gen5 2.01.14 data analysis software (Agilent technologies)
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gen5 2.01.14 data analysis software
Gen5 2.01.14 Data Analysis Software, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/gen5+software/pm39163813-220-7-12
Average 90 stars, based on 1 article reviews
Gen5 2.01.14 Data Analysis Software, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/gen5+software/pm39163813-220-7-12
Average 90 stars, based on 1 article reviews
gen5 2.01.14 data analysis software - by Bioz Stars,
2026-09
90/100 stars
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Imaging:Article Title: Anticancer Effects of Spiperone in C57BL/6 Mice with Emphysema and Lung Carcinoma. Article Snippet: The antitumor and antimetastatic activity of dopamine D2 receptor antagonists spiperone was studied in C57BL/6 mice in a model of combined pathology (emphysema and lung cancer).. Emphysema was induced by administration of LPS and cigarette smoke extract.. Lung cancer was induced by injection of Lewis lung carcinoma cells into the lung. Article Title: Fibroblast growth receptor 1 is regulated by G-quadruplex in metastatic breast cancer Article Snippet: Paraffin sectioning at 5μm thickness and H&E staining were conducted by AML laboratories, Inc. (Jacksonville, FL). .. The images of lung sections were obtained by Cytation 5 cell imaging multi-mode reader with Software:Article Title: Anticancer Effects of Spiperone in C57BL/6 Mice with Emphysema and Lung Carcinoma. Article Snippet: The antitumor and antimetastatic activity of dopamine D2 receptor antagonists spiperone was studied in C57BL/6 mice in a model of combined pathology (emphysema and lung cancer).. Emphysema was induced by administration of LPS and cigarette smoke extract.. Lung cancer was induced by injection of Lewis lung carcinoma cells into the lung. Article Title: Macrophage-Induced Pro-Fibrotic Gene Expression in Tubular Cells after Ischemia/Reperfusion Is Paralleled but Not Directly Mediated by C5a/C5aR1 Signaling. Article Snippet: Cell culture supernatants were analyzed for TGF-ß using a human TGF-ß ELISA kit (R&D System , Mi neapolis, MN, USA) f llowing the m nufacturer’s instructions and using a Synergy microplate reader and Gen5 software (BioTek In truments GmbH, Fr edrichshall, Germany). .. Rat plasma samples collected at 10 min, 6 h, 24 h, 3 days, 5 days and 8 weeks after I/R were analyzed for C5a using a rat complement component C5a ELISA kit (NBP2-82137, Novus Biologicals, Centennial, CO, USA) following the manufacturer’s instructions and using a Synergy microplate reader and Article Title: The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy. Article Snippet: Expression was terminated by the addition of doxycycline (Merck; 4.5 μM) at desired time points before cell harvest. .. Assessment of cell viability was performed as previously described [36] with the following specifications: 5,000 cells/well were seeded in 96-well cell culture plates (ViewPlate-96 Black, Perkin Elmer, Massachusetts, USA) and transfected 24 h later using Turbofectin 8.0 for 72 h. Cells were treated with 12.5 μM CCCP or vehicle control DMSO for the last 24 h. 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Article Snippet: Cell culture supernatants were analyzed for TGF-ß using a human TGF-ß ELISA kit (R&D System , Mi neapolis, MN, USA) f llowing the m nufacturer’s instructions and using a Synergy microplate reader and Gen5 software (BioTek In truments GmbH, Fr edrichshall, Germany). .. Rat plasma samples collected at 10 min, 6 h, 24 h, 3 days, 5 days and 8 weeks after I/R were analyzed for C5a using a rat complement component C5a ELISA kit (NBP2-82137, Novus Biologicals, Centennial, CO, USA) following the manufacturer’s instructions and using a Synergy microplate reader and Enzyme-linked Immunosorbent Assay:Article Title: Macrophage-Induced Pro-Fibrotic Gene Expression in Tubular Cells after Ischemia/Reperfusion Is Paralleled but Not Directly Mediated by C5a/C5aR1 Signaling. 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Assessment of cell viability was performed as previously described [36] with the following specifications: 5,000 cells/well were seeded in 96-well cell culture plates (ViewPlate-96 Black, Perkin Elmer, Massachusetts, USA) and transfected 24 h later using Turbofectin 8.0 for 72 h. Cells were treated with 12.5 μM CCCP or vehicle control DMSO for the last 24 h. Afterwards, culture medium was aspirated, cells incubated in fresh medium containing the resazurinbased PrestoBlueTM Cell Viability Reagent (Thermo Fisher Scientific) in a 1:10 ratio under standard culture conditions for 60 min. Fluorescence signals were measured at 535 nm (excitation)/615 nm (emission) using a Synergy HT plate reader and the Transfection:Article Title: The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy. Article Snippet: Expression was terminated by the addition of doxycycline (Merck; 4.5 μM) at desired time points before cell harvest. .. Assessment of cell viability was performed as previously described [36] with the following specifications: 5,000 cells/well were seeded in 96-well cell culture plates (ViewPlate-96 Black, Perkin Elmer, Massachusetts, USA) and transfected 24 h later using Turbofectin 8.0 for 72 h. Cells were treated with 12.5 μM CCCP or vehicle control DMSO for the last 24 h. Afterwards, culture medium was aspirated, cells incubated in fresh medium containing the resazurinbased PrestoBlueTM Cell Viability Reagent (Thermo Fisher Scientific) in a 1:10 ratio under standard culture conditions for 60 min. Fluorescence signals were measured at 535 nm (excitation)/615 nm (emission) using a Synergy HT plate reader and the Control:Article Title: The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy. Article Snippet: Expression was terminated by the addition of doxycycline (Merck; 4.5 μM) at desired time points before cell harvest. .. Assessment of cell viability was performed as previously described [36] with the following specifications: 5,000 cells/well were seeded in 96-well cell culture plates (ViewPlate-96 Black, Perkin Elmer, Massachusetts, USA) and transfected 24 h later using Turbofectin 8.0 for 72 h. Cells were treated with 12.5 μM CCCP or vehicle control DMSO for the last 24 h. Afterwards, culture medium was aspirated, cells incubated in fresh medium containing the resazurinbased PrestoBlueTM Cell Viability Reagent (Thermo Fisher Scientific) in a 1:10 ratio under standard culture conditions for 60 min. Fluorescence signals were measured at 535 nm (excitation)/615 nm (emission) using a Synergy HT plate reader and the Incubation:Article Title: The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy. Article Snippet: Expression was terminated by the addition of doxycycline (Merck; 4.5 μM) at desired time points before cell harvest. .. Assessment of cell viability was performed as previously described [36] with the following specifications: 5,000 cells/well were seeded in 96-well cell culture plates (ViewPlate-96 Black, Perkin Elmer, Massachusetts, USA) and transfected 24 h later using Turbofectin 8.0 for 72 h. Cells were treated with 12.5 μM CCCP or vehicle control DMSO for the last 24 h. Afterwards, culture medium was aspirated, cells incubated in fresh medium containing the resazurinbased PrestoBlueTM Cell Viability Reagent (Thermo Fisher Scientific) in a 1:10 ratio under standard culture conditions for 60 min. Fluorescence signals were measured at 535 nm (excitation)/615 nm (emission) using a Synergy HT plate reader and the Fluorescence:Article Title: The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy. Article Snippet: Expression was terminated by the addition of doxycycline (Merck; 4.5 μM) at desired time points before cell harvest. .. Assessment of cell viability was performed as previously described [36] with the following specifications: 5,000 cells/well were seeded in 96-well cell culture plates (ViewPlate-96 Black, Perkin Elmer, Massachusetts, USA) and transfected 24 h later using Turbofectin 8.0 for 72 h. Cells were treated with 12.5 μM CCCP or vehicle control DMSO for the last 24 h. Afterwards, culture medium was aspirated, cells incubated in fresh medium containing the resazurinbased PrestoBlueTM Cell Viability Reagent (Thermo Fisher Scientific) in a 1:10 ratio under standard culture conditions for 60 min. Fluorescence signals were measured at 535 nm (excitation)/615 nm (emission) using a Synergy HT plate reader and the |