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upa inhibitor  (MedChemExpress)


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    Structured Review

    MedChemExpress upa inhibitor
    Upa Inhibitor, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/upa inhibitor/product/MedChemExpress
    Average 93 stars, based on 2 article reviews
    upa inhibitor - by Bioz Stars, 2026-02
    93/100 stars

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    Santa Cruz Biotechnology upa selective inhibitor uk122
    Figure 5. Effect of uPA inhibitor on DSS-induced colitis in C57BL/6 J mice. (A) Male mice were administered 2% DSS in their drinking water for 1 week, and intraperitoneally injected with 2 mg/kg or 4 mg/kg <t>UK122</t> or vehicle from day 1 to day 7 (n = 18 per group). They were sacrificed at day 8. (B) Representative macroscopic images of the colon in each group. The lower right panel represents a colorectum of mice that did not receive DSS. (C) DAI was evaluated at day 8 by the scoring method of Cooper et al.10 (D) Representative H&E staining images of colon sections in each group. The lower right panel represents a colorectum of mice that did not receive DSS. Scale bar, 100 μm. (E) Histologic score of H&E staining image was evaluated by the scoring method of Williams et al.11 Data represent mean ± SEM. *p < 0.05, **p < 0.01 by Dunnett’s multiple comparison test.
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    American Diagnostica upa stop-upa inhibitor
    Inhibition of <t>uPA</t> activity does not <t>prevent</t> <t>LPA-induced</t> E-cadherin junction disruption. OVCA429 cells were treated with or without LPA (30 μ M), as indicated, for 18 hours in the presence or absence of the uPA inhibitor designated uPA Stop (2.5 μ M), as indicated and processed for immunofluorescence staining for E-cadherin using anti-E-cadherin ectodomain antibody (1 : 300) and Alexa Fluor 488-conjugated secondary antibody (1 : 500; green). Blue-DAPI-stained nuclei.
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    Innovative Research Inc human urokinase type plasminogen activator upa
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    Human milk’s plasmin system is composed of plasminogen (zymogen), plasmin (the active enzyme), urokinase-type plasminogen activator (uPA), and tissue-type plasminogen activator (tPA) (plasminogen activators), and human plasminogen activator inhibitor type 1 (PAI-1) (plasminogen activator inhibitor). Plasminogen (the inactive zymogen) must be cleaved by uPA or tPA to become the active plasmin. The PAI-1 in human milk can block the activators’ (both tPA and uPA) conversion of plasminogen to active plasmin.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: Human milk’s plasmin system is composed of plasminogen (zymogen), plasmin (the active enzyme), urokinase-type plasminogen activator (uPA), and tissue-type plasminogen activator (tPA) (plasminogen activators), and human plasminogen activator inhibitor type 1 (PAI-1) (plasminogen activator inhibitor). Plasminogen (the inactive zymogen) must be cleaved by uPA or tPA to become the active plasmin. The PAI-1 in human milk can block the activators’ (both tPA and uPA) conversion of plasminogen to active plasmin.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Blocking Assay

    Measurements for the plasmin system in human milk from all lactating women in the study.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: Measurements for the plasmin system in human milk from all lactating women in the study.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Activity Assay

    The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across postnatal age at sampling. (A) Plasmin activity across postnatal age; (B) human urokinase-type plasminogen activator (uPA) across postnatal age; (C) human tissue-type plasminogen activator (tPA) across postnatal age; (D) human plasminogen activator inhibitor type 1 (PAI-1) across postnatal age in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across postnatal age at sampling. (A) Plasmin activity across postnatal age; (B) human urokinase-type plasminogen activator (uPA) across postnatal age; (C) human tissue-type plasminogen activator (tPA) across postnatal age; (D) human plasminogen activator inhibitor type 1 (PAI-1) across postnatal age in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Sampling, Activity Assay

    The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across gestational age (GA) at birth. (A) Plasmin activity across GA; (B) human urokinase-type plasminogen activator (uPA) across GA; (C) human tissue-type plasminogen activator (tPA) across GA; (D) human plasminogen activator inhibitor type 1 (PAI-1) across GA in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across gestational age (GA) at birth. (A) Plasmin activity across GA; (B) human urokinase-type plasminogen activator (uPA) across GA; (C) human tissue-type plasminogen activator (tPA) across GA; (D) human plasminogen activator inhibitor type 1 (PAI-1) across GA in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Activity Assay

    The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across postmenstrual age (PMA). (A) Plasmin activity across PMA; (B) human urokinase-type plasminogen activator (uPA) across PMA; (C) human tissue-type plasminogen activator (tPA) across PMA; (D) human plasminogen activator inhibitor type 1 (PAI-1) across PMA in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across postmenstrual age (PMA). (A) Plasmin activity across PMA; (B) human urokinase-type plasminogen activator (uPA) across PMA; (C) human tissue-type plasminogen activator (tPA) across PMA; (D) human plasminogen activator inhibitor type 1 (PAI-1) across PMA in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Activity Assay

    Figure 5. Effect of uPA inhibitor on DSS-induced colitis in C57BL/6 J mice. (A) Male mice were administered 2% DSS in their drinking water for 1 week, and intraperitoneally injected with 2 mg/kg or 4 mg/kg UK122 or vehicle from day 1 to day 7 (n = 18 per group). They were sacrificed at day 8. (B) Representative macroscopic images of the colon in each group. The lower right panel represents a colorectum of mice that did not receive DSS. (C) DAI was evaluated at day 8 by the scoring method of Cooper et al.10 (D) Representative H&E staining images of colon sections in each group. The lower right panel represents a colorectum of mice that did not receive DSS. Scale bar, 100 μm. (E) Histologic score of H&E staining image was evaluated by the scoring method of Williams et al.11 Data represent mean ± SEM. *p < 0.05, **p < 0.01 by Dunnett’s multiple comparison test.

    Journal: Scientific reports

    Article Title: Urokinase-type plasminogen activator blockade ameliorates experimental colitis in mice.

    doi: 10.1038/s41598-023-29824-1

    Figure Lengend Snippet: Figure 5. Effect of uPA inhibitor on DSS-induced colitis in C57BL/6 J mice. (A) Male mice were administered 2% DSS in their drinking water for 1 week, and intraperitoneally injected with 2 mg/kg or 4 mg/kg UK122 or vehicle from day 1 to day 7 (n = 18 per group). They were sacrificed at day 8. (B) Representative macroscopic images of the colon in each group. The lower right panel represents a colorectum of mice that did not receive DSS. (C) DAI was evaluated at day 8 by the scoring method of Cooper et al.10 (D) Representative H&E staining images of colon sections in each group. The lower right panel represents a colorectum of mice that did not receive DSS. Scale bar, 100 μm. (E) Histologic score of H&E staining image was evaluated by the scoring method of Williams et al.11 Data represent mean ± SEM. *p < 0.05, **p < 0.01 by Dunnett’s multiple comparison test.

    Article Snippet: The uPA-selective inhibitor UK122 (Santa Cruz Biotechnology, Dallas, TX) was dissolved in dimethyl sulfoxide (DMSO) and saline.

    Techniques: Injection, Staining, Comparison

    Figure 6. Cytokine expression in colorectal tissue from DSS-treated uPA−/− mice, and C57BL/6 J mice intraperitoneally injected with UK122. (A) Cytokine concentration in the colorectal extracts of WT (n = 8) and uPA−/− (n = 10) mice measured using Bio-Plex Pro Mouse Cytokine 23-Plex Assay kit in triplicate. (B) Cytokine concentration in the colorectal extracts of 8 mice treated with 2 mg/kg or 4 mg/kg UK122 or vehicle measured using Bio-Plex Pro Mouse Cytokine 23-Plex Assay kit in duplicate. Data represent mean ± SEM. *p < 0.05, by Student’s t test (A) and Dunnett’s multiple comparison test (B).

    Journal: Scientific reports

    Article Title: Urokinase-type plasminogen activator blockade ameliorates experimental colitis in mice.

    doi: 10.1038/s41598-023-29824-1

    Figure Lengend Snippet: Figure 6. Cytokine expression in colorectal tissue from DSS-treated uPA−/− mice, and C57BL/6 J mice intraperitoneally injected with UK122. (A) Cytokine concentration in the colorectal extracts of WT (n = 8) and uPA−/− (n = 10) mice measured using Bio-Plex Pro Mouse Cytokine 23-Plex Assay kit in triplicate. (B) Cytokine concentration in the colorectal extracts of 8 mice treated with 2 mg/kg or 4 mg/kg UK122 or vehicle measured using Bio-Plex Pro Mouse Cytokine 23-Plex Assay kit in duplicate. Data represent mean ± SEM. *p < 0.05, by Student’s t test (A) and Dunnett’s multiple comparison test (B).

    Article Snippet: The uPA-selective inhibitor UK122 (Santa Cruz Biotechnology, Dallas, TX) was dissolved in dimethyl sulfoxide (DMSO) and saline.

    Techniques: Expressing, Injection, Concentration Assay, Plex Assay, Comparison

    Inhibition of uPA activity does not prevent LPA-induced E-cadherin junction disruption. OVCA429 cells were treated with or without LPA (30 μ M), as indicated, for 18 hours in the presence or absence of the uPA inhibitor designated uPA Stop (2.5 μ M), as indicated and processed for immunofluorescence staining for E-cadherin using anti-E-cadherin ectodomain antibody (1 : 300) and Alexa Fluor 488-conjugated secondary antibody (1 : 500; green). Blue-DAPI-stained nuclei.

    Journal: Journal of Oncology

    Article Title: Lysophosphatidic Acid Disrupts Junctional Integrity and Epithelial Cohesion in Ovarian Cancer Cells

    doi: 10.1155/2012/501492

    Figure Lengend Snippet: Inhibition of uPA activity does not prevent LPA-induced E-cadherin junction disruption. OVCA429 cells were treated with or without LPA (30 μ M), as indicated, for 18 hours in the presence or absence of the uPA inhibitor designated uPA Stop (2.5 μ M), as indicated and processed for immunofluorescence staining for E-cadherin using anti-E-cadherin ectodomain antibody (1 : 300) and Alexa Fluor 488-conjugated secondary antibody (1 : 500; green). Blue-DAPI-stained nuclei.

    Article Snippet: In some experiments, cells were pretreated prior to addition of LPA with inhibitor (or equivalent concentrations of DMSO) for 1.5 to 3 hours (GM6001-MMP inhibitor, Chemicon, 25 μ M; Ki16425-LPA receptor inhibitor, Cayman Chemical, 40 μ M; uPA Stop-uPA inhibitor, American Diagnostica, 2.5 μ M).

    Techniques: Inhibition, Activity Assay, Immunofluorescence, Staining

    Human milk’s plasmin system is composed of plasminogen (zymogen), plasmin (the active enzyme), urokinase-type plasminogen activator (uPA), and tissue-type plasminogen activator (tPA) (plasminogen activators), and human plasminogen activator inhibitor type 1 (PAI-1) (plasminogen activator inhibitor). Plasminogen (the inactive zymogen) must be cleaved by uPA or tPA to become the active plasmin. The PAI-1 in human milk can block the activators’ (both tPA and uPA) conversion of plasminogen to active plasmin.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: Human milk’s plasmin system is composed of plasminogen (zymogen), plasmin (the active enzyme), urokinase-type plasminogen activator (uPA), and tissue-type plasminogen activator (tPA) (plasminogen activators), and human plasminogen activator inhibitor type 1 (PAI-1) (plasminogen activator inhibitor). Plasminogen (the inactive zymogen) must be cleaved by uPA or tPA to become the active plasmin. The PAI-1 in human milk can block the activators’ (both tPA and uPA) conversion of plasminogen to active plasmin.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Blocking Assay

    Measurements for the plasmin system in human milk from all lactating women in the study.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: Measurements for the plasmin system in human milk from all lactating women in the study.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Activity Assay

    The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across postnatal age at sampling. (A) Plasmin activity across postnatal age; (B) human urokinase-type plasminogen activator (uPA) across postnatal age; (C) human tissue-type plasminogen activator (tPA) across postnatal age; (D) human plasminogen activator inhibitor type 1 (PAI-1) across postnatal age in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across postnatal age at sampling. (A) Plasmin activity across postnatal age; (B) human urokinase-type plasminogen activator (uPA) across postnatal age; (C) human tissue-type plasminogen activator (tPA) across postnatal age; (D) human plasminogen activator inhibitor type 1 (PAI-1) across postnatal age in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Sampling, Activity Assay

    The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across gestational age (GA) at birth. (A) Plasmin activity across GA; (B) human urokinase-type plasminogen activator (uPA) across GA; (C) human tissue-type plasminogen activator (tPA) across GA; (D) human plasminogen activator inhibitor type 1 (PAI-1) across GA in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across gestational age (GA) at birth. (A) Plasmin activity across GA; (B) human urokinase-type plasminogen activator (uPA) across GA; (C) human tissue-type plasminogen activator (tPA) across GA; (D) human plasminogen activator inhibitor type 1 (PAI-1) across GA in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Activity Assay

    The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across postmenstrual age (PMA). (A) Plasmin activity across PMA; (B) human urokinase-type plasminogen activator (uPA) across PMA; (C) human tissue-type plasminogen activator (tPA) across PMA; (D) human plasminogen activator inhibitor type 1 (PAI-1) across PMA in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Journal: Frontiers in Pediatrics

    Article Title: Premature delivery impacts the concentration of plasminogen activators and a plasminogen activator inhibitor and the plasmin activity in human milk

    doi: 10.3389/fped.2022.917179

    Figure Lengend Snippet: The levels of plasmin system components in milk from extremely preterm-(EP), very preterm-(VP), and term-delivering mothers across postmenstrual age (PMA). (A) Plasmin activity across PMA; (B) human urokinase-type plasminogen activator (uPA) across PMA; (C) human tissue-type plasminogen activator (tPA) across PMA; (D) human plasminogen activator inhibitor type 1 (PAI-1) across PMA in human milk from EP ( n = 20), VP ( n = 12), term groups ( n = 8), and combined groups (overall, n = 40). r , Spearman correlation.

    Article Snippet: The concentrations of human urokinase-type plasminogen activator (uPA), human tissue-type plasminogen activator (tPA), human plasminogen activator inhibitor type 1 (PAI-1), human PAI-1/uPA complex and PAI-1/tPA complex were determined using ELISA kits (IHUPAKT, IHTPAKT, IHPAIKT, IHPAIUPAKT-COM, and HPAITPAKT-COM, Innovative Research, Inc.) according to the protocols described by the manufacturer.

    Techniques: Activity Assay