protease inhibitor cocktail Search Results


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PAD2 and PAD4 affect PGO2330 QS gene expression and production of QS-related virulence factors. PGO2330 (5 × 10 5 CFU/mL) was cultured with rPAD2 or rPAD4 (20 n m ) for 24 h. Following incubation, cells were collected for qPCR analysis and the cell-free media (CFM) was assessed for virulence factor production. a qPCR analysis of lasR , lasI , rhlR , rhlI , and mvfR mRNA expression (normalised to ProC ) of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. b eDNA release, protease production, rhamnolipid release, and pyocyanin production of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. c IL-6 and IL-8 gene expression in HBE cells 3 and 24 h post-incubation with rPAD2, rPAD4 (20 n m ), or P. aeruginosa (PAO1) LPS (10 µg/mL) (positive control). Gene expression was assessed by qPCR and calculated relative to untreated control ( n = 3 biological replicates). d Inhibition of PGO2330 protease activity present in 24 h CFM by protease inhibitor <t>(ProtInh)</t> cocktail. Data were analysed by a paired t test and presented as mean ± SEM; n = 3 biological replicates. e Western blot analysis of rPAD2 or rPAD4 (20 n m ) exposed to 24 h growth PGO2330 CFM for 2 h. f Densitometric analysis of PGO2330 CFM-treated rPADs relative to untreated rPADs (con). Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. SEM, standard error of the mean.
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PAD2 and PAD4 affect PGO2330 QS gene expression and production of QS-related virulence factors. PGO2330 (5 × 10 5 CFU/mL) was cultured with rPAD2 or rPAD4 (20 n m ) for 24 h. Following incubation, cells were collected for qPCR analysis and the cell-free media (CFM) was assessed for virulence factor production. a qPCR analysis of lasR , lasI , rhlR , rhlI , and mvfR mRNA expression (normalised to ProC ) of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. b eDNA release, protease production, rhamnolipid release, and pyocyanin production of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. c IL-6 and IL-8 gene expression in HBE cells 3 and 24 h post-incubation with rPAD2, rPAD4 (20 n m ), or P. aeruginosa (PAO1) LPS (10 µg/mL) (positive control). Gene expression was assessed by qPCR and calculated relative to untreated control ( n = 3 biological replicates). d Inhibition of PGO2330 protease activity present in 24 h CFM by protease inhibitor <t>(ProtInh)</t> cocktail. Data were analysed by a paired t test and presented as mean ± SEM; n = 3 biological replicates. e Western blot analysis of rPAD2 or rPAD4 (20 n m ) exposed to 24 h growth PGO2330 CFM for 2 h. f Densitometric analysis of PGO2330 CFM-treated rPADs relative to untreated rPADs (con). Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. SEM, standard error of the mean.
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PAD2 and PAD4 affect PGO2330 QS gene expression and production of QS-related virulence factors. PGO2330 (5 × 10 5 CFU/mL) was cultured with rPAD2 or rPAD4 (20 n m ) for 24 h. Following incubation, cells were collected for qPCR analysis and the cell-free media (CFM) was assessed for virulence factor production. a qPCR analysis of lasR , lasI , rhlR , rhlI , and mvfR mRNA expression (normalised to ProC ) of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. b eDNA release, protease production, rhamnolipid release, and pyocyanin production of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. c IL-6 and IL-8 gene expression in HBE cells 3 and 24 h post-incubation with rPAD2, rPAD4 (20 n m ), or P. aeruginosa (PAO1) LPS (10 µg/mL) (positive control). Gene expression was assessed by qPCR and calculated relative to untreated control ( n = 3 biological replicates). d Inhibition of PGO2330 protease activity present in 24 h CFM by protease inhibitor <t>(ProtInh)</t> cocktail. Data were analysed by a paired t test and presented as mean ± SEM; n = 3 biological replicates. e Western blot analysis of rPAD2 or rPAD4 (20 n m ) exposed to 24 h growth PGO2330 CFM for 2 h. f Densitometric analysis of PGO2330 CFM-treated rPADs relative to untreated rPADs (con). Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. SEM, standard error of the mean.
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Thermo Fisher cocktail protease inhibitors
Structures of Dicer <t>inhibitors.</t>
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Image Search Results


PAD2 and PAD4 affect PGO2330 QS gene expression and production of QS-related virulence factors. PGO2330 (5 × 10 5 CFU/mL) was cultured with rPAD2 or rPAD4 (20 n m ) for 24 h. Following incubation, cells were collected for qPCR analysis and the cell-free media (CFM) was assessed for virulence factor production. a qPCR analysis of lasR , lasI , rhlR , rhlI , and mvfR mRNA expression (normalised to ProC ) of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. b eDNA release, protease production, rhamnolipid release, and pyocyanin production of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. c IL-6 and IL-8 gene expression in HBE cells 3 and 24 h post-incubation with rPAD2, rPAD4 (20 n m ), or P. aeruginosa (PAO1) LPS (10 µg/mL) (positive control). Gene expression was assessed by qPCR and calculated relative to untreated control ( n = 3 biological replicates). d Inhibition of PGO2330 protease activity present in 24 h CFM by protease inhibitor (ProtInh) cocktail. Data were analysed by a paired t test and presented as mean ± SEM; n = 3 biological replicates. e Western blot analysis of rPAD2 or rPAD4 (20 n m ) exposed to 24 h growth PGO2330 CFM for 2 h. f Densitometric analysis of PGO2330 CFM-treated rPADs relative to untreated rPADs (con). Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. SEM, standard error of the mean.

Journal: Journal of Innate Immunity

Article Title: Inhibition of Pseudomonas aeruginosa Biofilm Formation by Peptidyl-Arginine Deiminases 2 and 4

doi: 10.1159/000550256

Figure Lengend Snippet: PAD2 and PAD4 affect PGO2330 QS gene expression and production of QS-related virulence factors. PGO2330 (5 × 10 5 CFU/mL) was cultured with rPAD2 or rPAD4 (20 n m ) for 24 h. Following incubation, cells were collected for qPCR analysis and the cell-free media (CFM) was assessed for virulence factor production. a qPCR analysis of lasR , lasI , rhlR , rhlI , and mvfR mRNA expression (normalised to ProC ) of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. b eDNA release, protease production, rhamnolipid release, and pyocyanin production of rPAD2- and rPAD4-treated PGO2330 cells, relative to the control. Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. c IL-6 and IL-8 gene expression in HBE cells 3 and 24 h post-incubation with rPAD2, rPAD4 (20 n m ), or P. aeruginosa (PAO1) LPS (10 µg/mL) (positive control). Gene expression was assessed by qPCR and calculated relative to untreated control ( n = 3 biological replicates). d Inhibition of PGO2330 protease activity present in 24 h CFM by protease inhibitor (ProtInh) cocktail. Data were analysed by a paired t test and presented as mean ± SEM; n = 3 biological replicates. e Western blot analysis of rPAD2 or rPAD4 (20 n m ) exposed to 24 h growth PGO2330 CFM for 2 h. f Densitometric analysis of PGO2330 CFM-treated rPADs relative to untreated rPADs (con). Data were analysed by a one-way ANOVA followed by multiple comparison Tukey’s post hoc test and presented as mean ± SEM; n = 5 biological replicates. SEM, standard error of the mean.

Article Snippet: Protease inhibitor (ProtInh) cocktail (ThermoFisher) was used as negative control.

Techniques: Gene Expression, Cell Culture, Incubation, Expressing, Control, Comparison, Positive Control, Inhibition, Activity Assay, Protease Inhibitor, Western Blot

Structures of Dicer inhibitors.

Journal: Methods (San Diego, Calif.)

Article Title: miRNA inhibition by proximity-enabled Dicer inactivation

doi: 10.1016/j.ymeth.2019.05.004

Figure Lengend Snippet: Structures of Dicer inhibitors.

Article Snippet: The cells were gently scratched off the dish and transferred into a tube for centrifugation at 4 °C and 600 g for 10 min. After removing the supernatant, the cells were then lysed with 1 mL of ice-cold lysis buffer (Tris 50 mM, NaCl 150 mM, Triton X-100 1%, SDS 0.1%, pH 7.5) containing the cocktail protease inhibitors (ThermoFisher) using a Branson 2510 sonicator at 4 °C (20 × 10 s, at intervals of 20 s).

Techniques: