectal cancer; TCGA, The Cancer Genome Atlas; HR, hazard ratio; CI, confidence interval; p, pathological; T, tumor; N, node; M, metastasis.

    Journal: Oncology Letters

    Article Title: TIMP1 expression in colorectal cancer: Linking prognosis, tumor immunity and molecular pathways

    doi: 10.3892/ol.2025.15390

    Figure Lengend Snippet: TIMP1 serves as a prognostic factor for overall survival in CRC. (A) Univariate and (B) multivariate Cox analyses of TCGA data of patients with CRC for TIMP1 expression and clinical characteristics. (C) Nomogram formulated to predict 1-year overall survival for patients with CRC from TCGA data. (D) Calibration curve for the overall survival nomogram model in the discovery cohort, where the diagonal dashed line denotes the ideal nomogram, and the red line represent the observed 1-year nomograms. TIMP1, tissue inhibitor of matrix metalloproteinase 1; CRC, colorectal cancer; TCGA, The Cancer Genome Atlas; HR, hazard ratio; CI, confidence interval; p, pathological; T, tumor; N, node; M, metastasis.

    Article Snippet: The sections were then incubated with anti-TIMP1 antibodies (1:300 dilution; cat. no. 16644-1-AP; Proteintech Group, Inc.) overnight at 4°C, succeeded by incubation with a biotinylated goat anti-rabbit secondary antibody working solution (1:500 dilution; cat. no. SA1020; Boster Biological Technology Co. Ltd.) at 37°C for 30 min. Immunodetection was subsequently executed employing the Dako EnVision detection system (Agilent Technologies, Inc.).

    Techniques: Expressing

    Association between TIMP1 expression and immunity in CRC. Heatmap illustrates the correlation analysis of TIMP1 expression with (A) TIMER and (B) EPIC scores. Red signifies a positive correlation, whilst blue indicates a negative correlation. The intensity of the red or blue color reflects the strength of the correlation, and the size of the circle indicates the magnitude of the correlation. In the schematic, a red line denotes a negative correlation between model scores/gene expression and immune scores, whereas a green line denotes a positive correlation. (C) Spearman's correlation analysis of TIMP1 expression with CD4 + and CD8 + T cells in CRC from The Cancer Genome Atlas database. (D) Spearman's correlation analysis of TIMP1 expression with TMB/MSI score distribution is shown. TIMP1, tissue inhibitor of matrix metalloproteinase 1; CRC, colorectal cancer; TMB, tumor mutation burden; MSI,/microsatellite instability; NK, natural killer.

    Journal: Oncology Letters

    Article Title: TIMP1 expression in colorectal cancer: Linking prognosis, tumor immunity and molecular pathways

    doi: 10.3892/ol.2025.15390

    Figure Lengend Snippet: Association between TIMP1 expression and immunity in CRC. Heatmap illustrates the correlation analysis of TIMP1 expression with (A) TIMER and (B) EPIC scores. Red signifies a positive correlation, whilst blue indicates a negative correlation. The intensity of the red or blue color reflects the strength of the correlation, and the size of the circle indicates the magnitude of the correlation. In the schematic, a red line denotes a negative correlation between model scores/gene expression and immune scores, whereas a green line denotes a positive correlation. (C) Spearman's correlation analysis of TIMP1 expression with CD4 + and CD8 + T cells in CRC from The Cancer Genome Atlas database. (D) Spearman's correlation analysis of TIMP1 expression with TMB/MSI score distribution is shown. TIMP1, tissue inhibitor of matrix metalloproteinase 1; CRC, colorectal cancer; TMB, tumor mutation burden; MSI,/microsatellite instability; NK, natural killer.

    Article Snippet: The sections were then incubated with anti-TIMP1 antibodies (1:300 dilution; cat. no. 16644-1-AP; Proteintech Group, Inc.) overnight at 4°C, succeeded by incubation with a biotinylated goat anti-rabbit secondary antibody working solution (1:500 dilution; cat. no. SA1020; Boster Biological Technology Co. Ltd.) at 37°C for 30 min. Immunodetection was subsequently executed employing the Dako EnVision detection system (Agilent Technologies, Inc.).

    Techniques: Expressing, Gene Expression, Mutagenesis

    Correlation of TIMP1 and signaling pathways in CRC. Spearman's correlation analysis plots reveal the correlation between pathway scores and TIMP1 expression in CRC samples from The Cancer Genome Atlas database. TIMP1, tissue inhibitor of matrix metalloproteinase 1; CRC, colorectal cancer; TPM, transcripts per million; EMT, epithelial-mesenchymal transition; ECM, extracellular matrix.

    Journal: Oncology Letters

    Article Title: TIMP1 expression in colorectal cancer: Linking prognosis, tumor immunity and molecular pathways

    doi: 10.3892/ol.2025.15390

    Figure Lengend Snippet: Correlation of TIMP1 and signaling pathways in CRC. Spearman's correlation analysis plots reveal the correlation between pathway scores and TIMP1 expression in CRC samples from The Cancer Genome Atlas database. TIMP1, tissue inhibitor of matrix metalloproteinase 1; CRC, colorectal cancer; TPM, transcripts per million; EMT, epithelial-mesenchymal transition; ECM, extracellular matrix.

    Article Snippet: The sections were then incubated with anti-TIMP1 antibodies (1:300 dilution; cat. no. 16644-1-AP; Proteintech Group, Inc.) overnight at 4°C, succeeded by incubation with a biotinylated goat anti-rabbit secondary antibody working solution (1:500 dilution; cat. no. SA1020; Boster Biological Technology Co. Ltd.) at 37°C for 30 min. Immunodetection was subsequently executed employing the Dako EnVision detection system (Agilent Technologies, Inc.).

    Techniques: Protein-Protein interactions, Expressing

    TIMP1 protein expression in the colorectal cancer cohort in the present study. (A) Representative images of IHC analysis of TIMP1 protein expression of NAT (n=78) and CC (n=78) tissue sections. Scale bar, 100 µm. (B) TIMP1 protein expression based on their staining index in NAT and CC specimens. (C) Patients with CC with high TIMP1 expression (IHC score ≥4) had a significantly worse prognosis than patients with low TIMP1 expression (IHC score <4). ***P<0.001. TIMP1, tissue inhibitor of matrix metalloproteinase 1; IHC, immunohistochemistry; NAT, nonmalignant adjacent tissues; CC, colon cancer.

    Journal: Oncology Letters

    Article Title: TIMP1 expression in colorectal cancer: Linking prognosis, tumor immunity and molecular pathways

    doi: 10.3892/ol.2025.15390

    Figure Lengend Snippet: TIMP1 protein expression in the colorectal cancer cohort in the present study. (A) Representative images of IHC analysis of TIMP1 protein expression of NAT (n=78) and CC (n=78) tissue sections. Scale bar, 100 µm. (B) TIMP1 protein expression based on their staining index in NAT and CC specimens. (C) Patients with CC with high TIMP1 expression (IHC score ≥4) had a significantly worse prognosis than patients with low TIMP1 expression (IHC score <4). ***P<0.001. TIMP1, tissue inhibitor of matrix metalloproteinase 1; IHC, immunohistochemistry; NAT, nonmalignant adjacent tissues; CC, colon cancer.

    Article Snippet: The sections were then incubated with anti-TIMP1 antibodies (1:300 dilution; cat. no. 16644-1-AP; Proteintech Group, Inc.) overnight at 4°C, succeeded by incubation with a biotinylated goat anti-rabbit secondary antibody working solution (1:500 dilution; cat. no. SA1020; Boster Biological Technology Co. Ltd.) at 37°C for 30 min. Immunodetection was subsequently executed employing the Dako EnVision detection system (Agilent Technologies, Inc.).

    Techniques: Expressing, Staining, Immunohistochemistry

    Myeloid-specific Nogo-B deficiency alleviates liver injury and fibrosis. ( A ) Breeding scheme used to generate mice with myeloid-specific Nogo-B deletion. ( B ) Identification of myeloid-specific Nogo-B-deficient mice. ( C ) Serum Nogo-B concentrations in the 3 liver fibrosis models, as determined by ELISA. ( D ) Measurement of ALT and AST in the serum of the mice. ( E ) Collagen I and α-SMA mRNA expression in the murine livers was evaluated through qRT-PCR. ( F–H ) Liver sections from the mice were subjected to H&E and Sirius Red staining and Masson staining and α-SMA IHC analysis, and the proportions of Sirius red-positive and Masson-positive and a-SMA-positive regions were quantified. ( I–K ) Hepatic protein levels of collagen I, MMP-9, α-SMA, and TIMP-1 were assessed via Western blotting; GAPDH served as the loading control. The data are presented as the means ± SEMs; n = 6 per group; original magnification, 10×; scale bars, 200 μm; ∗∗ P < .01.

    Journal: Cellular and Molecular Gastroenterology and Hepatology

    Article Title: Macrophage Nogo-B Drives Liver Fibrosis

    doi: 10.1016/j.jcmgh.2025.101622

    Figure Lengend Snippet: Myeloid-specific Nogo-B deficiency alleviates liver injury and fibrosis. ( A ) Breeding scheme used to generate mice with myeloid-specific Nogo-B deletion. ( B ) Identification of myeloid-specific Nogo-B-deficient mice. ( C ) Serum Nogo-B concentrations in the 3 liver fibrosis models, as determined by ELISA. ( D ) Measurement of ALT and AST in the serum of the mice. ( E ) Collagen I and α-SMA mRNA expression in the murine livers was evaluated through qRT-PCR. ( F–H ) Liver sections from the mice were subjected to H&E and Sirius Red staining and Masson staining and α-SMA IHC analysis, and the proportions of Sirius red-positive and Masson-positive and a-SMA-positive regions were quantified. ( I–K ) Hepatic protein levels of collagen I, MMP-9, α-SMA, and TIMP-1 were assessed via Western blotting; GAPDH served as the loading control. The data are presented as the means ± SEMs; n = 6 per group; original magnification, 10×; scale bars, 200 μm; ∗∗ P < .01.

    Article Snippet: The membranes were probed with the following primary antibodies: Nogo-B (rabbit mAb, Thermo Fisher), USP14, p-RIPK3, and p-MLKL (rabbit mAbs, Abcam); α-SMA, collagen I, TIMP1, MMP9, caspase-1, cleaved caspase-1, pro-IL-1β, cleaved IL-1β, GAPDH, RIPK3, MLKL, CD11b, and LY6G (rabbit mAbs, Cell Signaling Technology); RIPK3 (mouse mAb, Cell Signaling Technology); USP14, NLRP3, and ASC (mouse mAbs, Proteintech); and Trim28 and Prpf19 (rabbit mAbs, Proteintech).

    Techniques: Enzyme-linked Immunosorbent Assay, Expressing, Quantitative RT-PCR, Staining, Western Blot, Control

    Western blot analysis of EECs treated with Tellimagrandin II: ( a ) protein immunoblot; ( b ) ALDH7A1; ( c ) SMOX; ( d ) NLRP3; ( e ) Caspase-1; ( f ) β-catenin; ( g ) cleaved Caspase-3; ( h ) BAX; ( i ) MMP2; ( j ) TIMP1. Each experiment was repeated three times. *:P <0.05; **:P <0.01; ***:P <0.001; ****P <0.0001.

    Journal: Journal of Inflammation Research

    Article Title: Tellimagrandin II Stimulates Inflammasomes by Causing an Accumulation of 3-Aminopropanal, Which Promotes Apoptosis of Endometriotic Cells While Inhibiting Invasion

    doi: 10.2147/JIR.S558146

    Figure Lengend Snippet: Western blot analysis of EECs treated with Tellimagrandin II: ( a ) protein immunoblot; ( b ) ALDH7A1; ( c ) SMOX; ( d ) NLRP3; ( e ) Caspase-1; ( f ) β-catenin; ( g ) cleaved Caspase-3; ( h ) BAX; ( i ) MMP2; ( j ) TIMP1. Each experiment was repeated three times. *:P <0.05; **:P <0.01; ***:P <0.001; ****P <0.0001.

    Article Snippet: Tellimagrandin II (Yongjian: B02179 ), Spermine Oxidase (SMOX) Polyclonal antibody (proteintech: 15052-1-AP), Aldehyde Dehydrogenase 7A1 (ALDH7A1) Polyclonal antibody (proteintech: 10368-1-AP), Anti-NLR Family, Pyrin Domain Containing Protein 3 (NLRP3) Rabbit pAb (Servicebio: GB114320-50), Recombinant Anti-beta Catenin (β-Catenin) antibody (Servicebio: GB150016-100), Anti-Matrix Metallopeptidase 2 (MMP2) Rabbit pAb (Servicebio: GB11130-100), Anti- Tissue Inhibitors of Metalloproteinase 1 (TIMP1) Rabbit pAb (proteintech: 16644-1-AP), Anti-Caspase-3 Rabbit pAb (Servicebio: GB115600-100), Anti-Bcl-2-associated X(Bax) Rabbit pAb (Servicebio: GB11690-100), Anti-Caspase-1 Rabbit pAb (Servicebio: GB11383-100), DMEM/F12 (Glutamine and HEPES)(M&C GENE: CM10092), Fetal Bovine Serum Gold (YEASEN: 40130ES76), penicillin streptomycin mixture (Servicebio: P1400), 1×PBS buffer (Solarbio: P1020), trypsin-EDTA digestion solution (Phenol Red)(Solarbio: T1320), CCK-8 kit (Sola rbio: CA1210), Annexin V-FITC Apoptosis detection kit (Beyotime: C1062S), 96-well cell culture plate (Servicebio:) CCP-96H, SWE matrix adhesive (Solarbio: G4131-5ML), crystal violet staining solution (Solarbio: G1014-50ML), paraformaldehyde fixative (Solarbio: G1101-500ML), Transwell chamber (Corning: WG3422) Cell culture flasks (Corning: 430639), 12Z EECs line (Bioharbor: LH-H337), DMSO (Servicebio: GC203006-10mL), Propidium Iodide (proteintech: CM18819), Flow cytometer (BD: FACSAria II), Gel imaging system (Alpha: 2200) Electrophoresis apparatus (Thermo: EC250-90), Thermo Corporation, USA; Pendulum type decolorizing shaker (model: DS-2S100), Nanodrop micro spectrophotometer (Illumina: Nanodrop2000), sequencing platform machine (Illumina: NovaSeq X Plus).

    Techniques: Western Blot