raw 264 7 Search Results


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ATCC raw264 7 cell line
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ATCC murine raw264 7 macrophage cell line atcc sc 6003
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ATCC sc 6004
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Santa Cruz Biotechnology α p65
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ATCC sc 6005
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AMS Biotechnology elucidate raw 264 7 nf kb reporter cell line
Inhibitory action of HG2 and HG4 on LPS or LTA-driven inflammation in murine macrophages: eLUCidate™ Raw 264.7 <t>NF-kB</t> reporter cell line was used to measure the inhibitory action of HG2 and HG4 on LPS ( a ) or LTA ( b ) -mediated inflammation as explained in the Materials and Methods’ section. Data were plotted using GraphPad® Prism 7 software. Results are expressed as means ± standard deviation. Representative images of toxicity assay of peptides ( c ) — ( i ) HG2 and ( ii ) HG4 in G. mellonella 120 h post-treatment with 3x MIC concentrations. The larvae remained alive and without melanisation. Virulence assay of MRSA USA300 in G. mellonella using a lethal dose inoculum of 10 6 CFU/per larvae—( iii ) 24 h post-infection: some larvae were dead and partial melanisation was observed. ( iv ). 48 h post-infection: most larvae were dead and complete melanisation was evident. The experiment was done with three experimental replicates, each containing groups of 10 larvae. d Kaplan–Meier survival curves of G. mellonella infected with a lethal dose (LD 50 ) of S. aureus (2.25 × 10 6 CFU/larvae) and treated with peptides HG2 and HG4 at 1x and 3x MIC concentrations and uninfected larvae treated with peptides in PBS at 3x MIC (placebo showing a 100% larvae survival rate).
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Santa Cruz Biotechnology goat anti er β antibody
Inhibitory action of HG2 and HG4 on LPS or LTA-driven inflammation in murine macrophages: eLUCidate™ Raw 264.7 <t>NF-kB</t> reporter cell line was used to measure the inhibitory action of HG2 and HG4 on LPS ( a ) or LTA ( b ) -mediated inflammation as explained in the Materials and Methods’ section. Data were plotted using GraphPad® Prism 7 software. Results are expressed as means ± standard deviation. Representative images of toxicity assay of peptides ( c ) — ( i ) HG2 and ( ii ) HG4 in G. mellonella 120 h post-treatment with 3x MIC concentrations. The larvae remained alive and without melanisation. Virulence assay of MRSA USA300 in G. mellonella using a lethal dose inoculum of 10 6 CFU/per larvae—( iii ) 24 h post-infection: some larvae were dead and partial melanisation was observed. ( iv ). 48 h post-infection: most larvae were dead and complete melanisation was evident. The experiment was done with three experimental replicates, each containing groups of 10 larvae. d Kaplan–Meier survival curves of G. mellonella infected with a lethal dose (LD 50 ) of S. aureus (2.25 × 10 6 CFU/larvae) and treated with peptides HG2 and HG4 at 1x and 3x MIC concentrations and uninfected larvae treated with peptides in PBS at 3x MIC (placebo showing a 100% larvae survival rate).
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Santa Cruz Biotechnology anti transferrin
Inhibitory action of HG2 and HG4 on LPS or LTA-driven inflammation in murine macrophages: eLUCidate™ Raw 264.7 <t>NF-kB</t> reporter cell line was used to measure the inhibitory action of HG2 and HG4 on LPS ( a ) or LTA ( b ) -mediated inflammation as explained in the Materials and Methods’ section. Data were plotted using GraphPad® Prism 7 software. Results are expressed as means ± standard deviation. Representative images of toxicity assay of peptides ( c ) — ( i ) HG2 and ( ii ) HG4 in G. mellonella 120 h post-treatment with 3x MIC concentrations. The larvae remained alive and without melanisation. Virulence assay of MRSA USA300 in G. mellonella using a lethal dose inoculum of 10 6 CFU/per larvae—( iii ) 24 h post-infection: some larvae were dead and partial melanisation was observed. ( iv ). 48 h post-infection: most larvae were dead and complete melanisation was evident. The experiment was done with three experimental replicates, each containing groups of 10 larvae. d Kaplan–Meier survival curves of G. mellonella infected with a lethal dose (LD 50 ) of S. aureus (2.25 × 10 6 CFU/larvae) and treated with peptides HG2 and HG4 at 1x and 3x MIC concentrations and uninfected larvae treated with peptides in PBS at 3x MIC (placebo showing a 100% larvae survival rate).
Anti Transferrin, supplied by Santa Cruz Biotechnology, 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


Inhibitory action of HG2 and HG4 on LPS or LTA-driven inflammation in murine macrophages: eLUCidate™ Raw 264.7 NF-kB reporter cell line was used to measure the inhibitory action of HG2 and HG4 on LPS ( a ) or LTA ( b ) -mediated inflammation as explained in the Materials and Methods’ section. Data were plotted using GraphPad® Prism 7 software. Results are expressed as means ± standard deviation. Representative images of toxicity assay of peptides ( c ) — ( i ) HG2 and ( ii ) HG4 in G. mellonella 120 h post-treatment with 3x MIC concentrations. The larvae remained alive and without melanisation. Virulence assay of MRSA USA300 in G. mellonella using a lethal dose inoculum of 10 6 CFU/per larvae—( iii ) 24 h post-infection: some larvae were dead and partial melanisation was observed. ( iv ). 48 h post-infection: most larvae were dead and complete melanisation was evident. The experiment was done with three experimental replicates, each containing groups of 10 larvae. d Kaplan–Meier survival curves of G. mellonella infected with a lethal dose (LD 50 ) of S. aureus (2.25 × 10 6 CFU/larvae) and treated with peptides HG2 and HG4 at 1x and 3x MIC concentrations and uninfected larvae treated with peptides in PBS at 3x MIC (placebo showing a 100% larvae survival rate).

Journal: NPJ Biofilms and Microbiomes

Article Title: In silico identification of two peptides with antibacterial activity against multidrug-resistant Staphylococcus aureus

doi: 10.1038/s41522-022-00320-0

Figure Lengend Snippet: Inhibitory action of HG2 and HG4 on LPS or LTA-driven inflammation in murine macrophages: eLUCidate™ Raw 264.7 NF-kB reporter cell line was used to measure the inhibitory action of HG2 and HG4 on LPS ( a ) or LTA ( b ) -mediated inflammation as explained in the Materials and Methods’ section. Data were plotted using GraphPad® Prism 7 software. Results are expressed as means ± standard deviation. Representative images of toxicity assay of peptides ( c ) — ( i ) HG2 and ( ii ) HG4 in G. mellonella 120 h post-treatment with 3x MIC concentrations. The larvae remained alive and without melanisation. Virulence assay of MRSA USA300 in G. mellonella using a lethal dose inoculum of 10 6 CFU/per larvae—( iii ) 24 h post-infection: some larvae were dead and partial melanisation was observed. ( iv ). 48 h post-infection: most larvae were dead and complete melanisation was evident. The experiment was done with three experimental replicates, each containing groups of 10 larvae. d Kaplan–Meier survival curves of G. mellonella infected with a lethal dose (LD 50 ) of S. aureus (2.25 × 10 6 CFU/larvae) and treated with peptides HG2 and HG4 at 1x and 3x MIC concentrations and uninfected larvae treated with peptides in PBS at 3x MIC (placebo showing a 100% larvae survival rate).

Article Snippet: The inhibitory activity of HG2, HG4 and comparator compounds against LPS and LTA was assessed using eLUCidate™ Raw 264.7 NF-kB reporter cell line (AMSBIO) as previously described .

Techniques: Software, Standard Deviation, Infection