proteon system Search Results


proteontmxpr36 protein interaction array system  (Bio-Rad)
96
Bio-Rad proteontmxpr36 protein interaction array system
Proteontmxpr36 Protein Interaction Array System, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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proteon manager software  (Bio-Rad)
96
Bio-Rad proteon manager software
Proteon Manager Software, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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proteontm amine coupling kit  (Bio-Rad)
94
Bio-Rad proteontm amine coupling kit
Proteontm Amine Coupling Kit, supplied by Bio-Rad, 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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Average 94 stars, based on 1 article reviews
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glc sensor chip  (Bio-Rad)
94
Bio-Rad glc sensor chip
Glc Sensor Chip, supplied by Bio-Rad, 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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proteon microplate sealing film  (Bio-Rad)
92
Bio-Rad proteon microplate sealing film
( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the <t>ProteOn</t> Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.
Proteon Microplate Sealing Film, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/proteon microplate sealing film/product/Bio-Rad
Average 92 stars, based on 1 article reviews
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proteon nlc sensor chip  (Bio-Rad)
93
Bio-Rad proteon nlc sensor chip
( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the <t>ProteOn</t> Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.
Proteon Nlc Sensor Chip, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/proteon nlc sensor chip/product/Bio-Rad
Average 93 stars, based on 1 article reviews
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glm sensors  (Bio-Rad)
93
Bio-Rad glm sensors
( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the <t>ProteOn</t> Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.
Glm Sensors, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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proteontm glh sensor chip surface  (Bio-Rad)
93
Bio-Rad proteontm glh sensor chip surface
( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the <t>ProteOn</t> Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.
Proteontm Glh Sensor Chip Surface, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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proteon hte sensor chips  (Bio-Rad)
93
Bio-Rad proteon hte sensor chips
( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the <t>ProteOn</t> Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.
Proteon Hte Sensor Chips, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ni sulfate activated proteontm htg sensor chip  (Bio-Rad)
93
Bio-Rad ni sulfate activated proteontm htg sensor chip
( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the <t>ProteOn</t> Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.
Ni Sulfate Activated Proteontm Htg Sensor Chip, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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proteon glycine buffer  (Bio-Rad)
88
Bio-Rad proteon glycine buffer
( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the <t>ProteOn</t> Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.
Proteon Glycine Buffer, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sodium acetate buffer  (Bio-Rad)
93
Bio-Rad sodium acetate buffer
( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the <t>ProteOn</t> Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.
Sodium Acetate Buffer, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the ProteOn Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.

Journal: Biomolecules

Article Title: Identification of Small Molecules Blocking the Pseudomonas aeruginosa Type III Secretion System Protein PcrV

doi: 10.3390/biom11010055

Figure Lengend Snippet: ( A ) Surface plasmon resonance data for compound H1 binding to PcrV at 400, 200 (duplicate), 100, 50, 25, 12.5, 6.25, and 0 µM. ( B ) Equilibrium analysis of compound H1 from binding levels at 45-55 s in A : K D was determined to be 98.3 µM. R max was 71.3 RU, and Chi 2 was 10.0 RU. ( C ) Infection assay with dose-response analysis of compound H1 that protects macrophages from T3SS-mediated P. aeruginosa toxicity (wt): uninfected cells and infection with a pcrV mutant were used as controls, and standard deviation was calculated by Gaussian approximation. ( D ) 1 H NMR relaxation-edited binding experiment showing the aromatic region for compound H1 at 100 µM with (bottom trace) and without 10 µM PcrV (upper trace): equilibrium analysis was performed in the ProteOn Manager software TM (Bio-Rad Laboratories Inc., Hercules, CA, USA). ( E ) Bacterial growth assay where P. aeruginosa was grown in the presence of compound H1 at 200, 100, 50, and 25 µM and OD600 was measured regularly for 8 h: each value represents the mean value of a triplicate; to the control wells, 1% DMSO was added (DMSO). The panels show one representative experiment.

Article Snippet: The plates were sealed (ProteOn Microplate sealing film, Bio-Rad Laboratories Inc., Hercules, CA, USA) when the plate was prepared.

Techniques: SPR Assay, Binding Assay, Infection, Mutagenesis, Standard Deviation, Software, Growth Assay, Control