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medium s aureus atcc 10390 p aeruginosa atcc 15692 k pneumoniae atcc 51503 a baumannii atcc baa 1605 asp 1 ![]() Medium S Aureus Atcc 10390 P Aeruginosa Atcc 15692 K Pneumoniae Atcc 51503 A Baumannii Atcc Baa 1605 Asp 1, 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 https://www.bioz.com/result/medium s aureus atcc 10390 p aeruginosa atcc 15692 k pneumoniae atcc 51503 a baumannii atcc baa 1605 asp 1/product/ATCC Average 99 stars, based on 1 article reviews
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Image Search Results
Journal: Molecules (Basel, Switzerland)
Article Title: Whole-Genome Analysis of Acinetobacter baumannii Strain AB43 Containing a Type I-Fb CRISPR-Cas System: Insights into the Relationship with Drug Resistance.
doi: 10.3390/molecules27175665
Figure Lengend Snippet: Figure 2. Basic information of the Acinetobacter baumannii strain AB43 chromosome. The ring diagram shows the comparison of three A. baumannii strain (AB43, ATCC19606, ATCC17978) chromosomes containing (or not containing) different CRISPR-Cas systems. AB43 contains type I-Fb CRISPR-Cas system, ATCC19606 contains type I-Fa CRISPR-Cas system, ATCC17978 did not contain CRISPR-Cas system. Rings from inside to outside: (1) the G + C content; (2) the GC skew; green and purple represent the GC skew (+) and GC skew (−), respectively; (3) A. baumannii ATCC19606 chromosome; (4) A. baumannii ATCC17978 chromosome; (5) clinical isolate A. baumannii AB43 chromosome. The genes associated with drug resistance and the CRISPR-Cas system in A. baumannii AB43 were marked in the figure. The AB43 CRISPR-Cas system is composed of cas genes, leader sequences, and CRISPR array. Type I system signature gene, cas3, is shown (orange). CRISPR arrays are composed of repeats (blue rectangle) and spacers (colored diamond). These repeats are separated by unique spacers.
Article Snippet:
Techniques: Comparison, CRISPR
Journal: PLOS ONE
Article Title: Differential activation of NLRP3 inflammasome by Acinetobacter baumannii strains
doi: 10.1371/journal.pone.0277019
Figure Lengend Snippet: (A) The survival of C57BL/6 mice following infection by three different strains of A . baumannii (i.p. 2x10 7 CFU/mouse). The level of (B) bacteraemia and (C) bacteria dissemination to different organs at 16–20 hours post infection was quantified. (D) Serum levels of IL-18 and IL-1β in C57BL/6 mice post 16–20 hours intraperitoneal A . baumannii infection. Data were collected from at least three independent experiments, n = 11 (ATCC 19606 and 17978) and n = 13 (ATCC BAA 1605). (b, c, d) data are shown as mean ± SEM. *, Log-rank survival and one-way ANOVA statistical tests were performed. P < 0.05, **, P < 0.01, ***, P < 0.001.
Article Snippet: C57BL/6J/ ANU mice were infected with 2x10 7 CFU/mouse A .
Techniques: Infection, Bacteria
Journal: PLOS ONE
Article Title: Differential activation of NLRP3 inflammasome by Acinetobacter baumannii strains
doi: 10.1371/journal.pone.0277019
Figure Lengend Snippet: (A) ELISA of IL-1β levels produced by mouse BMDM after infection m.o.i. 10 of A . baumannii infection for 12 hours. mean ± SEM. N = 8 per ATCC strains and n = 4 for the clinical isolates (B) Representative western blot image of caspase-1, caspase-11, and GSDMD post infection with different A . baumannii strains. (C) Western blot densitometry quantification normalised to GAPDH and compared to mock. n = 2 per isolates. Unpaired t-test statistical tests were performed mean ± SEM. *, P < 0.05, **, P < 0.01, ***, P < 0.001.
Article Snippet: C57BL/6J/ ANU mice were infected with 2x10 7 CFU/mouse A .
Techniques: Enzyme-linked Immunosorbent Assay, Produced, Infection, Western Blot
Journal: PLOS ONE
Article Title: Differential activation of NLRP3 inflammasome by Acinetobacter baumannii strains
doi: 10.1371/journal.pone.0277019
Figure Lengend Snippet: (A) Representative image of wild-type mouse BMDM cell death post m.o.i. 10 of A. baumannii infection for 24 hours with Hoechst (blue) and Zombie aqua (red) staining. Brightfield staining was included (top panel) (B) Densitometry quantification of the Hoechst and Zombie aqua staining from 5 random field per samples. N = 3 biological replicates per sample. Two-tailed t-tests was performed (C) Representative image and densitometry quantification of A549 cell death post A . baumannii infection at m.o.i. 80 for 24 hours, scale bar: 20 μm. N = 4 per strain. Unpaired t-tests were performed. All data are shown as mean ± SEM. *, P < 0.05, **, P < 0.01, ***, P < 0.001.
Article Snippet: C57BL/6J/ ANU mice were infected with 2x10 7 CFU/mouse A .
Techniques: Infection, Staining, Two Tailed Test