formulations against e coli atcc 25922 Search Results


99
ATCC escherichia coli atcc 25923
Escherichia Coli Atcc 25923, 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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99
ATCC compounds 5 8 against e coli strains atcc 25922
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Compounds 5 8 Against E Coli Strains Atcc 25922, 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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99
ATCC escherichia coli castellani and chalmers
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Escherichia Coli Castellani And Chalmers, 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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99
ATCC staphylococcus aureus subsp.aureus rosenbach
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Staphylococcus Aureus Subsp.Aureus Rosenbach, 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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99
ATCC pseudomonas aeruginosa migula
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Pseudomonas Aeruginosa Migula, 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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90
ATCC candida tropicalis berkhout
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Candida Tropicalis Berkhout, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC candida albicans berkhout
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Candida Albicans Berkhout, 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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99
ATCC bacillus cereus frankland and frankland
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Bacillus Cereus Frankland And Frankland, 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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99
ATCC bacillus spizizenii dunlap et al
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Bacillus Spizizenii Dunlap Et Al, 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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99
ATCC enterococcus faecalis schleifer and kilpper-balz
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Enterococcus Faecalis Schleifer And Kilpper Balz, 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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90
ATCC candida glabrata meyer et yarrow
Fluorescence microscopy images of <t>E.</t> <t>coli</t> ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.
Candida Glabrata Meyer Et Yarrow, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Fluorescence microscopy images of E. coli ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Article Title: Design and synthesis of theranostic antibiotic nanodrugs that display enhanced antibacterial activity and luminescence

doi: 10.1073/pnas.1708556114

Figure Lengend Snippet: Fluorescence microscopy images of E. coli ORN 178 incubated with nanoaggregates of compound 5. (A) Merged micrograph of bright-field image and fluorescence image (excitation: 405 nm, power intensity: 0.5%). A 410–463-nm filter (see the shadow band II in G and J) was used to exclude autofluorescence from the bacteria. (B) Closer view showing some unattached nanoparticles and bacteria. (C and D) Enlarged views showing nanoparticles attached to the bacterial cells. (E) Bright-field image of one E. coli bacterium with a nanoaggregate attached. (F) Fluorescence lambda-mode micrograph of the bacterium in E acquired 2 min later (405 nm, power intensity: 0.5%). (G) Fluorescence spectra of two ROIs on the bacterium, ROI1 and ROI2 shown in F. The fluorescence signals from ROI1 are dominated by the nanoaggregate emission. The autofluorescence from the bacteria (480–550 nm) existed in both ROI1 and ROI2, showing as weak shoulders marked by dashed red lines in G. (H) Bright-field micrograph of E. coli ORN 178. (I) Fluorescence lambda-mode image under the excitation of laser (405 nm, power intensity 2.8%) showing autofluorescence from bacteria. (J) Normalized average autofluorescence intensity of all E. coli cells in the observation view. Note that the blue color in A–D is pseudo based on F, whereas the color in F and I is the true color.

Article Snippet: MICs of compounds 5–8 against E. coli strains ATCC 25922 and ORN 178 To test whether the nanoaggregate formulation leads to enhanced antibacterial activities, these nanoaggregates and the corresponding compounds in the soluble form were tested against several strains of E. coli [American Type Culture Collection (ATCC) 25922, ORN 178, and ORN 208].

Techniques: Fluorescence, Microscopy, Incubation, Bacteria

MICs of  compounds 5–8 against E. coli strains ATCC 25922  and ORN 178

Journal: Proceedings of the National Academy of Sciences of the United States of America

Article Title: Design and synthesis of theranostic antibiotic nanodrugs that display enhanced antibacterial activity and luminescence

doi: 10.1073/pnas.1708556114

Figure Lengend Snippet: MICs of compounds 5–8 against E. coli strains ATCC 25922 and ORN 178

Article Snippet: MICs of compounds 5–8 against E. coli strains ATCC 25922 and ORN 178 To test whether the nanoaggregate formulation leads to enhanced antibacterial activities, these nanoaggregates and the corresponding compounds in the soluble form were tested against several strains of E. coli [American Type Culture Collection (ATCC) 25922, ORN 178, and ORN 208].

Techniques: