multi drug resistant pseudomonas aeruginosa Search Results


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ATCC multi drug resistant burkholderia cepacia
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ATCC multi drug resistant pseudomonas aeruginosa
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ATCC multi drug resistant p aeruginosa atcc 27853
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ATCC multi drug resistant p aeruginose
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ATCC a baumannii atcc baa 1605
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ATCC p aeruginosa atcc baa 2114
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ATCC multi drug resistant mdr p aeruginosa strain pao1
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ATCC multi drug resistant p aeruginosa
The antimicrobial and hemolytic activities of lipidated cyclic γ-AApeptides. The microbial organisms used are E. coli (ATCC 25922), K. pneumoniae (ATCC 13383), P. <t> aeruginosa </t> (ATCC 27853), Methicillin-resistant S. epidermidis (RP62A), Vancomycin-resistant E. faecalis (ATCC 700802), and Methicillin-resistant S. aureus (ATCC 33591). The minimum inhibitory concentration (MIC) is the lowest concentration that completely inhibits growth after 24 h. HC 50 is the concentration causing 50% hemolysis. Pexiganan 8 , 29 and previously reported cyclic γ-AApeptide HW-B-13 22 are included for comparison. YL-36 , the compound with the most potent and broad-spectrum activity, is shaded in grey.
Multi Drug Resistant P Aeruginosa, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Medical Education Partnership Ltd topical antimicrobial therapy
The antimicrobial and hemolytic activities of lipidated cyclic γ-AApeptides. The microbial organisms used are E. coli (ATCC 25922), K. pneumoniae (ATCC 13383), P. <t> aeruginosa </t> (ATCC 27853), Methicillin-resistant S. epidermidis (RP62A), Vancomycin-resistant E. faecalis (ATCC 700802), and Methicillin-resistant S. aureus (ATCC 33591). The minimum inhibitory concentration (MIC) is the lowest concentration that completely inhibits growth after 24 h. HC 50 is the concentration causing 50% hemolysis. Pexiganan 8 , 29 and previously reported cyclic γ-AApeptide HW-B-13 22 are included for comparison. YL-36 , the compound with the most potent and broad-spectrum activity, is shaded in grey.
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The antimicrobial and hemolytic activities of lipidated cyclic γ-AApeptides. The microbial organisms used are E. coli (ATCC 25922), K. pneumoniae (ATCC 13383), P.  aeruginosa  (ATCC 27853), Methicillin-resistant S. epidermidis (RP62A), Vancomycin-resistant E. faecalis (ATCC 700802), and Methicillin-resistant S. aureus (ATCC 33591). The minimum inhibitory concentration (MIC) is the lowest concentration that completely inhibits growth after 24 h. HC 50 is the concentration causing 50% hemolysis. Pexiganan 8 , 29 and previously reported cyclic γ-AApeptide HW-B-13 22 are included for comparison. YL-36 , the compound with the most potent and broad-spectrum activity, is shaded in grey.

Journal: ACS chemical biology

Article Title: Lipidated cyclic γ-AApeptides display both antimicrobial and anti-inflammatory activity

doi: 10.1021/cb4006613

Figure Lengend Snippet: The antimicrobial and hemolytic activities of lipidated cyclic γ-AApeptides. The microbial organisms used are E. coli (ATCC 25922), K. pneumoniae (ATCC 13383), P. aeruginosa (ATCC 27853), Methicillin-resistant S. epidermidis (RP62A), Vancomycin-resistant E. faecalis (ATCC 700802), and Methicillin-resistant S. aureus (ATCC 33591). The minimum inhibitory concentration (MIC) is the lowest concentration that completely inhibits growth after 24 h. HC 50 is the concentration causing 50% hemolysis. Pexiganan 8 , 29 and previously reported cyclic γ-AApeptide HW-B-13 22 are included for comparison. YL-36 , the compound with the most potent and broad-spectrum activity, is shaded in grey.

Article Snippet: 19 , 22 The lipidated cyclic γ-AApeptides were tested for their antimicrobial activity against various microbial organisms including E. coli (ATCC 25922), K. pneumonia (ATCC 13383), multi-drug resistant P. aeruginosa (ATCC 27853), Methicillin-resistant S. epidermidis (MRSE, RP62A), Vancomycin-resistant E. faecalis (ATCC 700802), Methicillin-resistant S. aureus (ATCC 33592).

Techniques: Concentration Assay, Comparison, Activity Assay