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94
Proteintech primary antibodies against plau
In vitro experiments confirming ellagic acid (EA) target on <t>PLAU</t> to regulate NF-κB signaling pathway in corneal endothelial cells. ( A – C ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 in H 2 O 2 -treated B4G12 cells, with or without EA treatment. The relative protein expression levels are shown for B PLAU and C the ratio of phospho-NF-κB p65 to NF-κB p65 ( n = 3 for PLAU, and n = 4 for phospho-NF-κB p65 to NF-κB p65). ( D – F ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 in UVA-irradiated B4G12 cells, with or without EA treatment. Relative protein expression levels are shown for E PLAU and F the ratio of phospho-NF-κB p65 to total NF-κB p65 ( n = 3). ( G – I ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 following siPLAU treatment in H 2 O 2 -treated B4G12 cells, with or without EA. Relative protein expression levels are presented for G PLAU and I the ratio of phospho-NF-κB p65 to NF-κB p65 ( n = 3 for PLAU, and n = 4 for phospho-NF-κB p65 to NF-κB p65). ( J ) Schematic diagram illustrating the proposed anti-inflammatory and anti-oxidant mechanisms of EA in FECD, highlighting its role in modulating the NF-κB pathway. All data are presented as mean ± SD. * P < 0.05, ** P < 0.01 by 1-way ANOVA with Tukey’s post hoc test.
Primary Antibodies Against Plau, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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primary antibodies against plau - by Bioz Stars, 2026-09
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ABclonal Biotechnology antibodies against fibronectin, claudin-1, upa, mt1-mmp, cleaved caspase-3, phospho-mtor, total mtor, and phospho-akt
In vitro experiments confirming ellagic acid (EA) target on <t>PLAU</t> to regulate NF-κB signaling pathway in corneal endothelial cells. ( A – C ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 in H 2 O 2 -treated B4G12 cells, with or without EA treatment. The relative protein expression levels are shown for B PLAU and C the ratio of phospho-NF-κB p65 to NF-κB p65 ( n = 3 for PLAU, and n = 4 for phospho-NF-κB p65 to NF-κB p65). ( D – F ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 in UVA-irradiated B4G12 cells, with or without EA treatment. Relative protein expression levels are shown for E PLAU and F the ratio of phospho-NF-κB p65 to total NF-κB p65 ( n = 3). ( G – I ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 following siPLAU treatment in H 2 O 2 -treated B4G12 cells, with or without EA. Relative protein expression levels are presented for G PLAU and I the ratio of phospho-NF-κB p65 to NF-κB p65 ( n = 3 for PLAU, and n = 4 for phospho-NF-κB p65 to NF-κB p65). ( J ) Schematic diagram illustrating the proposed anti-inflammatory and anti-oxidant mechanisms of EA in FECD, highlighting its role in modulating the NF-κB pathway. All data are presented as mean ± SD. * P < 0.05, ** P < 0.01 by 1-way ANOVA with Tukey’s post hoc test.
Antibodies Against Fibronectin, Claudin 1, Upa, Mt1 Mmp, Cleaved Caspase 3, Phospho Mtor, Total Mtor, And Phospho Akt, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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antibodies against fibronectin, claudin-1, upa, mt1-mmp, cleaved caspase-3, phospho-mtor, total mtor, and phospho-akt - by Bioz Stars, 2026-09
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Proteintech antibody against plau
Expression levels of <t>PLAU</t> protein in PDAC and paraneoplastic tissues. (A) Representative images of PLAU protein in PDAC and control tissues by IHC staining. Bars = 200 μm. (B) Quantitative results of PLAU protein in PDACs and controls, **** p < 0.0001. (C) Correlation between PLAU protein expression in PDAC and tumor differentiation status of patients, ** p < 0.01. (D) Correlation between PLAU protein expression in PDAC and lymph node metastatic status of patients, * p < 0.05.
Antibody Against Plau, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/antibody+against+upa/uPA%2FUrokinase+Antibody/pmc10014786-135-7-13
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Santa Cruz Biotechnology rabbit polyclonal antibody against upa
Expression levels of <t>PLAU</t> protein in PDAC and paraneoplastic tissues. (A) Representative images of PLAU protein in PDAC and control tissues by IHC staining. Bars = 200 μm. (B) Quantitative results of PLAU protein in PDACs and controls, **** p < 0.0001. (C) Correlation between PLAU protein expression in PDAC and tumor differentiation status of patients, ** p < 0.01. (D) Correlation between PLAU protein expression in PDAC and lymph node metastatic status of patients, * p < 0.05.
Rabbit Polyclonal Antibody Against Upa, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Gentex Corporation primary antibodies against urokinase-type plasminogen activator (upa)
Expression levels of <t>PLAU</t> protein in PDAC and paraneoplastic tissues. (A) Representative images of PLAU protein in PDAC and control tissues by IHC staining. Bars = 200 μm. (B) Quantitative results of PLAU protein in PDACs and controls, **** p < 0.0001. (C) Correlation between PLAU protein expression in PDAC and tumor differentiation status of patients, ** p < 0.01. (D) Correlation between PLAU protein expression in PDAC and lymph node metastatic status of patients, * p < 0.05.
Primary Antibodies Against Urokinase Type Plasminogen Activator (Upa), supplied by Gentex Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GeneTex primary antibodies against upar and upa gtx59605 and gtx89445
Expression levels of <t>PLAU</t> protein in PDAC and paraneoplastic tissues. (A) Representative images of PLAU protein in PDAC and control tissues by IHC staining. Bars = 200 μm. (B) Quantitative results of PLAU protein in PDACs and controls, **** p < 0.0001. (C) Correlation between PLAU protein expression in PDAC and tumor differentiation status of patients, ** p < 0.01. (D) Correlation between PLAU protein expression in PDAC and lymph node metastatic status of patients, * p < 0.05.
Primary Antibodies Against Upar And Upa Gtx59605 And Gtx89445, supplied by GeneTex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GeneTex primary antibodies against upa and upar
Expression levels of <t>PLAU</t> protein in PDAC and paraneoplastic tissues. (A) Representative images of PLAU protein in PDAC and control tissues by IHC staining. Bars = 200 μm. (B) Quantitative results of PLAU protein in PDACs and controls, **** p < 0.0001. (C) Correlation between PLAU protein expression in PDAC and tumor differentiation status of patients, ** p < 0.01. (D) Correlation between PLAU protein expression in PDAC and lymph node metastatic status of patients, * p < 0.05.
Primary Antibodies Against Upa And Upar, supplied by GeneTex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc rabbit antibodies against human mmp-2, mmp-9, upa, pi3k, and p -pi3k
Stellettin B regulated the expression levels in the <t>PI3K/AKT/mTOR</t> signaling pathway. Western blotting analysis was employed to analyze the expressions levels of p -FAK, p -PI3K, p -AKT, and p -mTOR in HA22T and HepG2 cells treated with Stellettin B. Zero refers to cells treated with DMSO vehicle as a control. β -Actin was used as the internal control.
Rabbit Antibodies Against Human Mmp 2, Mmp 9, Upa, Pi3k, And P Pi3k, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology primary antibodies against upa
Stellettin B regulated the expression levels in the <t>PI3K/AKT/mTOR</t> signaling pathway. Western blotting analysis was employed to analyze the expressions levels of p -FAK, p -PI3K, p -AKT, and p -mTOR in HA22T and HepG2 cells treated with Stellettin B. Zero refers to cells treated with DMSO vehicle as a control. β -Actin was used as the internal control.
Primary Antibodies Against Upa, supplied by Santa Cruz Biotechnology, 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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Image Search Results


In vitro experiments confirming ellagic acid (EA) target on PLAU to regulate NF-κB signaling pathway in corneal endothelial cells. ( A – C ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 in H 2 O 2 -treated B4G12 cells, with or without EA treatment. The relative protein expression levels are shown for B PLAU and C the ratio of phospho-NF-κB p65 to NF-κB p65 ( n = 3 for PLAU, and n = 4 for phospho-NF-κB p65 to NF-κB p65). ( D – F ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 in UVA-irradiated B4G12 cells, with or without EA treatment. Relative protein expression levels are shown for E PLAU and F the ratio of phospho-NF-κB p65 to total NF-κB p65 ( n = 3). ( G – I ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 following siPLAU treatment in H 2 O 2 -treated B4G12 cells, with or without EA. Relative protein expression levels are presented for G PLAU and I the ratio of phospho-NF-κB p65 to NF-κB p65 ( n = 3 for PLAU, and n = 4 for phospho-NF-κB p65 to NF-κB p65). ( J ) Schematic diagram illustrating the proposed anti-inflammatory and anti-oxidant mechanisms of EA in FECD, highlighting its role in modulating the NF-κB pathway. All data are presented as mean ± SD. * P < 0.05, ** P < 0.01 by 1-way ANOVA with Tukey’s post hoc test.

Journal: Investigative Ophthalmology & Visual Science

Article Title: Integrated Transcriptomics and Experimental Validation Reveal That Ellagic Acid Alleviates Fuchs Endothelial Corneal Dystrophy via PLAU/NF-κB Signaling

doi: 10.1167/iovs.67.1.31

Figure Lengend Snippet: In vitro experiments confirming ellagic acid (EA) target on PLAU to regulate NF-κB signaling pathway in corneal endothelial cells. ( A – C ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 in H 2 O 2 -treated B4G12 cells, with or without EA treatment. The relative protein expression levels are shown for B PLAU and C the ratio of phospho-NF-κB p65 to NF-κB p65 ( n = 3 for PLAU, and n = 4 for phospho-NF-κB p65 to NF-κB p65). ( D – F ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 in UVA-irradiated B4G12 cells, with or without EA treatment. Relative protein expression levels are shown for E PLAU and F the ratio of phospho-NF-κB p65 to total NF-κB p65 ( n = 3). ( G – I ) Western blot analysis of PLAU, NF-κB p65, and phospho-NF-κB p65 following siPLAU treatment in H 2 O 2 -treated B4G12 cells, with or without EA. Relative protein expression levels are presented for G PLAU and I the ratio of phospho-NF-κB p65 to NF-κB p65 ( n = 3 for PLAU, and n = 4 for phospho-NF-κB p65 to NF-κB p65). ( J ) Schematic diagram illustrating the proposed anti-inflammatory and anti-oxidant mechanisms of EA in FECD, highlighting its role in modulating the NF-κB pathway. All data are presented as mean ± SD. * P < 0.05, ** P < 0.01 by 1-way ANOVA with Tukey’s post hoc test.

Article Snippet: Primary antibodies against PLAU (Proteintech, China; #17968-1-AP), NF-κB p65 (Abcam, UK; #ab32536), phospho-NF-κB p65 (S536; Abcam, UK; #ab76302), GAPDH (ABclonal, China; #AC002), and β-Actin (ABclonal, China; #AC004) were applied overnight at 4°C.

Techniques: In Vitro, Western Blot, Expressing, Irradiation

Expression levels of PLAU protein in PDAC and paraneoplastic tissues. (A) Representative images of PLAU protein in PDAC and control tissues by IHC staining. Bars = 200 μm. (B) Quantitative results of PLAU protein in PDACs and controls, **** p < 0.0001. (C) Correlation between PLAU protein expression in PDAC and tumor differentiation status of patients, ** p < 0.01. (D) Correlation between PLAU protein expression in PDAC and lymph node metastatic status of patients, * p < 0.05.

Journal: Frontiers in Pharmacology

Article Title: Integrated analysis of Dendrobium nobile extract Dendrobin A against pancreatic ductal adenocarcinoma based on network pharmacology, bioinformatics, and validation experiments

doi: 10.3389/fphar.2023.1079539

Figure Lengend Snippet: Expression levels of PLAU protein in PDAC and paraneoplastic tissues. (A) Representative images of PLAU protein in PDAC and control tissues by IHC staining. Bars = 200 μm. (B) Quantitative results of PLAU protein in PDACs and controls, **** p < 0.0001. (C) Correlation between PLAU protein expression in PDAC and tumor differentiation status of patients, ** p < 0.01. (D) Correlation between PLAU protein expression in PDAC and lymph node metastatic status of patients, * p < 0.05.

Article Snippet: Immunohistochemical staining (IHC) was performed using an antibody against PLAU (1:500 dilution, #17968-1-AP, Proteintech, Wuhan, China).

Techniques: Expressing, Control, Immunohistochemistry

Stellettin B regulated the expression levels in the PI3K/AKT/mTOR signaling pathway. Western blotting analysis was employed to analyze the expressions levels of p -FAK, p -PI3K, p -AKT, and p -mTOR in HA22T and HepG2 cells treated with Stellettin B. Zero refers to cells treated with DMSO vehicle as a control. β -Actin was used as the internal control.

Journal: International Journal of Cell Biology

Article Title: Stellettin B Isolated from Stelletta Sp. Reduces Migration and Invasion of Hepatocellular Carcinoma Cells through Reducing Activation of the MAPKs and FAK/PI3K/AKT/mTOR Signaling Pathways

doi: 10.1155/2022/4416611

Figure Lengend Snippet: Stellettin B regulated the expression levels in the PI3K/AKT/mTOR signaling pathway. Western blotting analysis was employed to analyze the expressions levels of p -FAK, p -PI3K, p -AKT, and p -mTOR in HA22T and HepG2 cells treated with Stellettin B. Zero refers to cells treated with DMSO vehicle as a control. β -Actin was used as the internal control.

Article Snippet: Rabbit antibodies against human MMP-2, MMP-9, uPA, PI3K, and p -PI3K were obtained from Cell Signaling Technology Inc. (Danvers, MA, USA).

Techniques: Expressing, Western Blot, Control